Association of Childhood Lead Exposure With MRI Measurements of Structural Brain Integrity in Midlife

被引:42
|
作者
Reuben, Aaron [1 ]
Elliott, Maxwell L. [1 ]
Abraham, Wickliffe C. [2 ]
Broadbent, Jonathan [3 ]
Houts, Renate M. [1 ]
Ireland, David [4 ]
Knodt, Annchen R. [1 ]
Poulton, Richie [4 ]
Ramrakha, Sandhya [4 ]
Hariri, Ahmad R. [1 ]
Caspi, Avshalom [1 ,5 ,6 ,7 ,8 ]
Moffitt, Terrie E. [1 ,5 ,6 ,7 ,8 ]
机构
[1] Duke Univ, Dept Psychol & Neurosci, 417 Chapel Dr, Durham, NC 27708 USA
[2] Univ Otago, Brain Hlth Res Ctr, Brain Res New Zealand, Dept Psychol, Dunedin, New Zealand
[3] Univ Otago, Sir John Walsh Res Inst, Fac Dent, Dunedin, New Zealand
[4] Univ Otago, Dept Psychol, Dunedin Multidisciplinary Hlth & Dev Res Unit, Dunedin, New Zealand
[5] Duke Univ, Ctr Genom & Computat Biol, Durham, NC USA
[6] Duke Univ, Dept Psychiat & Behav Sci, Durham, NC USA
[7] Kings Coll London, Social Genet & Dev Psychiat Ctr, Inst Psychiat Psychol & Neurosci, London, England
[8] Univ Oslo, Dept Psychol, PROMENTA, Oslo, Norway
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2020年 / 324卷 / 19期
基金
英国医学研究理事会;
关键词
BLOOD LEAD; COGNITIVE FUNCTION; ALZHEIMER-DISEASE; DECLINE; AGE; POPULATION; DEMENTIA; CHILDREN; DUNEDIN; HEALTH;
D O I
10.1001/jama.2020.19998
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Importance Childhood lead exposure has been linked to disrupted brain development, but long-term consequences for structural brain integrity are unknown. Objective To test the hypothesis that childhood lead exposure is associated with magnetic resonance imaging (MRI) measurements of lower structural integrity of the brain in midlife. Design, Setting, and Participants The Dunedin Study followed a population-representative 1972-1973 birth cohort in New Zealand (N = 564 analytic sample) to age 45 years (until April 2019). Exposures Childhood blood lead levels measured at age 11 years. Main Outcomes and Measures Structural brain integrity at age 45 years assessed via MRI (primary outcomes): gray matter (cortical thickness, surface area, hippocampal volume), white matter (white matter hyperintensities, fractional anisotropy [theoretical range, 0 {diffusion is perfectly isotropic} to 100 {diffusion is perfectly anisotropic}]), and the Brain Age Gap Estimation (BrainAGE), a composite index of the gap between chronological age and a machine learning algorithm-estimated brain age (0 indicates a brain age equivalent to chronological age; positive and negative values represent an older and younger brain age, respectively). Cognitive function at age 45 years was assessed objectively via the Wechsler Adult Intelligence Scale IV (IQ range, 40-160, standardized to a mean of 100 [SD, 15]) and subjectively via informant and self-reports (z-score units; scale mean, 0 [SD, 1]). Results Of 1037 original participants, 997 were alive at age 45 years, of whom 564 (57%) had received lead testing at age 11 years (302 [54%] male) (median follow-up, 34 [interquartile range, 33.7-34.7] years). Mean blood lead level at age 11 years was 10.99 (SD, 4.63) mu g/dL. After adjusting for covariates, each 5-mu g/dL higher childhood blood lead level was significantly associated with 1.19-cm(2) smaller cortical surface area (95% CI, -2.35 to -0.02 cm(2); P = .05), 0.10-cm(3) smaller hippocampal volume (95% CI, -0.17 to -0.03 cm(3); P = .006), lower global fractional anisotropy (b = -0.12; 95% CI, -0.24 to -0.01; P = .04), and a BrainAGE index 0.77 years older (95% CI, 0.02-1.51 years; P = .05) at age 45 years. There were no statistically significant associations between blood lead level and log-transformed white matter hyperintensity volume (b = 0.05 log mm(3); 95% CI, -0.02 to 0.13 log mm(3); P = .17) or mean cortical thickness (b = -0.004 mm; 95% CI, -0.012 to 0.004 mm; P = .39). Each 5-mu g/dL higher childhood blood lead level was significantly associated with a 2.07-point lower IQ score at age 45 years (95% CI, -3.39 to -0.74; P = .002) and a 0.12-point higher score on informant-rated cognitive problems (95% CI, 0.01-0.23; P = .03). There was no statistically significant association between childhood blood lead levels and self-reported cognitive problems (b = -0.02 points; 95% CI, -0.10 to 0.07; P = .68). Conclusions and Relevance In this longitudinal cohort study with a median 34-year follow-up, higher childhood blood lead level was associated with differences in some MRI measures of brain structure that suggested lower structural brain integrity in midlife. Because of the large number of statistical comparisons, some findings may represent type I error. This study examines the association of blood lead levels in childhood with MRI measures of brain integrity as well as cognitive function assessments at age 45 years in a New Zealand birth cohort. Question Is childhood lead exposure associated with differences in magnetic resonance imaging (MRI) measurements of the integrity of brain structure in midlife? Findings In this longitudinal prospective cohort study of 564 New Zealand children followed up to midlife, greater lead exposure in childhood was significantly associated with differences in MRI measurements of brain structure at age 45 years, including smaller cortical surface area, smaller hippocampal volume, lower global fractional anisotropy, and an older estimated brain age. Meaning Higher childhood blood lead level was associated with differences in MRI measurements of brain structure that suggested lower structural brain integrity in midlife.
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收藏
页码:1970 / 1979
页数:10
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