Past adult lead exposure is linked to neurodegeneration measured by brain MRI

被引:126
|
作者
Stewart, W. F.
Schwartz, B. S.
Davatzikos, C.
Shen, D.
Liu, D.
Wu, X.
Todd, A. C.
Shi, W.
Bassett, S.
Youssem, D.
机构
[1] Geisinger Med Clin, Geisinger Hlth Syst, Ctr Hlth Res & Rural Advocacy, Danville, PA 17822 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD USA
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[4] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[5] Mt Sinai Sch Med, Dept Community & Prevent Med, New York, NY USA
[6] Johns Hopkins Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD USA
[7] Johns Hopkins Sch Med, Dept Psychiat, Baltimore, MD USA
关键词
D O I
10.1212/01.wnl.0000216138.69777.15
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine whether cumulative lead dose in former organolead workers was associated with MRI measures of white matter lesions (WML) and global and structure-specific brain volumes. Methods: MRIs, tibia lead, and other measures were obtained from 532 former organolead workers with a mean age of 56 years and a mean of 18 years since last occupational exposure to lead. Cumulative lead dose was measured by tibia lead, obtained by X-ray fluorescence, and expressed as mu g lead per gram of bone mineral (mu g Pb/g). WML were evaluated using the Cardiovascular Health Study grading scale. A total of 21 global and specific brain regions were evaluated. Results: A total of 36% of individuals had WML grade of 1 to 7 ( 0 to 9 scale). Increasing peak tibia lead was associated with increasing WML grade (p = 0.004). The adjusted OR for a 1 mu g Pb/g increase in tibia lead was 1.042 (95% CI = 1.021, 1.063) for a CHS grade of 5 + (>= 5 vs < 5). In linear regression, the coefficient for tibia lead was negative for associations with all structures. Higher tibia lead was significantly related to smaller total brain volume, frontal and total gray matter volume, and parietal white matter volume. Of nine smaller specific regions of interest, higher tibia lead was associated with smaller volumes for the cingulate gyrus and insula. Conclusions: These data suggest that cumulative lead dose is associated with persistent brain lesions, and may explain previous findings of a progressive decline in cognitive function.
引用
收藏
页码:1476 / 1484
页数:9
相关论文
共 50 条
  • [41] Developmental lead exposure impairs contextual fear conditioning and reduces adult hippocampal neurogenesis in the rat brain
    Jaako-Movits, K
    Zharkovsky, T
    Romantchik, O
    Jurgenson, M
    Merisalu, E
    Heidmets, LT
    Zharkovsky, A
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2005, 23 (07) : 627 - 635
  • [42] PRENATAL ETHANOL EXPOSURE ALTERS BRAIN CONNECTIVY IN ADULT RATS: A RESTING STATE FUNCTIONAL MRI STUDY
    Tang, S.
    Xu, S.
    Waddell, J.
    Hanscom, M.
    Zhu, W.
    Mooney, S. M.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2017, 41 : 131A - 131A
  • [43] Baby teeth reveal children's past lead exposure
    Gammon, Katharine
    CHEMICAL & ENGINEERING NEWS, 2019, 97 (22) : 7 - 7
  • [44] Cardiovascular MRI traits are genetically linked to brain pathophysiology
    Papatriantafyllou, Maria
    NATURE CARDIOVASCULAR RESEARCH, 2023, 2 (07): : 602 - 602
  • [45] Cardiovascular MRI traits are genetically linked to brain pathophysiology
    Maria Papatriantafyllou
    Nature Cardiovascular Research, 2023, 2 : 602 - 602
  • [46] A β-synuclein mutation linked to dementia produces neurodegeneration when expressed in mouse brain
    Fujita, Masayo
    Sugama, Shuei
    Sekiyama, Kazunari
    Sekigawa, Akio
    Tsukui, Tohru
    Nakai, Masaaki
    Waragai, Masaaki
    Takenouchi, Takato
    Takamatsu, Yoshiki
    Wei, Jianshe
    Rockenstein, Edward
    LaSpada, Albert R.
    Masliah, Eliezer
    Inoue, Satoshi
    Hashimoto, Makoto
    NATURE COMMUNICATIONS, 2010, 1
  • [47] A β-synuclein mutation linked to dementia produces neurodegeneration when expressed in mouse brain
    Masayo Fujita
    Shuei Sugama
    Kazunari Sekiyama
    Akio Sekigawa
    Tohru Tsukui
    Masaaki Nakai
    Masaaki Waragai
    Takato Takenouchi
    Yoshiki Takamatsu
    Jianshe Wei
    Edward Rockenstein
    Albert R. LaSpada
    Eliezer Masliah
    Satoshi Inoue
    Makoto Hashimoto
    Nature Communications, 1
  • [48] Role of early life exposure and environment on neurodegeneration: Implications on brain disorders
    Modgil S.
    Lahiri D.K.
    Sharma V.L.
    Anand A.
    Translational Neurodegeneration, 3 (1)
  • [49] Editorial: New Insights Into Adult Neurogenesis and Neurodegeneration: Challenges for Brain Repair
    Morales-Garcia, Jose A.
    Kaneko, Naoko
    Herranz-Perez, Vicente
    FRONTIERS IN NEUROSCIENCE, 2022, 16