Extreme exercise in males is linked to mTOR signalling and onset of amyotrophic lateral sclerosis

肌萎缩侧索硬化 心肺适能 医学 孟德尔随机化 神经保护 神经科学 疾病 物理医学与康复 心理学 生物信息学 内科学 生物 遗传变异 基因 遗传学 基因型
作者
David O’Brien,Elham Alhathli,Ceryl A. Harwood,Debarati Bhattacharya,Kriti Gupta,Thomas Julian,Marcel Weinreich,Ryan J. H. West,Dennis Wang,Ross P. Byrne,Russell L. McLaughlin,Joanne Wuu,Michael Benatar,Johnathan Cooper‐Knock,Pamela J. Shaw
出处
期刊:Brain [Oxford University Press]
卷期号:148 (10): 3652-3664 被引量:1
标识
DOI:10.1093/brain/awaf235
摘要

Abstract Amyotrophic lateral sclerosis (ALS) is thought to be caused by interaction between genetic and environmental factors leading to motor neuron (MN) degeneration. Physical exercise has been linked to ALS but controversy remains. A key question is to determine which individuals might be at risk of exercise-associated ALS, because unnecessary avoidance of exercise could be harmful. We implemented complementary strategies including Mendelian randomization (MR) and multiple questionnaire-based measures of physical exercise in different cohorts. We include a prospective study involving UK Biobank participants where we could test for a relationship between exercise and the timing of future ALS symptom onset. To interrogate the molecular basis of our observations we performed a genetic association study of ‘extreme’ exercise, equivalent to >6 h of strenuous exercise or >12 h of any leisure-time exercise per week. Our data suggest that the link between increased physical exercise and ALS is particularly important for males who perform the most activity; with no evidence of a link in females. We determined that extreme exercise in males is associated with loss-of-function genetic variants within a number of mammalian target of rapamycin (mTOR) signalling genes that are also differentially expressed in ALS spinal cord. Activity-induced mTOR signalling has been shown to selectively benefit MN. Therefore, our findings could imply that moderate exercise is neuroprotective via enhanced mTOR signalling, but extreme exercise in men is associated with neurotoxicity and ALS via a failure of this mechanism. There was no significant overlap between genes associated with extreme exercise and those associated with ALS risk, consistent with a true gene–environment interaction rather than a shared genetic basis. We are not yet able to make individual-level recommendations regarding exercise and risk of ALS, but our conclusions should provide focus for future investigation.
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