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Review Article Role of Obesity in the Risk of Breast Cancer: Lessons from Anthropometry - Hindawi PDF

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HindawiPublishingCorporation JournalofOncology Volume2013,ArticleID906495,19pages http://dx.doi.org/10.1155/2013/906495 Review Article Role of Obesity in the Risk of Breast Cancer: Lessons from Anthropometry AminaAmadou,1PierreHainaut,2andIsabelleRomieu1 1NutritionalEpidemiologyGroup,NutritionandMetabolismSection,InternationalAgencyforResearchonCancer, 150CoursAlbertomas,69372LyonCedex08,France 2InternationalPreventionResearchInstitute,95CoursLafayette,69006Lyon,France CorrespondenceshouldbeaddressedtoIsabelleRomieu;[email protected] Received9October2012;Accepted29November2012 AcademicEditor:DagrunEngeset Copyright©2013AminaAmadouetal. is is an open access article distributed under the Creative Commons Attribution License,whichpermitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperly cited. Anestimated1.38millionnewcasesofbreastcancer(BC)arediagnosedeachyearinwomenworldwide.Ofthese,themajority are categorized as invasive ductal cell carcinoma. Subgroups of BC are frequently distinguished into �ve “intrinsic” subtypes, namely, luminal A, luminal B, normal-like, HER2-positive, and basal-like subtypes. Epidemiological evidence has shown that anthropometricfactorsareimplicatedinBCdevelopment.Overallconsistentpositiveassociationshavebeenobservedbetween highbodymassindex(BMI)andwaist-to-hipratio(WHR)andtheriskofBCamongpostmenopausalwomen,whilecon�icting resultspersistforpremenopausalBC, bothforBMIandforotheranthropometricparametersaswellasacrossethnicgroups. Furthermore,someevidencesuggeststhatbodysize,bodyshape,andweightgainduringchildhoodoradolescencemayplayarole intheriskofBC.Inthispaper,wedescribetheevidencelinkinganthropometricindicesatdifferentagesandBCrisk,inorder toimproveourunderstandingoftheroleofbodyfatdistributionintheriskofBC,investigatedifferencesintheseassociations accordingtomenopausalstatusandethnicgroups,anddiscussthepotentialbiologicalmechanismslinkingbodysizeandBCrisk. 1.Introduction eincidenceratesofBCshowaheterogeneousdistribu- tion,whileWesterncountriespresentthehighestincidence Breastcancer(BC)isthemostfrequentlydiagnosedcancerin rates, the lowest incidences are observed in low resource womenworldwide,accountingfor23 (1.38million)ofthe countries. BC ranks as the ��h cause of death from cancer totalnewcancercasesin2008[1,2].emajorityofinvasive overall(458,000deaths),butisstillthemostfrequentcauseof breast neoplasms are categorized as%“invasive ductal cell cancerdeathinwomeninbothdeveloping(269,000deaths) carcinoma,nototherwisespeci�ed”(ICD-O8500/3)[3].is and developed regions (189,500 deaths) [1]. Incidence and entityhaslongbeenrecognizedtoincludetumorswithhet- mortality rates have increased in low-incidence countries, erogeneous molecular characteristics, characterized by dis- particularlyinLatinAmerica(LA)andAfricaandespecially tinctpatternsofgeneexpression[4]andofgenomic/genetic amongyoungerwomen.DatafromLAshowthatthehighest alterations[5].SubgroupsofBCarefrequentlydistinguished BC incident rates are among women aged 30–49. In this intoluminal A (estrogen/progesterone-positive),luminal B, area,BCisthemostcommoncanceramongwomen,andthe HER2+,andso-called“triplenegative”subtypes[6].Among leadingcauseofcancermortalitycompoundedbyproblems these subtypes, HER2+ and basal-like subtypes tend to be of access to screening, diagnosis, and treatment [8, 9]. In more common among premenopausal women, as well as Mexicoforexample,BCdeathhasincreased3.6foldbetween in women of African ancestry. Luminal subtypes are more 1995 and 2005. In Africa, a recent study among Gambian commoninpostmenopausalwomenandamongCaucasians women showed an increase of 6.5 in the incidence rate [7]. of BC from 1990 to 2006 [10] compared to 1.5 annually % % 2 JournalofOncology increaseworldwide[11].Asiancountriesarealsorecording indicesatdifferentagesandBCriskinordertoimproveour signi�cant annual increases, for example 2 in Japan and understandingoftheroleofbodyfatdistributionintheriskof 3–5 inChina[11]. BC,toinvestigatedifferencesintheseassociationsaccording e risk factors related to reproductive%factors such as tomenopausalstatusandethnicgroups,andtohighlightthe dela%yedchildbearing,lowerparity,andreducedbreastfeeding potential biological mechanisms linking body size and BC arebecomingmoreprevalentincountriesineconomictran- risk. sitionbutdonotfullyexplaintheincreaseofBCincidence rates.Otherriskfactorssuchaschangesinlifestyle,physical 2.Methods activity,andanthropometryaswellasethnicityandgenetic susceptibility play a role in the development of BC [12– To review the epidemiologic literature on the association 16]. In particular, overweight and obesity have been clearly of overweight, obesity, fat distribution, and BC risk, we associatedwithanincreasedoverallriskofBC. conducted a MEDLINE and PUBMED search including all Overweightandobesityhavebecomemajorpublichealth publications using height, weight, BMI, WC, HC, WHR, challenges throughout the world in both high and low anthropometricfactors,bodyshape,earlylifebodysize,BC, income countries, with over 1 billion overweight and 315 premenopausal,premenopausalBC,case-control,andcohort million obese adults currently estimated worldwide [17, studiesaskeywords.Ourpaperfollowsthepreferredreport- 18]. In the United States (US) for example, obesity is now ingitemsforsystematicreviewsandmeta-analysis(PRISMA) consideredasthesecondleadingcauseofpreventabledeath statementguidelinesdescribedbyLiberatietal.[52].Wethen aer tobacco consumption. Over two-thirds of the adult examinedthereferencesfromtheidenti�edarticles,previous population is overweight, with approximately one-third of review and meta-analysis between anthropometric factors adults and almost 17 of children and adolescents obese andpremenopausalandpostmenopausalBC.eliterature [17,18].Moststudiesontheassociationbetweenobesityand searchincludedallpublicationsfrom1997to2011andrecent BCriskhavebeencond%uctedonCaucasianpopulationsfrom publicationsuptoFebruary2012. Europe,Canada,andtheUS.However,alimitednumberof studiesinotherethnicgroupssuggestsomedifferencesinthe �.�e���t�o��Me�s��e�e�t���d���eo���es�t� prevalenceofobesityandfatdistributionamongwomen.For example studies in the US show that American women of Overweightandobesityarede�nedasabnormalorexcessive AfricanorHispanicoriginaremorelikelytobeobesethan fat accumulation that may impair health [61]. ere are Caucasian women [19]. Given the disparities in prevalence differentwaystomeasureobesity;BMIisthemostcommonly rates of obesity, it is expected that among women, 69 of usedandiscalculatedasweight(kg)dividedbyheight(m ). Caucasians,87 ofAfricanAmericans,and80 ofHispanics eWorldHealthOrganization(WHO)classi�esthedegree willbeoverweightin2015[19]. % 2 of adiposity in terms of the BMI as follows: underweight, Anthropom%etricindices,height,weight,bo%dymassindex less than 18.5; normal, 18.5–24.9; overweight, 25.0–29.9; (BMI),waistcircumference(WC),hipcircumference(HC), obese, more than 30.0kg/m (Table 1(a)). While BMI is or waist-to-hip ratio (WHR), are commonly used as tools usuallyassociatedwithgeneralobesity,WCandWHRhave for assessing overweight/obesity and recently methods for 2 beenusedasmeasuresofcentralorintra-abdominalobesity, evaluating body shape and body size at different ages have de�ned as waist–hip ratio above 0.90 for males and above also been used. Several studies and meta-analyses have 0.85 for females (Table 1(b)). However, there is evidence of examined the associations between anthropometric indices important ethnic variations in body fat distribution, espe- and BC among both pre- and postmenopausal women. ciallyinAsiansascomparedtoCaucasians.InAsianadults, Overall consistent positive associations have been observed differences in body build and body composition result in a between BMI and WHR and the risk of BC among post- differentrelationshipbetweenBMIandbodyfatdistribution menopausalwomen[20–29],whilecon�ictingresultspersist relativetoCaucasians[62–64].InastudyofyoungJapanese forpremenopausalBC,bothforBMIandforotheranthro- and Australian men, Kagawa and colleagues reported that pometric parameters [29–36]. Possible differences in these Japanesemenwereestimatedtohaveanequivalentamount associationscouldberelatedtodifferentialrolesoffatandfat of body fat as the Australian men at BMI values about 1.5 distributiononmetabolismandtotheircontributiontoBC development among pre- and postmenopausal women [31, units lower than those of the Australians (23.5kg/m and 32]. Waist circumference (WC) and WHR, which correlate 28.2kg/m , resp.) [65]. Similarly, studies among Ch2inese with central (abdominal) obesity have been associated with reported s2imilar relationship between BMI and body fat increased BC risk in postmenopausal women [32, 37–39], distribution [43]. ese observations suggest that Asian but not in premenopausal women for whom both null peoplearemorelikelytohavehigherlevelsofbodyfatoverall [23, 38, 39] and increased risk have been reported [31, 32, andmoreabdominalfatandlowerleanmassthantheother 37, 40]. Furthermore, the relation between premenopausal ethnic groups for a given BMI [41–43]. Consequently, the BC and anthropometry has shown inconsistencies across level of BMI that the WHO recommends for overweight ethnic groups [41–43]. ese inconsistencies may be due and obesity in Caucasians may not be applicable for Asian to important ethnic variations in body fat distribution. adults.eWHOWesternPaci�cRegionalO�ce(WPRO) We conducted a systematic review of published studies to has proposed a de�nition of obesity in Asian populations evaluatethestrengthofassociationsbetweenanthropometric withoverweightde�nedasBMI23.0–24.9kg/m andobesity 2 JournalofOncology 3 T1:(a)Combinedrecommendationsofbodymassindexandwaistcircumferencecut-offpointsmadeforoverweightorobesity,and associationwithdiseaserisk.(b)WorldHealthOrganisationcut-offpointsandriskofmetaboliccomplications. (a) Bodymassindex Obesityclass Diseaserisk(relativetonormalweightandwaistcircumference) Men 102cm Men 102cm Women 88cm Women 88cm < > Underweight 18.5 < > Normal 18.5–24.9 < Overweight 25.0–29.9 Increased High 30.0–34.9 I High Veryhigh Obesity 35.0–39.9 II Veryhigh Veryhigh Extremeobesity 40 III Extremelyhigh Extremelyhigh (b) > Indicator Cut-offpoints Riskofmetaboliccomplications Waistcircumference Men 94cm;women 80cm Increased Waistcircumference Men 102cm;women 88cm Substantiallyincreased Waist-hipratio Men >0.90cm;women>0.85cm Substantiallyincreased > > ≥ ≥ Author, year Ethnicity/race RR 95% CI Cohort studies Lahman et al., 2004 [23] Caucasian 1.31 1.08–1.59 Tehard and Clavel-Chapelon, 2006 [28] Caucasian 1.44 1.04–1.99 Palmer et al., 2006 [35] African-American 0.78 0.58–1.05 Kuriyama et al., 2005 [46] Asian 2.67 1.03–6.92 Iwasaki et al., 2007 [47] Asian 2.28 0.94–5.52 Kawai et al., 2010 [22] Asian 2.54 1.16–5.55 Case-control studies Friedenreich et al., 2002 [48] Caucasian 0.99 0.74–1.32 Hall et al., 2000 [40] Caucasian 1.08 0.58–2.01 Berstad et al., 2010 [30] Caucasian 0.75 0.53–1.06 Wenten et al., 2002 [50] Caucasian 2.77 0.86–8.91 Slattery et al., 2007 [36] Caucasian 1.61 1.05–2.46 Hall et al., 2000 [40] African-American 0.68 0.33–1.41 Berstad et al., 2010 [30] African-American 1.26 0.69–2.31 Ogundiran et al., 2010 [34] African 0.76 0.48–1.21 Adebamowo et al., 2003 [49] African 1.82 0.77–4.28 Chow et al., 2005 [20] Asian 1.73 1.04–2.87 Wu et al., 2007 [39] Asian 1.35 0.95–1.93 Mathew et al., 2008 [24] Asian 1.29 1.00–1.67 Wenten et al., 2002 [50] Hispanic 1.32 0.47–3.72 Slattery et al., 2007 [36] Hispanic 0.80 0.44–1.45 Meta-analysis studies Van Den Brandt et al., 2000 [29] Caucasian 1.26 1.08–1.47 Suzuki et al., 2009 [27] All 1.33 1.19–1.48 Renehan et al., 2008 [25] All 1.12 1.05–1.19 0 2 4 6 8 RR F1:ForestplotoftheassociationbetweenBMIandbreastcancerriskinpostmenopausalwomen.esizeofeachboxindicatesthe relativeweightofeachstudy;thehorizontalbarsshowthe95 con�denceintervals(CI).RR:relativerisk;95 CI:95 con�denceintervals. % % % 4 JournalofOncology Variablesofadjustmentorcomment Studycenter,age,educationalattainment,smokingstatus,alcoholconsumption,parity,ageat�rstpregnancy,ageatmenarche,andcurrentpilluse FHBC,ageatmenarche,ageat�rstbirth,parity,historyofbenignbreastdisease,alcoholconsumption,numberofyearsofeducation,maritalstatus,andphysicalactivity Age,educationstatus,ageatmenopause,ageatmenarche,parity,ageat�rstbirth,BMIatage18years,OC,HRT,smoking,alcohol,andphysicalactivitylevel Age,timeperiod,parity/ageat�rstbirth,FHBC,personalhistoryofbenignBC,height,alcoholintake,OCuse,birthweight,ageatmenopause,andHRTuse Age,smoking,alcohol,consumptionofmeat,�sh,fruits,greenoryellowconsumptionofbean-pastesoup,typeofhealth,parity,ageatmenarche,andageatFFTpregnancy Age,area,numberofbirths,ageat�rstbirth,andheight Age,education,smoking,alcohol,andtimespentwalking,Menstrualandreproductivefactors,HRT,andFHBC Age,ageatmenarche,parity,ageat�rstbirth,andfamilyhistoryofbreastcancer Age,totalcaloricintake,physicalactivity,educationallevel,HRT,diagnosedwithbenignBC,FHBC,alcohol,andcurrentsmoke dedinthepaper. RR(95CI) %1.31(1.08–1.59)0.66(0.45–0.98) 0.94(0.74–1.21)0.85(0.60–1.20) 1.44(1.04–1.99)1.03(0.83–1.28) 0.85(0.74–0.98) 0.93(0.90–0.95)0.91(0.89–0.93) 2.67(1.03–6.92) 2.28(0.94–5.53) 2.54(1.16–5.55) 0.55(0.37–0.82)0.78(0.58–1.05)1.01(0.74–1.40) 0.99(0.74–1.32)1.43(1.07–1.93) u cl n i n e menopausalwome Rangeofexposure 30versus2530versus25><><0.84versus0.730.84versus0.73><><30versus18.50.82versus0.74 ≥<≥ boveversusaverag 0.1unitincrease0.1unitincrease 30versus25 ≥< 30versus19 ><25versus20 25versus20≥<37versus250.87versus0.71≥<≥<31.3versus24.1≥<0.83versus0.75 ≥<≥< st A o p n i Y dies 10Y–20 stu ure 12 5–10 racteristicsof Typeofexpos BMInon-HRTHRTWHRnon-HRTHRT BMIWHR Weightatage BodyfatnessChildhoodAdolescent BMI BMI BMI BMIatage18CurrentBMIWHR BMIWHR a h c 2:Selected Cases/controlsorP-years 1,405/103,344 860/41497 2503/35941 4974/188,860 65/9,666 441/55,537 108/10,106 455/59,000 771/762  T Population Caucasian Caucasian Caucasian Caucasian Asian Asian Asian African-American Caucasian n ol udydesig ohort ohort ohort ohort ohort ohort ohort ohort ase-contr St C C C C C C C C C r, 4] 5] 5] Firstauthor,yeaandcountry Lahmann2004Germany[23] Tehard2006France[28] Bardia2008UnitedStates[4 Baer2010UnitedStates[4 Kuriyama2005Japan[46] Iwasaki2007Japan[47] Kawai2010Japan[22] Palmer2007UnitedStates[3 Friedenreich2002Canada[48] JournalofOncology 5 Variablesofadjustmentorcomment Ageatmenarche,nulliparity,breastfeeding,Abortionormiscarriage,BMI,WHR,oralcontraceptive,HRT,FHBC,smoking,alcohol,education,medicalradiationtothechest Age,ageatmenarche,parity/ageatFFTpregnancy,lactation,andeducation Age,race,education,studysite,FHBC,parity,ageatmenopause,andHRT Age,ethnicity,education,menarche,parity,ageatFFTP,breastfeeding,menopausalstatus,ageatmenopause,FHBC,benignbreastdisease,contraceptive,alcohol Age,ageatmenarche,ageatFFTpregnancy,height Age;FHBC;totalMET-hours;parity;OC;breastfeeding;ageat�rstlivebirth; monthsofHRTuse Age,center,physicalactivitylevel,energyintake,alcoholintake,ageatmenopause,parity,andHeight Age,menopausalstatus,ageatmenarche,parity,numberofbirth,ageatFFTbirth,HRT,OC,breastfeeding,smoking,height,weight,andBMI Age,numberofpregnancies,familyhistoryofbreastcancer,income,smoking,alcohol,useofOC,andeducation RR(95CI) % 1.40(1.10–1.70) 0.68(0.33–1.42)1.08(0.58–2.00) 1.62(0.70–3.79)1.64(0.88–3.07) 0.72(0.55–0.96) 0.75(0.53–1.06)1.26(0.55–1.85) 0.76(0.48–1.21) 1.82(0.78–4.31) 2.77(0.86–8.89)1.32(0.47–3.72) 1.61(1.05–2.45)0.80(0.44–1.45) 1.51(0.93–2.46)0.77(0.39–1.50) 8.19(3.40–19.50) 1.73(1.04–2.86)3.82(1.03–14.27) 4.64.6 7777 Continued. Rangeofexposure 0.8versus0.8 >≤ 30.1–59.2versus14.6–230.1–59.2versus14.6–2 0.86–1.34versus0.6–0.0.86–1.34versus0.6–0. 25versus20 ≥<35versus2535versus25≥<≥< 28versus21 ≥< 30versus20 ≥<30versus2230versus22≥<≥<30versus2530versus25><><0.9versus0.80.9versus0.8><><0.86versus0.75 >< 23–27versus1931versus19 <<< 2:  n r T ure rs merica Tuser RTuse peofexpos HR MIBlackWhiteHRBlackWhite MIat18yeacentBMICaucasianAfrican-A MI MI MICaucasianHispanic MInon-HR CaucasianHispanicHRnon-HCaucasianHispanic HR MI y W W e W W T B BR B B B B B s ol ntrs 06 25 Cases/coorP-year 436/354 382/419 1,900/2,0 498/266 234/273 687/820 2,325/2,5 130/585 198/353 Population CaucasianAfrican-American CaucasianAfrican-American CaucasianAfrican-American African African CaucasianHispanic CaucasianHispanic Asian Asian n ol ol ol ol ol ol ol ol ol desig contr contr contr contr contr contr contr contr contr y - - - - - - - - - d e e e e e e e e e u as as as as as as as as as St C C C C C C C C C Firstauthor,year,andcountry Huang1999UnitedStates[38] Hall2000UnitedStates[40] Berstad2010UnitedStates[30] Ogundiran2010Nigeria[34] Adebamowo2003Nigeria[49] Wenten2002UnitedStates[50] Slattery2007UnitedStates[36] Ng1997Singapore[33] Chow2005China[20] 6 JournalofOncology Variablesofadjustmentorcomment Age,Asianethnicity,durationofresidenceintheUS,education,menarche,parity,menopausalstatus,ageatmenopause,intakeofteaandsoy,andphysicalactivity Age,center,religion,maritalstatus,educationsocioeconomicstatus,residencestatus,parity,ageat1stchildbirth,durationofbreastfeeding,andphysicalactivity Ameta-analysiswasdonetosummarizetheliteratureonWHRandbreastcancerriskpublishedfromJanuary1966toAugust2002 Lifestylesandreproductivefactors(confoundersthatwerefoundtobesigni�cantinproportionalhazardregressionanalysis)Meta-analysisofcohortandcase-controlstudies(from1970to2007)wasperformedtoclarifytheassociationbetweenbodyweightandtheincidenceofBCde�nedbyER/PRstatusofthetumors HRT,OC,historyofbenignbreastdisease,FHBC,smokingstatus,education,fatintake,�berintake,energyintake,andalcoholintake Cohortandcase-controlstudiespublishedfrom1966toNovember2007wereincludedintheanalysis.edoseresponsemeta-analysiswasadjustedbygeographicregionandcancersite Age,ethnicity,comorbidity,andmenopausalstatus placementtherapy;OC:oralcontraceptives;FFT: e r RR(95CI) %1.35(0.95–1.93)1.48(1.02–2.15) 1.29(1.00–1.66)1.00(0.64–1.54) 1.50(1.10–2.04) 1.32(1.16–1.49) 1.82(0.85–3.85) 1.33(120–1.48) 1.26(1.09–1.46) 1.12(1.08–1.16)1.15(1.08–1.23)1.09(1.04–1.48)1.31(1.15–1.48) 4.8(1.8–12.7)1.4(0.5–4.1) cer;HRT:hormonal n a c ast Continued. Rangeofexposure 24.60versus20.430.84versus0.76 >≤>≤ 25–29.9versus2530versus25 <>< 0.1unitincrease 0.75versus0.80 0.75versus0.80 0.5unitincrease 21versus31 5unitsincrease5unitsincrease5unitsincrease5unitsincrease 30versus2530versus25≥<gesteronereceptor;BC:bre≥< o 2: pr T Typeofexposure BMIWHR BMI WHR WHRCohortstudiesCase-controlstudies BMIER+PR+ BMI BMIallNorthAmericanEuropeanandAustralianAsia-Paci�c BMIAfrican-AmericanHispanic R:estrogenreceptor;PR:ars. Ee Cases/controlsorP-years 1,277/1,160 968/691 19studies 8studies:5cohortand3case-control 31studies:9cohortand22case-control 4,385/337,819 31studies 237/234 R:waist-hipratio;breastcancer;�:y Hof Wy Population Asian Asian All All All Caucasian CaucasianAsian African-AmericanHispanic 2(inkg/m);familyhistor Firstauthor,year,Studydesignandcountry Wu2007Case-controlJapan[39] Mathew2008Case-controlIndia[24] Connolly2002Meta-analysisCanada[37] Harvie2003Meta-analysisUnitedkingdom[32] Suzuki2009Meta-analysisSweden[27] VanDenBrandt2000Meta-analysisUnitedStates[29] Renehan2008UnitedStatesMeta-analysis[25] Sarkissyan2011Cross-UnitedStates[51]sectional BMI:measurementofbodymassindexageat�rstfull-termpregnancy;FHBC:Bold:statisticallysigni�cant. JournalofOncology 7 de�nedasBMI 25kg/m .Inaddition,WHOhassuggested due to the small number of cases, in particular in post- that a waist circumference of 90cm for men and 80cm for menopausal women, re�ecting the demographic structure 2 women was use≥d as interim lower values for Asians as the of African populations. Another possible explanation for cut-off point to de�ne overweight instead of 94cm in men these differences may be the selection bias mainly in case- and85cmforCaucasianwomen[66]. control studies, where anthropometric measurements are oen obtained aer diagnosis and may be affected by the effectsofcancerdevelopmentonthegeneralconditionofthe 4.InPostmenopausalWomen patient. e lack of association between BMI and BC risk observedinHispanicwomenmayre�ectdifferenteffectsof 4.1.BMIandBreastCancerRisk. Mostavailablestudiesand fataccumulationanddistributioninthisHispanicpopulation meta-analyses have focused on BMI as a marker of general comparedtopopulationsinhighresourcecountries. obesity [22, 24, 25, 27–29, 67] and indicated an overall increase in the risk of postmenopausal BC in overweight or obese women among all ethnic groups (Table 2). Figure 4.2.WHRandBreastCancerRisk. WHRiscommonlyused 1 summarizes studies of the association between BMI and as a measure of central obesity [31, 32, 70], de�ned as breast cancer risk in postmenopausal women. A meta- waist-hip ratio above 0.90 for males and above 0.85 for analysis of some of these studies conducted by Renehan femaleshasoenbeenassociatedwiththeriskofdeveloping observed an overall 12 increase per 5kg/m increase in postmenopausalBC(Table2).However,whilemoststudies BMI (RR ; CI: 1.08–1.16) [25]. However estimates have reported a signi�cant increased risk [33, 37–39, 48], 2 may vary according to%geographic regions; the association somestudiesareinconclusive[23,35,40](Figure2).Ameta- tended to b=e s1t.r1o2nger in studies from Asia Paci�c (RR analysiswithsixcase-controland�vecohortstudiesobserved ;95 CI:1.15–1.48)thanstudiesfromNorthAmerica, a summary risk estimate of 1.50 (95 CI: 1.10–2.04) for Europe, and Australia (RR = 1.15; 95 CI: 1.08–1.23 an=d postmenopausal women [37]. e associations tend to be 11..3019;95%CI:1.00–1.14,resp.).Pooleddatafromsevencohort strongerinAsianwomenthanotheret%hnicgroups[33].Ina studies including 337,819 women and%4,385 incident BC Canadiancase-controlstudy,apositiveincreaseinRRof1.43 casesfo%unda26 increaseinpostmenopausalBCriskwith (95 CI:1.07–1.93)wasobservedwhencomparingthehigh- BMIsgreaterorequalto28kg/m [29].Inmostcase-control est ( 0.83) to the lowest quintile ( 0.75) [48]. Similarly, in and prospective%studies, a positi2ve and strong relationship the%Carolinacase-controlstudy,theORforpostmenopausal hasbeenobservedbetweenBMIandpostmenopausalAsian wom>en in the highest quintile ( 0<.8) compared to lowest women [20, 22, 67]. In a cohort study of 10,106 women, quintile ( 0.8) was 1.40 (95 CI: 1.1–1.7) [38]. A study in conductedinJapan,theRRfordevelopingpostmenopausal Africa(Nigeria)reportedanRRof>2.67;95CI(1.05–6.80)for BC was 2.54; 94 CI (1.16–5.55) in women with BMI of postmeno≤pausalwomenwith%WHR 0.85comparedtothose 25kg/m or above compared to those with less 20.5kg/m withWHR 0.77[71].Incontrast,somestudiesconducted [22]. In2contrast%, there is a lack of data among women2 intheUSdidnotdetectasigni�can>tassociation.Halletal. of African origin, but the notion that increase in BMI reportedan<onincreasedRRof1.62;95 CI(0.70–3.79)in is associated with the risk of postmenopausal BC in this AfricanAmericanwomenandof1.64;95 CI(0.88,3.07)for population is consistent with a recent case-control study CaucasianAmericanwomenwhencomp%aringhighestversus reporting a positive association between high BMI and an lowest quintiles (0.86–1.34 versus 0.6–0%.77) [40]. However increasedriskofestrogenreceptorandprogesteronereceptor the power of the study was limited by the small number positiveBC(OR=1.83;95 CI:1.08–3.09;P trend=0.03) of cases (179 cases and 182 controls in African women). RegardingHispanicwomen,onlyonestudyhasassessedthe comparingthehighest( 35kg/m )tothelowest( 25kg/m ) associationbetweenWHRandBCrisk.isstudyfoundno quintile[30].Otherstudies%onwo2menofAfricandescentd2o signi�cant association between WHR and postmenopausal not support a positive>association between BMI<and post- BCrisk[36](Figure2). menopausalBC[34,35,40,49].Inaprospectivestudyamong AfricanAmericans,Palmeretal.reportedanonstatistically signi�cantdecreasingtrendforwomenwithBMIof35kg/m 5.InPremenopausalWomen or above compared to 25kg/m [35]. Similarly, a recen2t case-control study including 505 postmenopausal BC cases 5.1.BMIandBreastCancerRisk. Previousstudies,reviews, 2 and 278 controls found<a RR of 0.76; CI (0.48–1.21) for and pooled analyses have addressed the association of BMI womenwithBMI 28kg/m comparedto 21kg/m [34]. and premenopausal BC (Table 3). Figure 3 summarizes FewstudiesontheassociationbetweenobesityandBChave studies of the association between BMI and breast cancer 2 2 been conducted in≥Hispanics, of those, mos<t have reported risk in premenopausal women. In 2000, Van den Brandt et inconsistent association between BMI and risk of BC in al.analyzedtheassociationbetweenpremenopausalBCand postmenopausalwomen[50,68,69].Recently,Sarkissyanet BMIusingpooleddatafromsevenprospectivecohortstudies al.(2011)reportedinacross-sectionalstudy,alackofassoci- in Caucasian women. Multivariate analyses controlling for ationbetweenobesitymeasuredbyBMIandpostmenopausal reproductive, dietary, and other risk factors detected that BC among Hispanic women in the US population (OR = when compared to premenopausal women with a BMI of 1.4, 95 CI: 0.5, 4.1) [51]. e heterogeneity among these lessthan21kg/m ,womenwithaBMIexceeding31kg/m �ndingsmaybeduetothelackofpowerinAfricanstudies hadanRRof0.54(95 CI:0.34–0.85),suggestinganinverse 2 2 % % 8 JournalofOncology Author, year Ethnicity/race RR 95% CI Cohort studies Lahman et al., 2004 [23] Caucasian 0.94 0.73–1.20 Tehard and Clavel-Chapelon, 2006 [28] Caucasian 1.03 0.83–1.28 Palmer et al., 2006 [35] African-American 1.01 0.74–1.39 Case-control studies Friedenreich et al., 2002 [48] Caucasian 1.43 1.06–1.93 Huang et al., 1999 [38] Caucasian 1.40 1.13–1.73 Slattery et al., 2007 [36] Caucasian 1.51 0.93–2.46 Hall et al., 2000 [40] Caucasian 1.64 0.88–3.07 Hall et al., 2000 [40] African-American 1.62 0.70–3.77 Adebamawo et al., 2003 [71] African-American 2.67 1.05–6.79 Slattery et al., 2007 [36] Caucasian 1.51 0.93–2.46 Ng EH et al., 1997 [33] Asian 8.19 3.42–19.64 Wu et al., 2007 [39] Asian 1.48 1.02–2.15 Slattery et al., 2007 [36] Hispanic 0.77 0.39–1.51 Meta-analysis studies Connolly et al., 2002 [37] All 1.32 1.17–1.49 Harvie et al., 2003 [32] All 1.33 1.19–1.48 0 1 2 3 4 5 6 7 RR F2:ForestplotoftheassociationbetweenWHRandbreastcancerriskinpostmenopausalwomen.esizeofeachboxindicatesthe relativeweightofeachstudy;thehorizontalbarsshowthe95 con�denceintervals(CI).RR:relativerisk;95 CI:95 con�denceintervals. % % % associationbetweenBMIandriskofpremenopausalBC[29]. casesand1,182controlsreportedanincreasedriskof33–56 Adose-responsemeta-analysisonBMIandpremenopausal when comparing premenopausal women above 25kg/m BC was conducted by Renehan et al. using a dataset of 20 with those with than less 25kg/m (OR = 1.33; 95 C%I2: studies. is analysis detected an overall risk estimate of 1.50–1.62forBMI25–29.9kg/m and21.56;95 CI:1.03,2.35 0.92(95 CI:0.88–0.97)foreachincrementof5kg/m [25]. forBMIgreaterthan30kg/m )[224].Interestinglyoner%ecent Several studies supported the hypothesis that higher level 2 cohort study conducted in Japan reported a%high increased of BMI%may be associated with a decrease in the risk of 2 risk of 2.54; 95 CI (1.16–5.55) when comparing women premenopausal BC. is hypothesis is supported by results of BMI 25kg/m to those of 20kg/m [22]. In contrast, fromseveralcase-controlstudies[34,39,40,60]andcohort otherstudiesam%ongAsianwomendidnotdetectasigni�cant studies [35, 53]. However, others studies did not observe a 2 2 statistically signi�cant association when comparing highest associationbetweenBMIandth<eriskofpremenopausalBC [20, 47]. Among African women, the majority of studies versus lowest levels of BMI [23, 49, 56]. Ethnicity appears to modify the association of overweight, obesity, and BC. reported an inverse association between obesity and pre- While the inverse association between BMI and risk of menopausalBC.Acase-controlstudyconductedinNigeria premenopausal BC is well documented in Caucasians, the reportedasigni�cantdecreasingtrendinpremenopausalBC association among Asian women is inconsistent. Several withincreasingBMI(Ptrend=0.027)[34].Asimilar�nding studies among Asian women suggest that higher BMI may wasobservedinalargeprospectivestudyconductedamong be associated with an increased risk for premenopausal BC African Americans in whom the multivariate adjusted RR [22,24,46,55].Aprospectivestudyincluding11,889women was 0.72 (95 CI: 0.54–0.96) for BMI 25kg/m relative from Taiwan reported that higher BMI was moderately to BMI 20 [35]. In contrast, some studies did not �nd a 2 associatedwithanincreasedriskofpremenopausalBC[55], signi�cant as%sociation [30, 40]. With re>spect to Hispanics, with an OR of 1.90 (1.00–3.4) for BMI 26.2kg/m versus a case-co<ntrol study conducted on Hispanic women living 21.6kg/m .Similarlyamulti-centriccase-controlstu2dycon- in the US concluded that high BMI at 30 years of age was ducted am2ong urban and rural women>and including 898 associated with a decrease of the risk of premenopausal JournalofOncology 9 BC (OR = 0.46, 95 CI: 0.25, 0.84 for BMI 30 versus 7.VariationswithMolecularSubtypesof 25kg/m ) [36]. A more recent study has shown that high BreastCancer BMI was2inversely a%ssociated with risk of BC>in Hispanic <population(Ptrend 0.01)[58]. e association between obesity and BC appears to vary according to the molecular subtype of BC, as de�ned by gene expression patterns into luminal A and B, HER2+, < 5.2.WHRandBreastCancerRisk. WHRhasnotbeencon- and triple-negative subtypes. A meta-analysis suggests that sistentlyassociatedwithincreasedBCriskinpremenopausal the association between BMI and BC risk is heterogeneous women, for whom both null [23, 38, 39] and increased accordingtoestrogenreceptor(ER)andprogesteronerecep- risk have been reported [31, 32, 37, 40] (Figure 4, Table tor (PR) status of the tumor. Higher BMI was associated 3). Two meta-analyses [32, 37] have reported that a greater with higher risk for ER+/PR+ tumors in postmenopausal WHR was associated with about 1.5 fold increased risk women(RR=1.82;95 CI:1.55–2.14)buthadaprotective of premenopausal BC. A pooled analysis on seven cohorts effectonER+/PR+tumorsinpremenopausalwomen(RR= and four case-controls reported a summary risk estimate 0.80; 95 CI: 0.70–0.9%2). By contrast, no associations were of 1.79; 95 CI (1.22–2.62) [37] but the strength of the observed for ER PR tumors [27]. In 2011, Harris et al. association varied according to ethnic groups [41–43, 64]. investiga%ted the association between body fat distribution, A large pro%spective cohort study of 11,889 women con- assessedin1993b−ysel−f-reportedWC,HC,andWHR,andthe ducted in Taiwan found that central adiposity re�ected by incidenceofpremenopausalBCintheNurses’HealthStudy hip circumference was a signi�cant predictor of BC [55]. II.Eachofthesebodyfatdistributionmeasuresappearedto Similarly,inaprospectivecase-controlstudyinvolving1,086 bestatisticallysigni�cantlyassociatedwithgreaterincidence Chinese women in Singapore, central obesity as indicated of estrogen receptor (ER) negative BC (RR for ER-negative by a larger WHR was associated with highest risk for BC, BC for the highest versus the lowest quintile of WHR was with the OR being 7.81; (95 CI: 2.8–21.9) comparing the 1.95(95 CI:1.10–3.46;Ptrend=0.01)[31].ese�ndings last ( 0.86) and �rst quintile ( 0.75), whereas BMI did not suggest that body fat distribution may be associated with signi�cantlypredicttherisk%forBC[33].AmongCaucasian anincre%asedriskforER-negativeBCamongpremenopausal wome>n, a case-control study i<ncluding 523 cases and 471 women. controls,adjustedforBMI,reportedanincreaseriskof1.04 Inapooledanalysisoftumormarkerandepidemiological (1.01–1.08)foreachincrementof0.1unitofWHRandarisk riskfactordatafrom35,568invasiveBCcasepatientsfrom of2.44;95 CI(1.17–5.09)whencomparingthe(0.86–1.34) 34studiesparticipatingintheBCAssociationConsortium, versus(0.6–0.77)quintiles[40].Fewstudieshavebeencon- obesity (BMI 30kg/m ) in women 50 years was found ductedon%Africanwomen(AfricanAmericanandAfrican); to be more frequent in ER /PR than in ER+/PR+ tumors amongthose,acase-controlstudyconductedamongAfrican 2 ( ).In≥contrast,obesityinwom≤en 50yearswasless American found a positive association between WHR and premenopausalBC(RR=2.50;95 CI:1.1,5.67,Ptrend frequenti−n7PR thaninPR−+tum−ors( )[75].is 0.005)forwomenwithWHR(0.86–1.34)comparedtothose s𝑃𝑃tud𝑃y𝑃d𝑃𝑃e𝑃monstrated that elevated BMI in>you−n4ger women withWHR(0.6–0.77)[40].Others%tudies[55,58,72]didno<t ( 50years)wa−sassociatedwiththeris𝑃𝑃k𝑃of𝑃E𝑃𝑃R𝑃+orPR+BC �ndastaticallysigni�cantassociation.Overall,thisincreased butnotwithER /PR BCandsuggestedthattriple-negative risk associated with larger WHR among premenopausal o≤rcorebasalphenotype(CBP);de�nedbytriple-negativeand women is found to be stronger amongst Asian women cytokeratins[CK−s]5/−6+(CBP)BCmayhavedistinctetiology comparedtootherethnicgroups.Studiesconductedbetween [75]. e differences between the conclusions of the two WHR and premenopausal BC among Hispanic women are studies[31]maybelinkedtotheuseofdifferentobesity/fat limited and none has reported signi�cant association. For distribution measures. Further studies are needed to better example,Johnetal.,reportedanonsigni�cantdecreaserisk understandtheassociationsbetweenoverweightandobesity ofhavinggreaterWHRamongHispanicwomen(OR=0.71, andspeci�csubtypesofBC. 95 CI:0.46–1.1;Ptrend=0.19)[58]. 8.EffectofEarlyLifeAnthropometryon % �.Si�ni�canceof�aist�to��ei�htRatio BreastCancerRisk ere is evidence suggesting that the waist-to-height ratio Mostoftheepidemiologicalstudieshavefocusedmainlyon (WHtR)maybeamoreusefulglobalclinicalscreeningtool adult BMI and not on weight change or on the in�uence thanWC,withaweightedmeanboundaryvalueof0.5[73]. ofearlylifebodyweightandbodyshape(silhouette).ese e WHtR is de�ned as waist (cm) circumference divided factors, such as birth size, body shape, and weight during by height (cm) and correlates well with abdominal obesity; childhoodoradolescencemayplayaroleintheriskofBC. highervaluesofWHtRindicatehigherriskofobesity-related Epidemiologicstudieshavedemonstratedthatindependently cardiovasculardiseases[74].However,todatetheassociation ofBMI,greaterbodyfatnessduringchildhoodoradolescence between WHtR and BC risk has not been systematically are associated with lower BC risk in both premenopausal studied.Nevertheless,apreviousstudyofmultiethnicgroups women[30,36,45,53,54,57]andpostmenopausalwomen reportedaninverseassociationbetweenWHtRandER+PR+ [30, 35, 44, 45]. In a recent large prospective study con- BCinallpremenopausalwomen[58]. ductedamong188,860women,Baerandcolleaguesreported 10 JournalofOncology Variablesofadjustmentorcomments Ageatenrolment,parity,ageatFFTpregnancy,OC,ageatmenarche,FHBC,totaldurationofbreastfeeding,andcountry Studycenter,age,educationalattainment,smoking,alcohol,parity,ageat�rstpregnancy,ageatmenarche,andcurrentpilluse Age,timeperiod,birthweight,height,recentalcoholconsumption,parity,ageat�rstbirth,OC,historyofbenignbreastdisease,and�rstdegreeofFHBC FHBC,ageatmenarche,ageatFFTP,parity,historyofbenignbreastdisease,alcoholconsumption,education,maritalstatus,andphysicalactivity Age,timeperiod,parity,ageat�rstbirth,FHBC,personalhistoryofbenignbreastdisease,height,alcoholintake,OC,andbirthweight Age,height,historyofbenignbreastdisease,FHBC,ageatmenarche,ageatFFTP,parity,OC,alcohol,andphysicalactivity Age,smoking,alcohol,consumptionofmeat,�sh,fruits,greenoryellowconsumptionofbean-pastesoup,typeofhealth,parity,ageatmenarche,andageatFFTpregnancy Age,area,numberofbirths,ageat�rstbirth,andheight Ageatenrollment,height,weight paper. CI) %40–0.97)59–0.91)50–0.93) 59–1.14)74–1.50) 61–0.98)65–0.91) 67–0.99) 06–1.00)39–0.91) 87–0.94) 87–0.94) 10–3.46) 24–2.88)03–6.92) 53–3.47) 00–3.40)30–1.20) e 5 0.0.0. 0.0. 0.0. 0. 0.0. 0. 0. 1. 0.1. 0. 1.0. h 9 ((( (( (( ( (( ( ( ( (( ( (( t ( 249 25 77 2 60 1 8 5 47 7 00 n R 676 80 77 8 26 9 8 9 86 4 96 di R 0.0.0. 0.1. 0.0. 0. 0.0. 0. 0. 1. 0.2. 1. 1.0. nclude erage angeange ange menopausalwomeni Rangeofexposure 30versus2025versus20–24.9Fat/veryfatversusav><≥ 28.8versus21.50.846versus0.736 ≥<>< 2levelsversusnoch2levelsversusnoch≥2levelsversusnoch≥ ≥30versus18.50.82versus0.74 ><≥ 0.2unitincrease 0.1unitincrease 0.84versus0.73 ≥< 29.9versus2530versus25 ≥<≥< 30versus19 26.2versus21.6><0.85versus0.77 ><< e diesinpr ure age7 fatnessto10to20 0to20 5–10Y 10–20Y cteristicsofstu Typeofexpos BMIBMIatage18Bodyshapeat BMIWHR IncreasebodyFromage5Fromage5 Fromage1 BMIWHR BodyfatnessChildhood Adolescent WHRER − BMI BMI BMIWHR a 3:Selectedchar Cases/controlsorP-years 733/99,717 474/73,542 1,318/109,267 275/20,068 2,188/188,860 620/45,799 33/5,214 441/55,537 104/11,889    T opulation aucasian aucasian aucasian aucasian aucasian aucasian sian sian sian P C C C C C C A A A n g si e yd ort ort ort ort ort ort ort ort ort d h h h h h h h h h u o o o o o o o o o St C C C C C C C C C 4 6 Authors,years,andcountry Weiderpassetal.,200Norway-Sweden[53] Lahmannetal.,2004Germany[23] Baeretal.,2005UnitedStates[54] TehardandClavel-Chapelon,200France[28] Baeretal.,2010UnitedStates[45] Harrisetal.,2011UnitedStates[31] Kuriyamaetal.,2005Japan[46] Iwasakietal.,2007Japan[47] Wuetal.,2006Taiwan[55]

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1 Nutritional Epidemiology Group, Nutrition and Metabolism Section, 2 International Prevention Research Institute, 95 Cours Lafayette, 69006 Lyon, France An estimated 1.38 million new cases of breast cancer (BC) are diagnosed each year Other risk factors such as changes in lifestyle, physical.
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