부산대학교 도서관

Background: Understanding the pathologic bases underlying the heterogeneity of motor decline in old age may lead to targeted treatments. We examined whether different brain pathologies are related to declining grip strength and gait function.Methods: We examined postmortem brains of older adults who underwent annual motor testing. Postmortem exam measured six neurodegenerative and five cerebrovascular disease (CVD) pathologies. Grip strength was measured twice bilaterally using a hand-held dynamometer and gait function was a composite measure based on time and steps taken to walk 8 ft and perform a 360 o turn twice.Results: In separate linear mixed effects models including all autopsied adults (N=1217), neurodegenerative pathologies including tau tangles, TDP-43, and nigral neuronal loss were associated with declining grip strength, but not CVD pathologies. In contrast, while both CVD and neurodegenerative pathologies were associated with declining gait function, CVD pathologies accounted for 75% of the variance of declining rate of gait function explained by brain pathologies and neurodegenerative pathologies accounted for 25%. These findings were unchanged in adults (n=970) without a history of stroke. Restricting analyses to only adults without dementia (n=661), CVD pathologies continued to account for the majority of the variance of declining gait. However, we failed to detect in this subgroup variance of declining grip strength explained by neurodegenerative or CVD pathologies.Conclusion: Different pathologies accumulating in aging brains may contribute to the phenotypic heterogeneity of motor decline. Larger studies are needed in older adults without dementia to assess differences in the motor consequences of varied brain pathologies. [ABSTRACT FROM AUTHOR]