Matches in SemOpenAlex for { <https://semopenalex.org/work/W2988092241> ?p ?o ?g. }
- W2988092241 endingPage "893" @default.
- W2988092241 startingPage "881" @default.
- W2988092241 abstract "Late life disability is a highly devastating condition affecting 20% or more of persons aged 65 years and older in the USA; it is an important determinant of acute medical and long-term care costs which represent a growing burden on national economies. Disability is a multifactorial trait that contributes substantially to decline of health/wellbeing. Accordingly, gaining insights into the genetics of disability could help in identifying molecular mechanisms of this devastating condition and age-related processes contributing to a large fraction of specific geriatric conditions, concordantly with geroscience. We performed a genome-wide association study of disability in a sample of 24,068 subjects from five studies with 12,550 disabled individuals. We identified 30 promising disability-associated polymorphisms in 19 loci at p < 10-4; four of them attained suggestive significance, p < 10-5. In contrast, polygenic risk scores aggregating effects of minor alleles of independent SNPs that were adversely or beneficially associated with disability showed highly significant associations in meta-analysis, p = 3.13 × 10-45 and p = 5.60 × 10-23, respectively, and were replicated in each study. The analysis of genetic pathways, related diseases, and biological functions supported the connections of genes for the identified SNPs with disabling and age-related conditions primarily through oxidative/nitrosative stress, inflammatory response, and ciliary signaling. We identified musculoskeletal system development, maintenance, and regeneration as important components of gene functions. The beneficial and adverse gene sets may be differently implicated in the development of musculoskeletal-related disability with the beneficial set characterized, e.g., by regulation of chondrocyte proliferation and bone formation, and the adverse set by inflammation and bone loss." @default.
- W2988092241 created "2019-11-22" @default.
- W2988092241 creator A5017898754 @default.
- W2988092241 creator A5018020035 @default.
- W2988092241 creator A5033445213 @default.
- W2988092241 creator A5041686825 @default.
- W2988092241 creator A5042526575 @default.
- W2988092241 creator A5045601093 @default.
- W2988092241 creator A5065315650 @default.
- W2988092241 creator A5085542503 @default.
- W2988092241 date "2019-11-09" @default.
- W2988092241 modified "2023-10-14" @default.
- W2988092241 title "Polygenic risk score for disability and insights into disability-related molecular mechanisms" @default.
- W2988092241 cites W135250288 @default.
- W2988092241 cites W1560571961 @default.
- W2988092241 cites W1579653634 @default.
- W2988092241 cites W1595993343 @default.
- W2988092241 cites W1786262212 @default.
- W2988092241 cites W1911986360 @default.
- W2988092241 cites W1965874850 @default.
- W2988092241 cites W1972825709 @default.
- W2988092241 cites W1977229794 @default.
- W2988092241 cites W1978597088 @default.
- W2988092241 cites W1984860579 @default.
- W2988092241 cites W1993614440 @default.
- W2988092241 cites W2001682695 @default.
- W2988092241 cites W2004002095 @default.
- W2988092241 cites W2006545529 @default.
- W2988092241 cites W2010384718 @default.
- W2988092241 cites W2014224356 @default.
- W2988092241 cites W2015850772 @default.
- W2988092241 cites W2021904780 @default.
- W2988092241 cites W2031027059 @default.
- W2988092241 cites W2032050435 @default.
- W2988092241 cites W2032276849 @default.
- W2988092241 cites W2033839954 @default.
- W2988092241 cites W2038739447 @default.
- W2988092241 cites W2039022968 @default.
- W2988092241 cites W2054164550 @default.
- W2988092241 cites W2058681554 @default.
- W2988092241 cites W2061539393 @default.
- W2988092241 cites W2064097480 @default.
- W2988092241 cites W2073930491 @default.
- W2988092241 cites W2074477571 @default.
- W2988092241 cites W2079078124 @default.
- W2988092241 cites W2081743406 @default.
- W2988092241 cites W2084900761 @default.
- W2988092241 cites W2111004587 @default.
- W2988092241 cites W2111222524 @default.
- W2988092241 cites W2128178335 @default.
- W2988092241 cites W2130532337 @default.
- W2988092241 cites W2133520037 @default.
- W2988092241 cites W2144779638 @default.
- W2988092241 cites W2156104506 @default.
- W2988092241 cites W2159531143 @default.
- W2988092241 cites W2161197885 @default.
- W2988092241 cites W2161633633 @default.
- W2988092241 cites W2164059021 @default.
- W2988092241 cites W2164672030 @default.
- W2988092241 cites W2167311298 @default.
- W2988092241 cites W2171480404 @default.
- W2988092241 cites W2171937401 @default.
- W2988092241 cites W2262829592 @default.
- W2988092241 cites W2280847375 @default.
- W2988092241 cites W2290627980 @default.
- W2988092241 cites W2312699414 @default.
- W2988092241 cites W2401201457 @default.
- W2988092241 cites W2401811918 @default.
- W2988092241 cites W2411890015 @default.
- W2988092241 cites W2468727035 @default.
- W2988092241 cites W2510973425 @default.
- W2988092241 cites W2516470530 @default.
- W2988092241 cites W2529610833 @default.
- W2988092241 cites W2553476569 @default.
- W2988092241 cites W2556505942 @default.
- W2988092241 cites W2740118744 @default.
- W2988092241 cites W2747265021 @default.
- W2988092241 cites W2768191269 @default.
- W2988092241 cites W2779963304 @default.
- W2988092241 cites W2785279167 @default.
- W2988092241 cites W2799986334 @default.
- W2988092241 cites W2887988655 @default.
- W2988092241 cites W2889631667 @default.
- W2988092241 cites W2915985519 @default.
- W2988092241 cites W2930984925 @default.
- W2988092241 cites W2938809349 @default.
- W2988092241 cites W2944377002 @default.
- W2988092241 cites W2947649347 @default.
- W2988092241 cites W2289177495 @default.
- W2988092241 doi "https://doi.org/10.1007/s11357-019-00125-8" @default.
- W2988092241 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6925082" @default.
- W2988092241 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31707593" @default.
- W2988092241 hasPublicationYear "2019" @default.
- W2988092241 type Work @default.
- W2988092241 sameAs 2988092241 @default.
- W2988092241 citedByCount "2" @default.
- W2988092241 countsByYear W29880922412023 @default.
- W2988092241 crossrefType "journal-article" @default.