Telomere length and brain imaging phenotypes in UK Biobank

被引:18
|
作者
Topiwala, Anya C. [1 ]
Nichols, Thomas [1 ,2 ]
Williams, Logan Z. J. [3 ]
Robinson, Emma [3 ]
Alfaro-Almagro, Fidel P. [4 ]
Taschler, Bernd L. [4 ]
Wang, Chaoyue [5 ]
Nelson, Christopher J. [6 ,7 ]
Miller, Karla M. [5 ]
Codd, Veryan [6 ,7 ]
Samani, Nilesh [6 ,7 ]
Smith, Stephen [5 ]
机构
[1] Univ Oxford, Big Data Inst, Nuffield Dept Populat Hlth, Oxford, England
[2] Univ Oxford, Wellcome Ctr Integrat Neuroimaging, Nuffield Dept Clin Neurosci, FMRIB, Oxford, England
[3] Kings Coll London, Ctr Developing Brain, Sch Biomed Engn & Imaging Sci, London, England
[4] Univ Oxford, Wellcome Ctr Integrat Neuroimaging WIN FMRIB, Nuffield Dept Clin Neurosci, Oxford, England
[5] Univ Oxford, Wellcome Ctr Integrat Neuroimaging WIN FMRIB, Oxford, England
[6] Univ Leicester, Dept Cardiovasc Sci, Leicester, England
[7] Glenfield Hosp, NIHR Leicester Biomed Res Ctr, Leicester, England
来源
PLOS ONE | 2023年 / 18卷 / 03期
基金
英国惠康基金; 英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
ALZHEIMERS ASSOCIATION WORKGROUPS; INDEPENDENT COMPONENT ANALYSIS; WHITE-MATTER; MOTOR NETWORK; FUNCTIONAL CONNECTIVITY; RESTING-STATE; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; COGNITIVE DECLINE; QUALITY-CONTROL;
D O I
10.1371/journal.pone.0282363
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Telomeres form protective caps at the ends of chromosomes, and their attrition is a marker of biological aging. Short telomeres are associated with an increased risk of neurological and psychiatric disorders including dementia. The mechanism underlying this risk is unclear, and may involve brain structure and function. However, the relationship between telomere length and neuroimaging markers is poorly characterized. Here we show that leucocyte telomere length (LTL) is associated with multi-modal MRI phenotypes in 31,661 UK Biobank participants. Longer LTL is associated with: i) larger global and subcortical grey matter volumes including the hippocampus, ii) lower T1-weighted grey-white tissue contrast in sensory cortices, iii) white-matter microstructure measures in corpus callosum and association fibres, iv) lower volume of white matter hyperintensities, and v) lower basal ganglia iron. Longer LTL was protective against certain related clinical manifestations, namely all-cause dementia (HR 0.93, 95% CI: 0.91-0.96), but not stroke or Parkinson's disease. LTL is associated with multiple MRI endophenotypes of neurodegenerative disease, suggesting a pathway by which longer LTL may confer protective against dementia.
引用
收藏
页数:17
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