Catechol‐O‐Methyltransferase Genotype, Frailty, and Gait Speed in a Biracial Cohort of Older Adults

Mance, Shannon; Rosso, Andrea L.; Bis, Joshua C.; Studenski, Stephanie A.; Bohnen, Nicolaas I.; Rosano, Caterina

doi:10.1111/jgs.16842

Cited by 1 publication

(1 citation statement)

References 36 publications

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“…Our study also found that components of frailty, including exhaustion, low physical activity, slow gait speed, and low grip strength may correlate with PD. A study investigated that in the frailty population, dopamine-related genotype has a stronger association with slow gait speed, which is not driven by the extreme gait slowing among frailty . A probable explanation is that frailty may trigger dopamine-related genotypes to develop PD.…”

Section: Discussionmentioning

confidence: 99%

Physical Frailty, Genetic Predisposition, and Incident Parkinson Disease

Zhang

Rong

et al. 2023

JAMA Neurol

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ImportanceCross-sectional evidence implicates high prevalent frailty in patients with Parkinson disease (PD), whereas the longitudinal association remains unknown.ObjectivesTo examine the longitudinal association of the frailty phenotype with the development of PD and to explore the modification role of genetic risk of PD in such an association.Design, Setting, and ParticipantsThis prospective cohort study launched in 2006 to 2010 with a follow-up of 12 years. Data were analyzed from March 2022 to December 2022. The UK Biobank recruited over 500 000 middle-aged and older adults from 22 assessment centers across the United Kingdom. Participants who were younger than 40 years (n = 101), diagnosed with dementia or PD at baseline, and developed dementia, PD, or died within 2 years from baseline were excluded (n = 4050). Participants who had no genetic data or mismatch between genetic sex and reported gender (n = 15 350), were not of self-reported British White descent (n = 27 850), and had no data for frailty assessment (n = 100 450) or any covariates were also excluded (n = 39 706). The final analysis included 314 998 participants.ExposuresThe physical frailty was assessed by the Fried criteria’s frailty phenotype through 5 domains, ie, weight loss, exhaustion, low physical activity, slow walking speed, and low grip strength. The polygenic risk score (PRS) for PD comprised 44 single-nucleotide variants.Main Outcomes and MeasuresNew-onset PD was identified through the hospital admission electronic health records and death register.ResultsAmong 314 998 participants (mean age, 56.1 years; 49.1% male), 1916 new-onset PD cases were documented. Compared with nonfrailty, the hazard ratio (HR) of incident PD in prefrailty and frailty was 1.26 (95% CI, 1.15-1.39) and 1.87 (95% CI, 1.53-2.28), respectively, and the absolute rate difference per 100 000 person-years was 1.6 (95% CI, 1.0-2.3) for prefrailty and 5.1 (95% CI, 2.9-7.3) for frailty. Exhaustion (HR, 1.41; 95% CI, 1.22-1.62), slow gait speed (HR, 1.32; 95% CI, 1.13-1.54), low grip strength (HR, 1.27; 95% CI, 1.13-1.43), and low physical activity (HR, 1.12; 95% CI, 1.00-1.25) were associated with incident PD. A significant interaction between frailty and PRS on PD was found and the highest hazard was observed in participants with frailty and high genetic risk.Conclusions and RelevancePhysical prefrailty and frailty were associated with incident PD independent of sociodemographic factors, lifestyles, multiple morbidities, and genetic background. These findings may have implications for the assessment and management of frailty for PD prevention.

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Section: Discussionmentioning

confidence: 99%