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Review on the effects of exposure to spilledoils on human healthFrancisco Aguilera,a,b,c Josefina Méndez,b Eduardo Pásaroa andBlanca Laffona*
ABSTRACT: Harmful effects of oil spills on diverse flora and fauna species have been extensively studied. Nevertheless, only afew studies have been compiled in the literature dealing with the repercussions of oil exposure on human health; most of themhave focused on acute effects and psychological symptoms. The objective of this work was to gather all these studies and toanalyze the possible consequences of this kind of complex exposure in the different aspects of human health. Studies found onthis topic were related to the disasters of the Exxon Valdez, Braer, Sea Empress, Nakhodka, Erika, Prestige and Tasman Spirit oiltankers. The majority of them were cross-sectional; many did not include control groups. Acute effects were evaluated takinginto account vegetative-nervous symptoms, skin and mucous irritations, and also psychological effects. Genotoxic damageand endocrine alterations were assessed only in individuals exposed to oil from Prestige. The results of the reviewed articlesclearly support the need for biomonitoring human populations exposed to spilled oils, especially those individuals involved inthe cleanup, in order to evaluate not only the possible immediate consequences for their health but also the medium- andlong-term effects, and the effectiveness of the protective devices used. Copyright © 2010 John Wiley & Sons, Ltd.
Keywords: acute toxicity; endocrine toxicity; epidemiological studies; genotoxic effects; human health; oil spills; psychologicaleffects
INTRODUCTION AND BACKGROUND
Since the industrial revolution took place in the eighteenthcentury, the use of fossil fuels, especially petroleum derivatives,has continually increased. It requires their transport from the plat-forms where they are extracted around the world, usually alongsea routes in big tankers. The bad state of a considerable numberof these, added to the fact that many are still monohull, has led tothe high number of accidental spills that have occurred in recentdecades.
In the last five decades approximately 38 accidents involvingsupertankers have taken place, affecting the coasts of differentcountries (International Tankers Owners Pollution FederationLimited; http://www.itopf.com/information-services/data-and-statistics/statistics/index.html#noha/). The major oil spills haveoccurred in western and Mediterranean Europe, as well as inNorth Africa; these regions have experienced 13 of the 20 majorspills. In this respect and considering the high population densityof these geographical areas, they have major interest from theepidemiological point of view.
The main ecosystem constituents affected by the spills are gen-erally seaside flora and some fauna such as birds and bivalvemollusks. Nevertheless, when a big spill occurs there is usually alarge group of volunteers, in general local inhabitants, who mobi-lize and take part in the cleanup work to minimize the impact ofthe spill on the natural and economic resources and recover thecoastal environment as soon as possible. These individuals con-stitute an exposed population whose health may be potentiallyaffected by the noxious properties of the oil.
Harmful effects of oil spills on diverse marine species, espe-cially birds and marine invertebrates, have been extensively
studied. It is enough to type the name of any sunken oil tanker(e.g. Exxon Valdez, Nakhodka, Erika, Urquiola, Braer, Sea Empress,Prestige) into a bibliographic search engine (e.g. PubMed) andmany studies on the impact of the spill on coastal ecosystemsand the contamination and recovery are obtained. Nevertheless,there are only a few studies focused on the repercussions of oilexposure for human health. Most of them are related to acuteeffects and psychological symptoms. Table 1 displays a summaryof the main characteristics of those oil spills for which epidemio-logical studies on the effects on human health have appeared inthe literature.
The objective of this manuscript is to review the studies on theeffects of oil exposure on human health as a result of accidentsinvolving supertankers. Studies were classified according to thetype of effect analyzed into acute toxic and psychological effectsor genotoxic and endocrine effects; also a section compilingsome in vitro works and studies on the bioaccumulationand transference of oil compounds in the food chain isincluded.
*Correspondence to: B. Laffon, Toxicology Unit, University of A Coruña, Edificio deServicios Centrales de Investigación, Campus Elviña s/n, 15071-A Coruña, Spain.E-mail: [email protected]
aUnidad de Toxicología, Dpto. Psicobiología, Universidad de A Coruña, España
bDpto. Biología Celular y Molecular, Universidad de A Coruña, España
cCarrera de Tecnología Médica, Facultad de Medicina, Universidad de Valparaíso,Chile
Review
Received: 11 January 2010, Revised: 25 February 2010, Accepted: 26 February 2010 Published online in Wiley InterScience: 14 April 2010
(www.interscience.wiley.com) DOI 10.1002/jat.1521
291
J. Appl. Toxicol. 2010; 30: 291–301 Copyright © 2010 John Wiley & Sons, Ltd.
IN VITRO STUDIES AND STUDIES ON THEEFFECTS CAUSED BY TRANSFERENCE TO THEFOOD CHAIN
Table 2 displays a summary of the studies included in this section.All of them analyzed effects induced by oil spilled from Erika.Amat-Bronnert et al. (2007) performed an in vitro study in twohuman cell lines, one from hepatoma and another one frombronchial epithelium, treated with an Erika fuel extract. DNAadducts performed by 32P-postlabelling method were onlydetected in hepatoma cells, indicating biotransformation viacytochrome P450 (CYP) 1A2 and 1B1 since the two cell lines donot possess the same metabolic system (hepatoma cells exhibit awide spectrum of metabolic enzymes while bronchial cells donot). Moreover, western blot and densitometry quantificationshowed that exposure to the fuel extract induced some metabo-lizing enzymes such as CYP 1A2, cyclooxygenase 2 and5-lipooxygenase; the latter two are involved in carcinogenic pro-cesses. In epithelial bronchial cells induction of leucotriene B4,a mediator of inflammation, was revealed by inmmunoassay.These results acquire special importance with regard to humanhealth, since inhalation is one of the most representative ways ofabsorbing fuel compounds.
Lemiere et al. (2005) carried out a study to determine thepotential genotoxic risk for consumers of marine food contami-nated with polycyclic aromatic hydrocarbons (PAH) comingfrom oil spills. Mussels (Mytilus sp.) contaminated with Erika oilwere collected and provided daily to rats over periods of 2 and4 weeks. The DNA damage was measured by the single-cell gelelectrophoresis (comet) assay in hepatic, bone marrow andblood cells. While no evidence of genotoxicity was observed inthe peripheral blood samples, significant increases in DNAdamage were observed in the liver and the bone marrow of rats(P < 0.001). The intensity of the DNA damage increased with thePAH contamination level of the mussels. Therefore, this studydemonstrated that oil-contaminated food can cause genotoxicdamage in consumers. Also, it showed that mussels, oftenpresent in the human diet especially in coastal producerregions, carry pollutants in a bioavailable form when contami-nated with oil.
A similar study in rats fed with Erika oil-contaminatedmussels (Mytilus edulis) was performed by Chaty et al. (2008). Ratswere fed for 2 days and CYP 1A1 mRNA expression andethoxyresorufin-O-deethylase (EROD) catalytic activity were ana-lyzed by RT-PCR and a fluorimetric method, respectively. Resultsobtained showed the transient induction of CYP 1A1 mRNA andEROD activity, which reached a maximum after 12 h, returning tobasal levels within 36 h.
The studies presented in this section show evidence for thebioaccumulation of oil compounds and their transference tothe food chain in oil-contaminated marine food, and demonstratethe induction of DNA damage by the products generated bymetabolic enzyme activity transforming many polluting agentsinto even more toxic intermediaries. In this regard, Bro-Rasmussen(1996) indicated that toxic chemicals at low concentrations willnot immediately kill humans; however, depending on their poten-tial to bioconcentrate when climbing the food chain, persistentchemicals may create a human hazard in the case of chronicingestion. For this reason, in vitro and in vivo studies that considernot only bioaccumulation ability, but also the time that the pol-lutants stay in the organisms and the transference rate throughthe different links of the food chain, must be performed, and alsostudies on the optimal way to decontaminate oil-exposed organ-isms to make them safe for human consumption.
EPIDEMIOLOGICAL STUDIES ON ACUTETOXIC AND PSYCHOLOGICAL EFFECTS, ANDSTUDIES ON POTENTIAL TOXICOLOGICALRISK ASSESSMENT
A summary of the studies included in this section is shown inTable 3.
Exxon Valdez
The first oil spill for which studies on the effects on human healthare collected in the literature is the one from Exxon Valdez.Although a variety of studies exist on the ecological impact of thisspill, only a few consider the psychological, psychiatric and socialeffects.
Palinkas et al. (1992) assessed the levels of depressive symp-tomathology between two groups, one of indigenous people(N = 188) and another one of Euro-Americans (N = 371), all ofthem residents in 13 communities of Alaska (11 in the regiondirectly exposed to the oil spill itself and two control communi-ties). The results of these authors suggested that cultural differ-ences played an important role in the perception of thepsychological damage produced by this disaster, which wasrelated to the cleaning work in which the people were involvedand also the damage to fishing grounds, the main sustenance ofthese communities. The group of Euro-Americans showed acertain moderating effect of the damage in relation to familiarsupport; however, this factor did not significantly influence in theindigenous groups. These results emphasize the role of culturaldifferences in the perception of and capacity to overcome thepsychological impact.
Table 1. Oil spills for which epidemiological studies on the effects on human health were reported (ordered by spill size)
Ship name Date Location Spill size (t)
MV Braer 5 January 1993 Southwest Shetland islands, UK 85,000Sea Empress 15 February 1996 Milford Haven, UK 72,000Prestige 19 November 2002 Galicia, Spain 63,000Exxon Valdez 24 March 1989 Bligh ref, Prince William, Alaska, USA 37,000Tasman Spirit 26 July 2003 Karachi, Pakistan 37,000Erika 12 December 1999 South Penmarch, Brittany, France 20,000Nakhodka 2 January 1997 Northeast Oki Island, Sea of Japan, Japan >6,000
292
F. Aguilera et al.
J. App. Toxicol. 2010; 30: 291–301www.interscience.wiley.com/journal/jatwww.interscience.wiley.com/journal/jat Copyright © 2010 John Wiley & Sons, Ltd.
Later, the same authors (Palinkas et al., 1993) as a result of thissame disaster examined the relationship between exposure andsubsequent cleanup efforts and the prevalence of generalizedanxiety disorder, post-traumatic stress disorder (PTSD) anddepressive symptoms in 13 communities of Alaska. They per-formed a community survey of 599 men and women approxi-mately 1 year after the spill. Prevalences of 20.2 and 9.4% werefound for the generalized anxiety disorder and PTSD, respec-tively. Also, the prevalence of depression scale scores above 16and 18 was 16.6 and 14.2%, respectively. For all the parametersanalyzed, exposed individuals showed scores several timeshigher than unexposed individuals Women were particularly vul-nerable to the effects of exposure to the oil spill and cleanupactivities on the prevalence of generalized anxiety disorder (b =0.22, P < 0.0001; odds ratio = 1.43, 95% CI 1.23–1.67), PTSD (b =0.19, P < 0.001; odds ratio = 1.40, 95% CI = 1.15–1.69) and CES-DScale scores of 18 and above (b = 0.17, P < 0.001; odds ratio = 1.35,95% CI = 1.13–1.60). The authors suggest, on the basis of theirresults, improving the mental health care of disaster victims, par-ticularly in primary care settings.
Gill and Picou (1998) monitored the impact of Exxon Valdez spillon the affected populations by means of a 4-year (1989–1992)longitudinal study in which they applied a survey on social dis-ruption and psychological stress, using random-sampling strate-gies, personal interviews and control communities. Dataobtained revealed the chronic nature of stress. Out-migrationexpectations and desires increased from 1989 to 1991. Socialdisruption was reported by a high proportion of residents in1989, but had declined to just over half in 1991. High levels ofevent-related psychological stress were found in 1989 and 1990but they diminished in the following two years.
Finally, Palinkas et al. (2004) confirmed the prevalence of PTSDassociated with ethnic differences. They reported high levels ofsocial disruption one year after this disaster, in both ethnicgroups (indigenous Alaskan and Euro-Americans). However, lowlevel family support, participation in spill cleanup activities and adecline in subsistence activities were significantly associatedwith PTSD in indigenous Alaskan, but not in Euro-Americans.
MV Braer
Campbell et al. (1993) performed a cross-sectional study in whicha population of individuals exposed to MV Braer oil spill (N = 420)was compared with a control group (N = 92), from Hillswick,95 km north of the incident. They compiled information ondemographic details, smoking and alcohol consumption, percep-tion of health, peak expiratory flow, hematology, liver and renalfunction tests, and blood and urine toxicology. Their resultsshowed that, during the first and second day after the spill, thepopulation reported mainly headaches, irritation of the throatand itchy eyes. The authors did not find significant differencesbetween both groups for any of the biological markers. Takingthese results together, only anecdotal reports of certain acutesymptoms could be confirmed.
Later, the same authors reported longer-term effects in thesame populations (344 exposed individuals and 77 controls;Campbell et al., 1994). Among exposed people, 7% perceivedtheir health to be poor compared with none of the controls (c2 =8.05, d.f. = 3, P < 0.05). Comparison of the symptoms of exposedpeople in the 2 weeks before with their presence immediatelyafter the incident showed more tiredness and fever, and fewerthroat, skin and eye irritations, and headaches (odds ratio = 1.86,
Tab
le2.
Invi
tro
stud
ies
and
stud
ies
onth
eeff
ects
caus
edby
tran
sfer
ence
toth
efo
odch
ain
(inor
der
ofth
ech
rono
logy
ofth
esp
ills)
Acc
iden
t–r
efer
ence
Stu
dy
char
acte
rist
ics
Met
ho
ds
Resu
lts
Erik
a–
Am
at-B
ron
ner
tet
al.(
2007
)In
vitr
og
eno
toxi
city
of
anEr
ika
fuel
extr
act
inh
um
anep
ith
elia
lbro
nch
ialc
ells
and
hu
man
hep
ato
ma
cells
DN
Aad
du
cts.
CY
P1A
1,1A
2,1B
1,2C
9,C
OX
1,C
OX
2an
d5-
LOX
pro
tein
exp
ress
ion
.LT
B4
and
PGE2
det
ecti
on
Ad
du
cts
form
atio
nan
din
du
ctio
no
fC
YP
1A2,
CO
X2
and
5-LO
Xin
hep
ato
ma
cells
.Fo
rmat
ion
of
LTB
4in
bro
nch
ialc
ells
Erik
a–
Lem
iere
etal
.(20
05)
Gen
oto
xici
tyas
soci
ated
wit
hEr
ika
oil-
con
tam
inat
edm
uss
els
con
sum
pti
on
inra
tsfe
dd
aily
for
2an
d4
wee
ks
Co
met
assa
yin
hep
atic
cells
,bo
ne
mar
row
and
blo
od
cells
Do
se–e
ffec
t–ti
me
rela
tio
nsh
ipin
hep
atic
and
bo
ne
mar
row
cells
.N
oef
fect
inb
loo
dce
llsEr
ika
–C
hat
yet
al.(
2008
)C
YP
1A1
ind
uct
ion
asso
ciat
edw
ith
Erik
ao
il-co
nta
min
ated
mu
ssel
sco
nsu
mp
tio
nin
rats
fed
for
2d
ays
CY
P1A
1m
RNA
exp
ress
ion
and
ERO
Dca
taly
tic
acti
vity
inliv
erC
YP
1A1
mRN
Aan
dER
OD
acti
vity
tran
sien
tin
du
ctio
n
COX
,cyc
loox
ygen
ase;
CYP
,cyt
ochr
ome
P450
;ERO
D,e
thox
yres
orufi
n-O
-de-
ethy
lase
;LO
X,l
ipoo
xyge
nase
;LT,
leuc
otrie
ne;P
G,p
rost
agla
ndin
e.
293
Effects of exposure to spilled oils on human health
J. App. Toxicol. 2010; 30: 291–301 www.interscience.wiley.com/journal/jatwww.interscience.wiley.com/journal/jatCopyright © 2010 John Wiley & Sons, Ltd.
Tab
le3.
Epid
emio
logi
cals
tudi
eson
acut
eto
xic
and
psy
chol
ogic
aleff
ects
,and
stud
ies
onp
oten
tialt
oxic
olog
ical
risk
asse
ssm
ent
(ord
ered
byth
ech
rono
logy
ofth
esp
ills)
Acc
iden
t–
refe
ren
ceSt
ud
ych
arac
teri
stic
sM
eth
od
sRe
sult
s
Exxo
nVa
ldez
–Pa
linka
set
al.(
1992
)C
ross
-sec
tio
nal
.Et
hn
icd
iffer
ence
sin
stre
ss,c
op
ing,
and
dep
ress
ive
sym
pto
ms
inin
dig
eno
us
peo
ple
(N=
188)
and
Euro
-Am
eric
ans
(N=
371)
CES
-Dsc
ale
Leve
lof
exp
osu
resi
gn
ifica
ntl
yas
soci
ated
wit
hC
ES-D
sco
res
inb
oth
gro
up
s.In
dig
eno
us
peo
ple
had
sig
nifi
can
tly
hig
her
mea
nd
epre
ssiv
esy
mp
tom
sco
re.
InEu
ro-A
mer
ican
sp
erce
ived
fam
ilysu
pp
ort
was
am
od
erat
or
of
effe
cts
of
exp
osu
reo
nd
epre
ssiv
esy
mp
tom
s
Exxo
nVa
ldez
–Pa
linka
set
al.(
1993
)C
ross
-sec
tio
nal
,1ye
araf
ter
the
spill
.C
om
mu
nit
yp
atte
rns
of
psy
chia
tric
-dis
ord
ers
inex
po
sed
(N=
437)
and
con
tro
ls(N
=16
2)
CES
-Dsc
ale.
Qu
esti
on
sfr
om
the
Nat
ion
alIn
stit
ute
of
Men
talH
ealt
hD
iag
no
stic
Inte
rvie
wSc
hed
ule
The
exp
ose
dg
rou
psh
ow
edh
igh
erp
reva
len
ceo
fg
ener
aliz
edan
xiet
yd
iso
rder
and
CES
-Dsc
ore
s�
16an
d18
.W
om
enex
po
sed
wer
ep
arti
cula
rly
vuln
erab
le
Exxo
nVa
ldez
–G
illan
dPi
cou
(199
8)Lo
ng
itu
din
al(4
year
s).
Ch
ron
icco
mm
un
ity
stre
ssan
dso
cial
effe
cts
inre
sid
ents
:19
89(N
=11
8)19
91(N
=22
8)19
92(N
=15
2)an
dco
ntr
ols
:19
89(N
=73
)19
91(N
=10
2)19
92(N
=41
)
Qu
esti
on
nai
res
of
ou
t-m
igra
tio
nd
esir
es,
exp
ecta
tio
ns
and
soci
ald
isru
pti
on
.Ps
ych
olo
gic
alst
ress
by
Even
tsSc
ale
Dat
are
veal
edth
ech
ron
icn
atu
reo
fst
ress
.In
resi
den
tsin
crea
sein
ou
t-m
igra
tio
nex
pec
tati
on
san
dd
esir
es,a
nd
hig
hle
vels
of
even
t-re
late
dp
sych
olo
gic
alst
ress
,dim
inis
hin
gw
ith
tim
e,w
aso
bse
rved
Exxo
nVa
ldez
–Pa
linka
set
al.(
2004
)C
ross
-sec
tio
nal
,1ye
araf
ter
the
spill
.Et
hn
icd
iffer
ence
sin
sym
pto
ms
of
PTSD
inin
dig
eno
us
peo
ple
(N=
188)
and
Euro
-Am
eric
ans
(N=
371)
Mo
difi
edfo
rmo
fVer
sio
nIII
of
the
DIS
Hig
hle
vels
of
soci
ald
isru
pti
on
wer
eas
soci
ated
wit
hPT
SDin
bo
thet
hn
icg
rou
ps.
Low
fam
ilysu
pp
ort
,par
tici
pat
ion
incl
ean
up
acti
viti
es,a
nd
ad
eclin
ein
sub
sist
ence
acti
viti
esw
ere
sig
nifi
can
tly
asso
ciat
edw
ith
PTSD
on
lyin
ind
igen
ou
sp
eop
leM
VBr
aer
–C
amp
bel
let
al.(
1993
)C
ross
-sec
tio
nal
.In
itia
lacu
teef
fect
sin
resi
den
ts(N
=42
0)an
dco
ntr
ols
(N=
92)
Qu
esti
on
nai
res
of
acu
tesy
mp
tom
s,p
eak
exp
irat
ory
flow
,hem
ato
log
y,liv
eran
dre
nal
fun
ctio
nte
sts,
blo
od
and
uri
ne
toxi
colo
gy
Prin
cip
alh
ealt
hef
fect
sar
ose
on
day
s1
and
2(h
ead
ach
es,i
tch
yey
es,a
nd
thro
atir
rita
tio
n).
No
sig
nifi
can
td
iffer
ence
sb
etw
een
exp
ose
dan
dco
ntr
ols
wer
efo
un
dfo
ran
yo
fth
eb
iolo
gic
alm
arke
rs.
Toxi
colo
gic
alst
ud
ies
did
no
tsh
ow
any
exp
osu
reth
atar
ekn
ow
nto
affe
cth
um
anh
ealt
hM
VBr
aer
–C
amp
bel
let
al.(
1994
)C
ross
-sec
tio
nal
.Fo
llow
up
afte
r6
mo
nth
so
fac
ute
effe
cts
inre
sid
ents
(N=
344)
and
con
tro
ls(N
=77
)
Gen
eral
hea
lth
qu
esti
on
nai
re.
Peak
exp
irat
ory
flow
,uri
ne
anal
ysis
,h
emat
olo
gy,
and
liver
and
ren
alfu
nct
ion
test
s
The
mea
ng
ener
alh
ealt
hq
ues
tio
nn
aire
sco
reo
fex
po
sed
was
sig
nifi
can
tly
gre
ater
than
that
of
con
tro
ls.
Exp
ose
dh
adg
reat
erov
eral
lsco
res
for
som
atic
sym
pto
ms,
anxi
ety
and
inso
mn
ia,b
ut
no
tfo
rp
erso
nal
dys
fun
ctio
nan
dse
vere
dep
ress
ion
MV
Brae
r–
Cru
m(1
993)
Cro
ss-s
ecti
on
al.
Effe
cto
nre
spir
ato
rytr
act
inch
ildre
nliv
ing
clo
seto
Brae
rsh
ipw
reck
(N=
44at
3d
ays
and
56at
9–12
day
saf
ter
oil
spill
)
Peak
exp
irat
ory
flow
rate
Peak
exp
irat
ory
flow
rate
sw
ere
wit
hin
the
no
rmal
ran
ge
inb
oth
par
tso
fth
est
ud
y,an
dn
od
eter
iora
tio
nw
asse
enov
erth
est
ud
yp
erio
d
Sea
Empr
ess
–Ly
on
set
al.(
1999
)C
ross
-sec
tio
nal
.A
cute
hea
lth
and
psy
cho
log
ical
effe
cts
inex
po
sed
(N=
539)
and
con
tro
ls(N
=55
0)
Qu
esti
on
nai
res
of
acu
tesy
mp
tom
s.H
AD
and
SF-3
6sc
ore
sEx
po
sed
sho
wed
sig
nifi
can
tly
hig
her
anxi
ety
and
dep
ress
ion
sco
res,
wo
rse
men
talh
ealt
han
dse
lf-re
po
rted
hea
dac
he
and
sore
eyes
and
thro
at
Sea
Empr
ess
–G
alla
cher
etal
.(2
007)
Cro
ss-s
ecti
on
al.
Acu
tesy
mp
tom
ath
olo
gy
attr
ibu
tab
leto
psy
cho
log
ical
exp
osu
rein
exp
ose
d(N
=79
4)an
dco
ntr
ols
(N=
791)
Qu
esti
on
nai
res
of
acu
teto
xic
and
no
n-t
oxic
sym
pto
ms
and
Ho
spit
alA
nxi
ety
and
Dep
ress
ion
Scal
e
Perc
eive
dri
skw
asas
soci
ated
wit
hra
ised
anxi
ety
and
no
n-t
oxic
olo
gic
ally
rela
ted
sym
pto
mre
po
rtin
g.To
xic
sym
pto
mre
po
rtin
gw
asas
soci
ated
wit
ho
ilex
po
sure
and
wit
hra
ised
per
ceiv
edri
sk
Nak
hodk
a–
Mo
rita
etal
.(19
99)
Cro
ss-s
ecti
on
al.
Acu
teh
ealt
hp
rob
lem
sin
exp
ose
d(N
=28
2)Q
ues
tio
nn
aire
so
fac
ute
and
toxi
csy
mp
tom
s.Pe
rso
nal
air
sam
ple
rsto
asse
ssca
rcin
og
enic
ben
zen
e,to
luen
ean
dxy
len
e.U
rin
eto
xici
tyle
vels
Leve
lso
fh
ydro
carb
on
sin
air
wer
efa
rb
elo
wth
eo
ccu
pat
ion
alac
cep
tab
lelim
it.
The
pri
nci
pal
com
pla
ints
of
sym
pto
ms
wer
elo
wb
ack
pai
n,h
ead
ach
ean
dsy
mp
tom
so
fey
esan
dth
roat
Erik
a–
Schv
oer
eret
al.
(200
0)C
ross
-sec
tio
nal
.A
cute
hea
lth
effe
cts
inex
po
sed
(N=
3,66
9)Q
ues
tio
nn
aire
san
dte
lep
ho
ne
inte
rvie
ws
on
acu
tesy
mp
tom
sTh
em
ain
des
crib
edac
ute
sym
pto
ms
wer
elu
mb
arp
ain
,mig
rain
e,d
erm
atit
is,
ocu
lar
irri
tati
on
,res
pir
ato
ryp
rob
lem
san
dn
ause
as.
Du
rati
on
of
the
clea
nin
gw
ork
was
iden
tifie
das
risk
fact
or
294
F. Aguilera et al.
J. App. Toxicol. 2010; 30: 291–301www.interscience.wiley.com/journal/jatwww.interscience.wiley.com/journal/jat Copyright © 2010 John Wiley & Sons, Ltd.
Tab
le3.
Con
tinue
d
Acc
iden
t–
refe
ren
ceSt
ud
ych
arac
teri
stic
sM
eth
od
sRe
sult
s
Erik
a–
Baa
rs(2
002)
Pote
nti
alto
xico
log
ical
risk
asse
ssm
ent
for
peo
ple
invo
lved
incl
ean
ing
acti
viti
esan
dfo
rto
uri
sts
Ris
kch
arac
teri
zati
on
so
nth
eb
asis
of
sup
po
siti
on
so
fth
ep
ote
nti
alex
po
sure
du
rin
gcl
ean
ing
and
tou
rist
acti
viti
es
The
risk
for
the
gen
eral
peo
ple
was
limit
ed.
Incr
ease
dri
skfo
rd
evel
op
ing
skin
irri
tati
on
and
der
mat
itis
,an
dve
rylim
ited
risk
for
dev
elo
pin
gsk
intu
mo
rs,w
ere
des
crib
edfo
rp
eop
lew
ho
had
bee
nin
bar
e-h
and
edco
nta
ctw
ith
the
oil
Erik
a–
Do
ret
al.
(200
3)Po
ten
tial
toxi
colo
gic
alri
skas
sess
men
taf
ter
dec
on
tam
inat
ion
of
36b
each
esp
ollu
ted
by
the
Erik
ao
ilsp
illan
dse
ven
con
tro
lbea
ches
Det
erm
inat
ion
of
the
16PA
Hse
lect
edb
yth
eU
SEP
Ain
san
d,w
ater
and
surf
ace
of
rock
s.Se
ven
scen
ario
so
fex
po
sure
for
peo
ple
usi
ng
the
bea
ches
wer
eco
nte
mp
late
d,an
dth
em
ost
con
serv
ativ
eav
aila
ble
toxi
colo
gic
alva
lues
wer
ese
lect
edfo
rco
mp
uti
ng
risk
s
The
san
dan
dw
ater
wer
esl
igh
tly
po
llute
d,w
ith
valu
essi
mila
rto
tho
sefo
un
din
the
con
tro
lbea
ches
.Th
ero
cky
area
sw
ere
still
hig
hly
po
llute
d.
No
leth
alri
skw
asfo
un
dfo
ra
you
ng
child
wh
oh
adac
cid
enta
llyin
ges
ted
asm
allb
allo
ffu
el.
The
life-
lon
gex
cess
risk
sfo
rsk
inca
nce
ran
dfo
ral
loth
erca
nce
rsw
ere
abo
ut
10-5
insc
enar
ios
incl
ud
ing
con
tact
wit
hth
ep
ollu
ted
rock
s.Th
eh
azar
dq
uo
tien
tfo
rte
rato
gen
icef
fect
sw
asve
rysm
all,
exce
pt
insc
enar
ios
wh
ere
pre
gn
ant
wo
men
wo
uld
wal
kam
on
gro
cks
con
tain
ing
hig
hp
ollu
tio
nle
vels
Pres
tige
–Su
arez
etal
.(2
005)
Cro
ss-s
ecti
on
al.
Acu
teh
ealt
hp
rob
lem
sam
on
gsu
bje
cts
invo
lved
inth
ecl
ean
up
op
erat
ion
afte
rth
esp
ill(N
=80
0)
Qu
esti
on
nai
reo
nex
po
sure
con
dit
ion
s,ac
ute
hea
lth
pro
ble
ms,
and
use
of
pro
tect
ive
mat
eria
l
Bir
dcl
ean
ers
acco
un
ted
for
the
hig
hes
tp
reva
len
ceo
fin
juri
es.
Wo
rkin
gm
ore
than
20d
ays
inh
igh
lyp
ollu
ted
area
sw
asas
soci
ated
wit
hin
crea
sed
risk
of
inju
ryin
allw
ork
ers.
Toxi
cef
fect
sw
ere
hig
her
amo
ng
seam
en.
No
seve
red
iso
rder
sw
ere
iden
tifie
dPr
esti
ge–
Car
rasc
oet
al.(
2006
)C
ross
-sec
tio
nal
.A
sso
ciat
ion
bet
wee
nh
ealt
hin
form
atio
n,u
seo
fp
rote
ctiv
ed
evic
esan
do
ccu
rren
ceo
fac
ute
hea
lth
pro
ble
ms
inex
po
sed
(N=
799)
Qu
esti
on
nai
reo
nex
po
sure
con
dit
ion
s,ac
ute
hea
lth
pro
ble
ms,
use
of
pro
tect
ive
mat
eria
lan
dh
ealt
h-p
rote
ctio
nin
form
atio
nre
ceiv
ed
Hea
lth
-pro
tect
ion
bri
efin
gw
asas
soci
ated
wit
hu
seo
fp
rote
ctiv
ed
evic
esan
dcl
oth
ing.
Un
info
rmed
sub
ject
sre
gis
tere
da
sig
nifi
can
tex
cess
risk
of
itch
yey
es,n
ause
a/vo
mit
ing
/diz
zin
ess,
hea
dac
hes
and
thro
atan
dre
spir
ato
ryp
rob
lem
s.Se
amen
,th
em
ost
exp
ose
dg
rou
p,w
ere
the
wo
rst
info
rmed
and
reg
iste
red
the
hig
hes
tfr
equ
ency
of
toxi
colo
gic
alp
rob
lem
sPr
esti
ge–
Zock
etal
.(2
007)
Lon
git
ud
inal
12-2
4m
on
ths
afte
rth
esp
ill.
Ass
oci
atio
nb
etw
een
par
tici
pat
ion
incl
ean
up
wo
rkan
dre
spir
ato
rysy
mp
tom
sin
exp
ose
d(N
=67
80)
Qu
esti
on
nai
res
wit
hq
ual
itat
ive
and
qu
anti
tati
vein
form
atio
no
ncl
ean
up
acti
viti
esan
dre
spir
ato
rysy
mp
tom
s
The
risk
of
LRTS
incr
ease
dw
ith
the
nu
mb
ero
fex
po
sed
day
s,ex
po
sed
ho
urs
per
day
,an
dn
um
ber
of
acti
viti
es.
The
exce
ssri
sko
fLR
TSd
ecre
ased
wh
enm
ore
tim
eh
adel
apse
dsi
nce
last
exp
osu
rePr
esti
ge–
Car
rasc
oet
al.(
2007
)C
ross
-sec
tio
nal
.H
ealt
h-r
elat
edq
ual
ity
of
life
and
men
talh
ealt
hin
resi
den
tsaf
ter
16m
on
ths
(N=
1350
)an
dco
ntr
ols
(N=
1350
)
Qu
esti
on
nai
res
of
per
ceiv
edso
cial
sup
po
rtan
dm
enta
lhea
lth
SF-3
6,G
HQ
-28,
HA
DS
and
GA
DS
The
SF-3
6sh
ow
edco
asta
lres
iden
tsas
hav
ing
alo
wer
likel
iho
od
of
reg
iste
rin
gsu
bo
pti
mal
valu
esin
ph
ysic
alfu
nct
ion
ing
and
bo
dily
pai
n,a
nd
ah
igh
erfr
equ
ency
of
sub
op
tim
alsc
ore
sin
men
talh
ealt
h
Pres
tige
–Sa
bu
ced
oet
al.(
2009
)C
ross
-sec
tio
nal
.Ps
ych
olo
gic
alim
pac
tin
sub
ject
sfr
om
23co
asta
llo
cati
on
sfr
om
thre
ezo
nes
acco
rdin
gto
thei
rp
roxi
mit
yto
the
loca
tio
no
fth
esp
ill(N
=93
8).
Qu
esti
on
nai
res
on
per
ceiv
edin
volv
emen
tan
dso
cial
sup
po
rt,s
atis
fact
ion
wit
hth
efin
anci
alai
dre
ceiv
edan
dso
cial
rela
tio
nsh
ips.
Mo
difi
edve
rsio
no
fth
eC
RI-A
DU
LT.
Sim
plifi
edve
rsio
no
fth
eSC
L-36
Aff
ecte
dsu
bje
cts
rece
ived
ag
oo
dd
ealo
fso
cial
sup
po
rtan
dw
ere
sati
sfied
wit
hth
eec
on
om
icai
dre
ceiv
ed.
Tho
seaf
fect
edw
ith
hig
hsu
pp
ort
and
sati
sfac
tio
nsc
ore
sw
ere
ina
bet
ter
situ
atio
nth
anth
ose
wit
hlo
wsc
ore
s,an
dev
enb
ette
rth
anth
ose
no
taf
fect
ed
Tasm
anSp
irit
–Ja
nju
aet
al.(
2006
)C
ross
-sec
tio
nal
.A
cute
hea
lth
effe
cts
inex
po
sed
resi
den
ts(N
=21
6)an
dco
ntr
ols
livin
g2
km(N
=83
)an
d20
km(N
=10
1)fa
rfr
om
the
coas
tlin
e
Qu
esti
on
nai
res
on
acu
teh
ealt
hsy
mp
tom
san
do
np
erce
pti
on
abo
ut
the
role
of
oil
spill
inp
rod
uci
ng
illh
ealt
h,a
nd
anxi
ou
snes
sab
ou
tth
eef
fect
of
oil
spill
on
hea
lth
Dat
ash
ow
edm
od
erat
e-to
-str
on
gas
soci
atio
ns
bet
wee
nth
eex
po
sed
gro
up
and
the
sym
pto
ms.
Ther
ew
asa
tren
do
fd
ecre
asin
gsy
mp
tom
-sp
ecifi
cp
reva
len
ceo
dd
sra
tio
sw
ith
incr
ease
ind
ista
nce
fro
mth
esp
illsi
teTa
sman
Spir
it–
Kh
urs
hid
etal
.(2
008)
Cro
ssse
ctio
nal
.H
ealt
hp
aram
eter
so
fp
eop
lew
ork
ing
/liv
ing
inth
evi
cin
ity
of
ano
il-p
ollu
ted
bea
ch(N
=10
0)
Hyd
roca
rbo
n/o
rgan
icco
nte
nt
inse
awat
eran
dsa
nd
sam
ple
s.H
emat
olo
gic
alan
db
ioch
emic
alp
aram
eter
s.Li
ver
and
ren
alfu
nct
ion
test
s
Seaw
ater
had
no
trac
eso
fh
ydro
carb
on
con
ten
t.Ly
mp
ho
cyte
and
eosi
no
ph
ille
vels
wer
esl
igh
tly
incr
ease
d.
Ab
ou
t11
peo
ple
had
rais
edSG
PT,b
ut
this
was
no
tsi
gn
ifica
nt
Tasm
anSp
irit
–M
eoet
al.(
2008
)C
ross
sect
ion
al.
Lun
gfu
nct
ion
inex
po
sed
(N=
20)a
nd
con
tro
ls(N
=31
)
Spir
om
etry
Sig
nifi
can
tre
du
ctio
nin
FVC
,FEV
1,FE
F 25–
75%
and
MV
Vin
exp
ose
d.
Lun
gfu
nct
ion
par
amet
ers
wer
eim
pro
ved
wh
enth
esu
bje
cts
wer
ew
ith
dra
wn
fro
mp
ollu
ted
air
envi
ron
men
t
CES
-D,C
ente
rfo
rEp
idem
iolo
gic
Stud
ies
–D
epre
ssio
n;C
RI-A
DU
LT,c
opin
gre
spon
sein
vent
ory;
DIS
,dia
gnos
ticin
terv
iew
sche
dule
;FEF
25–7
5%,f
orce
dex
pira
tory
flow
;FEV
1,fo
rced
exp
irato
ryvo
lum
ein
first
seco
nd;F
VC,f
orce
dvi
tal
cap
acit
y;G
AD
S,G
oldb
erg
anxi
ety
and
dep
ress
ion
scal
e;G
HQ
,gen
eral
heal
thqu
estio
nnai
re;H
AD
S,ho
spita
lan
xiet
yde
pre
ssio
nsc
ale;
LRTS
,low
resp
irato
rytr
act
sym
pto
mat
holo
gy;M
VV,
max
imum
volu
ntar
yve
ntila
tion;
PAH
,p
olyc
yclic
arom
atic
hydr
ocar
bon
s;PT
SD,p
ost-
trau
mat
icst
ress
diso
rder
;SG
PT,s
erum
glut
amic
pyru
vic
tran
sam
inas
e.
295
Effects of exposure to spilled oils on human health
J. App. Toxicol. 2010; 30: 291–301 www.interscience.wiley.com/journal/jatwww.interscience.wiley.com/journal/jatCopyright © 2010 John Wiley & Sons, Ltd.
95% CI 1.19–2.92). The mean general health questionnaire scoreof the exposed subjects was significantly greater than that of thecontrols. The high rate of non-responders among individualsselected to participate in this study was reported (59 of the 215non-responders in the first phase of the study and 16 of the 86non-responders in the second phase were surveyed). The mainreasons for non-responding was not feeling that their health hadbeen affected, not interested in the study or did not think thestudy was useful (Foster et al., 1995).
Crum (1993) performed a cross-sectional study evaluating thepeak expiratory flow rate in two groups of children aged 5–12years who were resident within 5 km of the Braer shipwreck. Thefirst measure was carried out three days after the accident in 44children, and a second one in 56 children between 9 and 12 daysafter the oil spill. The main results showed that the children’speak expiratory flow rates were within the normal range in bothparts of the study, and no deterioration was seen over the studyperiod, even in the children known to have asthma. No significantdifference was observed between the two sets of values (P =0.502, Student’s t test for paired samples).
Sea Empress
In the wake of the Sea Empress oil spill, Lyons et al. (1999) inves-tigated the acute health effects (self-reported physical and psy-chological symptoms) in the residents of the vicinities of theaffected area (Milford Haven, southwest Wales). They designed aretrospective cohort study that included 539 exposed and 550controls. Results obtained, after adjustment by age, sex andsmoking status, allowed the conclusion that the people living inthe exposed areas presented high levels of anxiety and depres-sion scores, worse mental health and self-reported headache(odds ratio = 2.35, 95% CI 1.56–3.55), sore eyes (odds ratio = 1.96,95% CI 1.06–3.62) and sore throat (odds ratio = 1.70, 95% CI1.12–2.60). These last three symptoms were expected from theknown toxicological effects of oil, so the authors suggested adirect health effect in the exposed population.
On the basis that exposure to a complex emergency has asubstantial psychological component, Gallacher et al. (2007) per-formed work in 794 exposed individuals and 791 controls inwhich anxiety, depression and symptom reporting were used asmeasures of the health impact. The main results indicated thatperceived risk was associated with raised anxiety and non-toxicologically related symptom reporting (odds ratio = 2.28, 95%CI 1.57–3.31, P < 0.001), whereas physical exposure to oil wasonly associated with toxicologically related symptom reporting.The authors concluded that psychological exposure was a sub-stantially more sensitive measure of health impact than physicalexposure in relation to psychological outcomes.
Nakhodka
Morita et al. (1999), as a result of the Nakhodka oil spill, conducteda study in 282 people (men and women) who joined in cleanupwork. Interviews on health status and determinations of severalhydrocarbon metabolites in urine were carried out. Their resultswere similar to those from Campbell et al. (1993), showing thatpeople suffered mainly from pains in the lumbar region and legs,headaches and irritation of eyes and throat. The multivariatelogistic regression model was applied to clarify the risk factors ofhaving at least one symptom with several relevant variables.Results showed that being of female gender, the number of
working days on cleanup activities, direct exposure to oil andhistory of hypertension and low back pain were significant riskfactors for the development of symptoms (P < 0.05). In the urineanalyses, only three individuals showed higher levels of hippuricacid (>1.0 g l-1) that had returned to normality four months later.In this study the use of personal air samplers by the cleanupworkers was remarkable. They allowed the determination of theconcentrations of carcinogenic benzene, toluene and xylene inthe environmental air, and their results showed that these levelswere lower than the occupational acceptable limits (10 ppm forbenzene, 100 ppm for toluene and 100 ppm for xylene). Thehighest concentration of suspended particles on any given daywas 0.088 mg m-3, also below the occupational acceptable limit(2 mg m-3).
Erika
Schvoerer et al. (2000) presented a cross-sectional investigationon human health risk assessment as a result of the Erika oil spill in3669 interviewed people, who included cleaning workers andvolunteers. Their results indicated that 7.5% of the individualsexperienced some type of wound and 53% some health problem(30% lumbar pain, 22% migraine, 16% dermatitis). They reportedin a smaller degree ocular irritation (9%), respiratory problems(7%) and nausea (6%). The duration of the cleaning work wasidentified as a risk factor.
Baars (2002) evaluated the health risk for people involved inthe cleaning activities after the Erika oil spill and also for tourists,with an emphasis on the carcinogenic properties of the oil, on thebasis of the known toxicological properties of the oil componentsand assumptions on the levels of exposure during the perfor-mance of different activities. In assessing toxic risks the actualexposure levels were compared with limit values taken from theliterature; in assessing carcinogenic risk the actual exposurelevels were compared with the 1:104 lifetime excess risk of devel-oping tumors. The outcome indicated that the risks for thegeneral population were limited. For people who had been inbare-handed contact with the oil there was increased risk ofdeveloping skin irritation and dermatitis, but these effects werein general reversible, and also that of developing skin tumors,which was very limited due to the short contact time with the oil.
Dor et al. (2003) reported an assessment of human health riskafter decontamination of beaches polluted by the Erika oil. Theydetermined the 16 PAH selected by the US EPA in samples ofsand, water and the surface of rocks from 36 cleaned-pollutedbeaches and seven control beaches, and contemplated sevenpossible scenarios of exposure for people using the beaches intourist activities (children, adults and pregnant women) orworking activities. The life-long excess risk for skin cancer andfor all other cancers was about 10-5 in scenarios including contactwith the polluted rocks. The authors concluded that exposurewas mainly associated with polluted water among children andwith contaminated rocks for adults, and that, despite uncertain-ties, decontaminated beaches did not entail any significanthealth risks and could be opened to the public.
Prestige
As a result of the disaster of the tanker Prestige, densely popu-lated coastal regions of Spain (Galicia, Asturias, Cantabria and theBasque country), as well as the neighboring French coasts, with
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intense activity of extraction of marine resources and tourism,were affected. Several studies were performed after this accidentin order to evaluate the possible human health effects.
Suarez et al. (2005) evaluated the conditions of exposure andthe acute health effects in individuals who participated in thecleanup works in the regions of Asturias and Cantabria (Spain),and the association between these and the type of work. Fourhundred individuals from each region were interviewed. Col-lected data included information on the work performed, use ofprotection devices and acute symptoms. Bird cleaners accountedfor the highest prevalence of lesions (19%, P < 0.001), includingneurovegetative disorders (11.2%, P = 0.169) and low back pain(3.1%, P = 0.281). Working periods longer than 20 days in highlypolluted areas were associated with increased risk of injury in allworkers. A specific analysis restricted to seamen only found astrong and significant association with having worked for morethan 3 days (odds ratio = 14.30 and 11.02 for categories of 3–20days and over 20 days, respectively) and having torn or not wornthe protective suit (odds ratio = 1.20 and 7.79, respectively), butno severe disorders were identified among individuals analyzed.
The same authors reported another study examining the asso-ciation between use of protective devices, frequency of acutehealth problems and health-protection information received by799 exposed individuals, classified according to the tasks per-formed (Carrasco et al., 2006). These authors observed a signifi-cant excess risk of itchy eyes (odds ratio = 2.89; 95% CI 1.21–6.90),nausea/vomiting/dizziness (odds ratio = 2.25; 95% CI 1.17–4.32)and throat and respiratory problems (odds ratio = 2.30; 95% CI1.15–4.61) among uninformed subjects. Furthermore, there wasa noteworthy significant excess risk of headaches (odds ratio =3.86; 95% CI 1.74–8.54) and respiratory problems (odds ratio =2.43; 95% CI 1.02–5.79) among uninformed paid workers.Seamen, the group most exposed to the spilled oil, were theworst informed and registered the highest frequency of toxico-logical problems. Therefore, the authors confirmed the resultsobtained in their previous study and found a significant associa-tion between proper health-protection briefing and use of pro-tective devices and lower frequency of health problems.
Zock et al. (2007) evaluated the prevalence of lower respiratorytract symptoms (LRTS) more than a year after Prestige accident in6780 fishermen who had participated in the cleanup labors(response rate 76%), through questionnaires that included quali-tative and quantitative information. Their results showed thatLRTS was more prevalent in cleanup workers (odds ratio = 1.73;95% CI 1.54–1.94), and that the risk of LRTS increased in relationto the number of exposed days, exposed hours per day andnumber of activities carried out (linear trend, P < 0.0001). Theexcess risk of LRTS decreased with elapsed time since last expo-sure (odds ratio = 2.33, 1.69 and 1.24 for less than 14 months,14–20 months, and more than 20 months, respectively), althoughit was still significant when more than 20 months had elapsed.
Carrasco et al. (2007) performed a new study on the effects ofthe Prestige oil spill on health-related quality of life (HRQoL) andmental health in the affected population, approximately 18months after this disaster, using several questionnaires. The mainresults showed coastal residents as having a lower likelihood ofregistering suboptimal HRQoL values in physical functioning(odds ratio = 0.69; 95% CI 0.54–0.89) and bodily pain (oddsratio = 0.74; 95% CI 0.62–0.91), and a higher frequency of subop-timal scores in mental health (odds ratio = 1.28; 95% CI 1.02–1.58). The authors concluded that, almost one and a half yearsafter the accident, worse HRQoL and mental health levels were
not in evidence among subjects exposed to the spilled oil. Nev-ertheless, a slight impact on the mental health of residents in theaffected areas was suggested by some of the scales applied.
Similar results were obtained by Sabucedo et al. (2009), whoevaluated the psychological impact of Prestige oil spill. Theycarried out a descriptive study that involved 938 men andwomen from 23 localities throughout the Galician coast. Half ofthem were fishermen or workers related to the extraction offishing resources, and the other half were not linked to theseactivities. Questionnaires on different psychological and psycho-social factors were filled in at the time of the accident and oneyear after. The results showed that the affected subjects hadreceived a good deal of social support and were satisfied with theeconomic aid received. In addition, affected individuals with highsupport and satisfaction scores were currently in a better situa-tion than those affected with low scores, and even better thanthose not affected.
Tasman Spirit
Janjua et al. (2006), following the Tasman Spirit shipwreck, con-ducted a study which included an exposed group composed ofadults of both genders living on the affected coastline (N = 216)and two control groups living 2 km (N = 83) and 20 km (N =101),respectively, away from the indicated area. Surveys on acutesymptoms related to eyes, respiratory tract, skin and nervoussystem, as well as consultations of allergies, tobacco consumptionand perceptions on the effect on their health and anxiety abouttheir health effects were performed. Their results showedmoderate-to-strong associations (prevalence odds ratios rangingfrom 2.3 to 37.0) between the exposed group and the symptoms,which decreased with the distance from the spill site, and multiplelinear regression model revealed strong relationship of exposurestatus with the symptoms score (b = 8.24, 95% CI 6.37–10.12).
Khurshid et al. (2008) presented a short-term study in peoplewho were working or living in the vicinity of Karachi beach.Hematological and biochemical parameters were determined,and liver and renal function tests were carried out. They also tookseawater and sand samples and analyzed them for hydrocarbon/organic contents. The results only showed slight rises in the levelsof lymphocytes and eosinophiles. The authors recommendedperforming follow-up studies after oil spills taking samples every3 months for 3–5 years, noting respiratory disorders and anychanges in the skin.
Finally, Meo et al. (2008) assessed, by means of spirometry,lung function and followed up the progression after one year in20 subjects exposed to this oil spill and 31 controls. Subjectsexposed to polluted air had significant reductions in lung func-tion compared with their matched controls (P ranging from 0.001to 0.02 for the different lung function parameters). The reportedimpairment was reversible and lung function parameters wereimproved when the subjects were withdrawn from the pollutedair environment.
In summary, studies performed after Exxon Valdez spill onlyaccounted for psychological effects in the exposed populations.For all the other accidents, there are also studies on acute toxiceffects, and moreover, for the Erika oil spill there are two works onpotential toxicological risk assessment, both concluding thatexposure to pollutants contained in the oil during commonactivities did not entail any significant health risk. Data obtainedin most of these studies indicated that technological disastersthat involve oil spills have acute physical consequences
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that diminish with time and are mainly reversible, and psycho-logical consequences and continuing disruptive and stress-provoking consequences for resident communities. The resultsalso suggested that conflicting definitions of long-term effectsand recovery of the natural environment contributed to commu-nity stress.
EPIDEMIOLOGICAL STUDIES ONGENOTOXICITY AND ENDOCRINE TOXICITY
Table 4 displays a summary of the main characteristics of thesestudies.
Braer
Cole et al. (1997) evaluated the possible genotoxicity as a conse-quence of the Braer tanker oil spill. They used blood samples toassess the primary damage in the DNA (DNA adducts in themononuclear cell fraction by a modified 32P-postlabeling methodand mutations at the hprt locus in T lymphocytes). These authorsdid not obtain any evidence of genotoxicity for either end point,but they proposed several issues to be taken into account in thedesign of biomonitoring studies after oil spills.
Prestige
Laffon et al. (2006) conducted a study to determine the possiblegenotoxic damage associated with the exposure to Prestige oil, in34 volunteers, who worked in autopsies and cleaning of oil-contaminated birds, and 35 controls. Environmental concentra-tions of volatile organic compounds (VOC) in the working roomwere determined. Genotoxicity was evaluated by means ofmicronucleus (MN) test and comet assay, and the possible influ-ence of several DNA repair genetic polymorphisms was also ana-lyzed. Their results showed significantly higher DNA damage (P <0.01), but not cytogenetic damage, in relation to the exposuretime (r = 0.376, P < 0.05), and also certain exposure–genotypeinteractions.
Pérez-Cadahía and colleagues performed a study with theobjective of evaluating the genotoxicity and endocrine toxicityrelated to exposure to Prestige oil during the different cleaninglabors. Exposed individuals were classified into three groups:manual volunteers, hired manual workers and hired workersusing high-pressure water machines. The environmental expo-sure levels of VOC were determined, and different biologicalparameters were measured. Their results were published in dif-ferent papers. In an initial stage (Pérez-Cadahía et al., 2006, 2007),a relatively small population (68 total exposed vs 42 controls) wasanalyzed. The data obtained indicated that the highest levels ofVOC were observed in the volunteer environment and that expo-sure to Prestige oil induced genotoxic damage (tests applied:sister chromatid exchanges (SCE), MN test and comet assay), thecomet assay being the most sensitive test to detect it, and alter-ations in hormonal status (prolactin and cortisol plasma concen-trations, significant decreases with P < 0.01). Also, gender, ageand tobacco smoking influenced the levels of genetic damage,while the effect of using protective devices (clothes and mask)was less noticeable than expected.
Later, they enlarged the study with the aim of checking thevalidity of their previous data, including 180 exposed subjects
and 60 controls. Their results showed significant increases in thelevels of blood heavy metals (aluminum, nickel and lead) andDNA damage, and alterations in the endocrine status of theexposed populations (significantly higher prolactin plasma con-centrations, P < 0.01; Pérez-Cadahía et al., 2008a). They also foundgeneral increases in MN frequency and decreases in the prolifera-tion index in the individuals with longer times of exposure (Pérez-Cadahía et al., 2008b). Moreover, significant influence of severalgenetic polymorphisms in metabolizing enzymes and DNA repairproteins was observed. In addition, their previous resultsshowing the absence of effect of using protective devices wereconfirmed.
Finally, the same authors (Pérez-Cadahía et al., 2008c) investi-gated the relationship between blood levels of heavy metals andgenotoxic or endocrine parameters in the individuals exposed toPrestige oil. Cortisol plasma concentration appeared to be themost sensitive parameter to the effects of metal exposure, since itwas significantly influenced by blood concentrations of alumi-num, nickel (both inversely) and cadmium (positively), and jointlyby aluminum and nickel. On this basis, the authors suggestedplasma levels of cortisol as a potentially relevant biomarker toassess the effects of exposure to heavy metals.
Taking into account the known genotoxic, cancer-provokingand endocrine disrupting properties of many compounds con-tained in the spilled oils, it seems surprising that only for two oilspills (Braer and Prestige) are there studies contemplating theseconsequences for human health in exposed individuals. Theresults obtained in most of these studies provide evidence ofgenotoxicity and alterations in the hormonal status related to theexposure. The only work with negative results (Cole et al., 1997)comprised a relatively small population (26 exposed vs 9 con-trols), and nothing is specified on the participation of theexposed individuals in the cleanup tasks; only their status as resi-dents in the polluted area is mentioned. It seems probable thatdirect participation in the cleanup work involved a higher expo-sure to the oil toxic compounds than that experienced by zoneinhabitants who did not participate in the cleaning.
CONCLUSIONS
Until now there have been 38 large oil spills, but only for seven ofthem have studies on the repercussions of the exposure to spilledoils on human health been performed. Most of these investiga-tions correspond to cross-sectional epidemiological studies thatanalyze acute physical effects or psychological consequences inthe affected people. Some of them do not include a matchedcontrol population, which makes the information provided con-fusing and difficult to interpret. A smaller number of studies arein vitro or in vivo approaches aiming to investigate the effects atthe cellular level and the ability of the oil compounds to be trans-ferred into the food chain and induce damage in consumers;others are focused on biological markers indicative of genotoxi-city and/or endocrine toxicity.
On the occasion of the Prestige oil spill, Porta and Castaño-Vinyals (2003) recommended performing epidemiologicalstudies of exposure to the spilled oil on the medium- and long-term impact on human health. In addition to a first transversalstage, they recommend the monitoring of the exposed popula-tions in a second longitudinal stage. This would allow (i) deter-mination of whether the biomarkers of internal dose, ofbiologically effective dose and of early biological response
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Tab
le4.
Epid
emio
logi
cals
tudi
eson
geno
toxi
city
and
endo
crin
eto
xici
ty(o
rder
edby
the
chro
nolo
gyof
the
spill
s)
Acc
iden
t–
refe
ren
ceSt
ud
ych
arac
teri
stic
sM
eth
od
sR
esu
lts
Brae
r–
Co
leet
al.
(199
7)Lo
ng
itu
din
al.
Gen
oto
xici
tyin
resi
den
ts(N
=26
)an
dco
ntr
ols
(N=
9)at
3sa
mp
ling
tim
es(1
0d
ays,
10w
eeks
and
1ye
araf
ter
the
acci
den
t)
DN
Aad
du
cts
inth
em
on
on
ucl
ear
cell
frac
tio
nan
dfr
e-q
uen
cyo
fh
prt
mu
tati
on
sin
Tly
mp
ho
cyte
sN
oev
iden
ceo
fg
eno
toxi
city
was
ob
tain
edfo
rei
ther
end
po
int
Pres
tige
–La
ffo
net
al.
(200
6)C
ross
-sec
tio
nal
.G
eno
toxi
city
inin
div
idu
als
per
form
ing
auto
psi
esan
dcl
ean
ing
of
oil-
con
tam
inat
edb
ird
s(N
=34
)an
dco
n-
tro
ls(N
=35
)
Envi
ron
men
talV
OC
.C
om
etas
say
and
MN
test
.DN
Are
pai
rg
enet
icp
oly
mo
r-p
his
ms
(XRC
C1,
XRC
C3,
APE
1)
Sig
nifi
can
tin
crea
sein
the
com
etas
say,
bu
tn
ot
inth
eM
Nte
st,r
elat
edto
the
tim
eo
fex
po
sure
.Ex
po
sed
ind
ivid
ual
sca
rryi
ng
XRC
C1-
399G
lno
rA
PE1-
148G
lual
lele
ssh
ow
edin
crea
sed
DN
Ad
amag
ePr
esti
ge–
Pére
z-C
adah
íaet
al.(
2006
)C
ross
-sec
tio
nal
.G
eno
toxi
city
invo
lun
teer
san
dh
ired
wo
rker
sp
arti
ci-
pat
ing
inth
ecl
ean
up
(N=
68)a
nd
con
tro
ls(N
=42
)
Envi
ron
men
talV
OC
.C
om
etas
say,
SCE,
MN
test
Hig
hes
tV
OC
leve
lsin
the
volu
nte
er’s
envi
ron
men
t.Si
gn
ifica
nt
incr
ease
inth
eco
met
assa
yin
exp
ose
din
di-
vid
ual
s.In
fluen
ceo
fse
x,ag
ean
dto
bac
cosm
oki
ng
on
the
gen
oto
xici
tyva
riab
les.
No
effe
cto
fu
sin
gp
rote
ctiv
em
ask
du
rin
gcl
ean
up
lab
ors
Pres
tige
–Pé
rez-
Cad
ahía
etal
.(20
07)
Cro
ss-s
ecti
on
al.
Gen
toxi
city
and
end
ocr
ine
alte
rati
on
sin
volu
nte
ers
and
hir
edw
ork
ers
par
tici
pat
ing
inth
ecl
ean
up
(N=
68)a
nd
con
tro
ls(N
=42
)
Envi
ron
men
talV
OC
.H
eavy
met
als
inb
loo
d(A
l,C
d,N
i,Pb
,Zn
).SC
E.Pr
ola
ctin
and
cort
iso
l.M
etab
olic
gen
etic
po
lym
orp
his
ms
(GST
M1,
GST
T1,
GST
P1)
Hig
hes
tV
OC
leve
lsin
the
volu
nte
er’s
envi
ron
men
t.Si
gn
ifica
nt
incr
ease
inth
ele
vels
of
Al,
Nia
nd
Pb,a
nd
dec
reas
eo
fZ
n,i
nex
po
sed
ind
ivid
ual
s.Si
gn
ifica
nt
incr
ease
inSC
Era
tein
exp
ose
d,in
fluen
ced
by
age,
sex,
smo
kin
gan
dG
STM
1p
oly
mo
rph
ism
.Si
gn
ifica
nt
dec
reas
ein
pro
lact
inan
dco
rtis
oll
evel
sin
exp
ose
dsu
bje
cts
Pres
tige
–Pé
rez-
Cad
ahía
etal
.(2
008a
)
Cro
ss-s
ecti
on
al.
Gen
toxi
city
and
end
ocr
ine
alte
rati
on
sin
volu
nte
ers
and
hir
edw
ork
ers
par
tici
pat
ing
inth
ecl
ean
up
(N=
180)
and
con
tro
ls(N
=60
)
Hea
vym
etal
sin
blo
od
(Al,
Cd,
Ni,
Pb,Z
n).
Co
met
assa
y.Pr
ola
ctin
and
cort
iso
l.M
etab
olic
gen
etic
po
lym
orp
his
ms
(CY
P1A
1,EP
HX
1,G
STM
1,G
STT1
,GST
P1)
Sig
nifi
can
tin
crea
sein
the
leve
lso
fA
l,N
ian
dPb
,an
dd
ecre
ase
of
Zn
,in
exp
ose
din
div
idu
als.
Sig
nifi
can
tin
crea
sein
com
etas
say
and
dec
reas
ein
cort
iso
llev
els
inex
po
sed
ind
ivid
ual
s.H
igh
erD
NA
dam
age
was
rela
ted
toC
YP
1A1
and
EPH
X1
vari
ant
alle
les,
and
low
erD
NA
dam
age
toG
STM
1an
dG
STT1
nu
llg
eno
typ
esPr
esti
ge–
Pére
z-C
adah
íaet
al.
(200
8b)
Cro
ss-s
ecti
on
al.
Gen
toxi
city
invo
lun
teer
san
dh
ired
wo
rker
sp
arti
cip
at-
ing
inth
ecl
ean
up
(N=
159)
and
con
tro
ls(N
=60
)
MN
test
.M
etab
olic
gen
etic
po
lym
orp
his
ms
(CY
P1A
1,C
YP
1B1,
EPH
X1,
GST
M1,
GST
T1,G
STP1
).D
NA
rep
air
gen
etic
po
lym
orp
his
ms
(XRC
C1,
XRC
C3,
XPD
)
Gen
eral
incr
ease
sin
MN
freq
uen
cyan
dd
ecre
ases
inth
ep
rolif
erat
ion
ind
exw
ere
ob
serv
edin
ind
ivid
ual
sw
ith
lon
ger
tim
eo
fex
po
sure
.A
llth
ep
oly
mo
rph
ism
san
alyz
ed,e
xcep
tin
gfo
rC
YP
1B1
and
XRC
C1,
influ
ence
dcy
tog
enet
icd
amag
ele
vels
Pres
tige
–Pé
rez-
Cad
ahía
etal
.(2
008c
)
Cro
ss-s
ecti
on
al.
Rela
tio
nsh
ipb
etw
een
blo
od
con
cen
trat
ion
so
fh
eavy
met
als
and
cyto
gen
etic
and
end
ocr
ine
par
amet
ers
inex
po
sed
by
mea
ns
of
un
ivar
iate
stat
isti
cs(g
ener
allin
ear
mo
del
)(N
=17
9).
Hea
vym
etal
sin
blo
od
(Al,
Cd,
Ni,
Pb,Z
n).
Co
met
assa
y,SC
E,M
Nte
st.
Pro
lact
inan
dco
rtis
ol
Pbw
asre
late
dto
the
com
etas
say.
Co
rtis
olp
lasm
aco
nce
ntr
atio
nw
asin
fluen
ced
by
Al
and
Nii
nver
sely
and
by
Cd
po
siti
vely
.In
wo
men
ther
ew
asa
stro
ng
asso
ciat
ion
bet
wee
nC
dan
dp
rola
ctin
leve
ls
MN
,mic
ronu
cleu
ste
st;S
CE,
sist
erch
rom
atid
exch
ange
s;VO
C,v
olat
ileor
gani
cco
mp
ound
s.
299
Effects of exposure to spilled oils on human health
J. App. Toxicol. 2010; 30: 291–301 www.interscience.wiley.com/journal/jatwww.interscience.wiley.com/journal/jatCopyright © 2010 John Wiley & Sons, Ltd.
remain stable with time or undergo variations; (ii) determinationof certain factors influencing the mentioned biomarkers; and (iii)analysis of the levels of biomarkers or any other factor associatedwith the appearance of a particular illness, subclinical effects orinteresting alterations (physiological, genotoxic, etc.).
Some studies compare the evaluated or estimated exposurelevels with occupational acceptable exposure limits, or use theselimits to calculate the potential toxicological risk. Nevertheless,this comparison is not entirely correct, since the occupationallimits are usually defined for exposures of 8 h/day during a wholeworking life, i.e. considering a chronic exposure. Exposure tospilled oils takes place over several days or some months at themost, involving time periods much shorter than occupationalexposures.
In summary, most of the studies collected in this reviewprovide evidence on the relationship between exposure tospilled oils and the appearance of acute physical, psychological,genotoxic and endocrine effects in the exposed individuals. Con-sidering the relatively high frequency of this kind of environmen-tal disaster, it seems necessary to establish detailed interventionprotocols that include some mechanisms to detect and controlthe possible harmful health effects that exposure can induce,including performing the immediate collection of biologicalsamples from the beginning of the cleanup work, in order toestablish the levels of individual internal exposure effects at theacute and chronic level, especially those related to genotoxicity.This will permit not only determination of the risk that exposuremay involve, but also evaluation of whether protective devicesused by the individuals in each case adequately fulfilled theirfunction, or on the contrary they did not exert the required pro-tection and therefore require to revision of material characteris-tics and improved briefing sessions on their correct use.
Acknowledgments
This work was funded by a grant from the Xunta de Galicia(INCITE08PXIB106155PR). F. Aguilera was supported by a fellow-ship from the Fundación Carolina.
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