Elevated Serum Pesticide Levels and Risk for Alzheimer Disease

被引:154
|
作者
Richardson, Jason R. [1 ,2 ]
Roy, Ananya [2 ]
Shalat, Stuart L. [1 ,2 ]
von Stein, Richard T. [2 ]
Hossain, Muhammad M. [1 ,2 ]
Buckley, Brian [2 ]
Gearing, Marla [4 ]
Levey, Allan I. [3 ]
German, Dwight C. [5 ]
机构
[1] Rutgers Robert Wood Johnson Med Sch, Dept Environm & Occupat Med, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Environm & Occupat Hlth Sci Inst, Piscataway, NJ USA
[3] Emory Univ, Sch Med, Dept Neurol & Alzheimers Dis, Atlanta, GA USA
[4] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[5] Univ Texas SW Med Ctr Dallas, Dept Psychiat, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
ORGANOCHLORINE PESTICIDES; OCCUPATIONAL-EXPOSURE; PARKINSONS-DISEASE; DDT; COMMUNITY; LIMITS; INDIA; BLOOD;
D O I
10.1001/jamaneurol.2013.6030
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IMPORTANCE The causes of late-onset Alzheimer disease (AD) are not yet understood but likely include a combination of genetic, environmental, and lifestyle factors. Limited epidemiological studies suggest that occupational pesticide exposures are associated with AD. Previously, we reported that serum levels of dichlorodiphenyldichloroethylene (DDE), the metabolite of the pesticide dichlorodiphenyltrichloroethane (DDT), were elevated in a small number of patients with AD (n=20). OBJECTIVE To evaluate the association between serum levels of DDE and AD and whether the apolipoprotein E (APOE) genotype modifies the association. DESIGN, SETTING, AND PARTICIPANTS A case-control study consisting of existing samples from patients with AD and control participants from the Emory University Alzheimer's Disease Research Center and the University of Texas Southwestern Medical School's Alzheimer's Disease Center. Serum levels of DDE were measured in 79 control and 86 AD cases. MAIN OUTCOMES AND MEASURES Serum DDE levels, AD diagnosis, severity of AD measured by the Mini-Mental State Examination score, and interaction with APOE4 status. RESULTS Levels of DDE were 3.8-fold higher in the serum of those with AD (mean [SEM], 2.64 [0.35] ng/mg cholesterol) when compared with control participants (mean [SEM], 0.69 [0.1] ng/mg cholesterol; P < .001). The highest tertile of DDE levels was associated with an odds ratio of 4.18 for increased risk for AD (95% CI, 2.54-5.82; P < .001) and lower Mini-Mental State Examination scores (-1.605; range, -3.095 to -0.114; P < .0001). The Mini-Mental State Examination scores in the highest tertile of DDE were -1.753 points lower in the subpopulation carrying an APOE epsilon 4 allele compared with those carrying an APOE epsilon 3 allele (P interaction = .04). Serum levels of DDE were highly correlated with brain levels of DDE (rho = 0.95). Exposure of human neuroblastoma cells to DDT or DDE increased levels of amyloid precursor protein. CONCLUSIONS AND RELEVANCE Elevated serum DDE levels are associated with an increased risk for AD and carriers of an APOE4 epsilon 4 allele may be more susceptible to the effects of DDE. Both DDT and DDE increase amyloid precursor protein levels, providing mechanistic plausibility for the association of DDE exposure with AD. Identifying people who have elevated levels of DDE and carry an APOE epsilon 4 allele may lead to early identification of some cases of AD.
引用
收藏
页码:284 / 290
页数:7
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