从成年早期到中年的多病轨迹与中年身体功能的关系。

C Barrett Bowling,Richard Sloane,Richard A Faldowski,Carl Pieper,Tyson Brown,Erin E Dooley,Brett T Burrows,Ankeet S Bhatt,Donald M Lloyd-Jones,Cora E Lewis,Kelley Pettee Gabriel
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引用次数: 0

摘要

背景:慢性疾病可以在成年早期发展,并以不同的速度积累。然而,青年时期多病轨迹组与中年身体机能之间的关系尚未得到很好的研究。方法数据来自2018名年轻人冠状动脉风险发展(CARDIA)研究参与者,他们完成了PROMIS功能短表和五项体能测试(步态速度、握力、平衡、椅子站立、6分钟步行,综合得分范围为0-20,越高越好)。先前使用潜在类别增长模型确定了多病轨迹组,并以发病年龄和条件积累速度为特征:(1)50岁出头,慢(E50S),(2) 45岁中期,快(M40F),(3) 35岁中期,快(M30F),(4) 20岁后期,慢(L20F),(5) 20岁中期,慢(M20S),(6) 20岁中期,快(M20F)。采用多元线性回归估计多病轨迹组与中年身体功能评分的相关性。结果测体功能时,参与者平均年龄(SD)为60.0(3.6)岁,女性占58.2%,黑人占44.4%。与E50S组相比,M40F组、M30F组、L20F组、M20F组的PROMIS评分调整后的平均差异分别为-1.37、-1.44、-3.18、-2.53 (p值均<0.01)。与E50S相比,L20F、M20S、M20F的综合性能评分调整后的平均差异分别为-1.48、-0.44、-1.51 (p值均<0.05)。结论从成年早期开始的慢性疾病发病早、积累快,可识别中年时功能受限的高危人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of multimorbidity trajectories from early adulthood through middle age with middle-age physical function.
BACKGROUND Chronic conditions can develop early in the adult life course and accumulate at different rates. However, the association between multimorbidity trajectory groups from young adulthood and physical function in midlife has not been well studied. METHODS Data are from 2,018 Coronary Artery Risk Development in Young Adults (CARDIA) study participants who completed a PROMIS Function Short Form and five physical performance tests (gait speed, grip strength, balance, chair stands, 6-minute-walk, composite score range 0-20, higher is better). Multimorbidity trajectory groups were previously identified using latent class growth models and characterized by the age of onset and rapidity of accumulation of conditions: (1) early-fifties, slow (E50S), (2) mid-forties, fast (M40F), (3) mid-thirties, fast (M30F), (4) late-twenties, slow (L20F), (5) mid-twenties, slow (M20S), and (6) mid-twenties, fast (M20F). The association of multimorbidity trajectory group with physical function scores in middle age were estimated using multiple linear regression. RESULTS At the time of physical function measurement, participants had a mean age (SD) of 60.0 (3.6) years, 58.2% were female, and 44.4% were Black. Compared to participants in the E50S class, adjusted mean differences in the PROMIS score were -1.37, -1.44, -3.18, and -2.53 for those in the M40F, M30F, L20F, M20F, respectively (all p-values <0.01). Compared to E50S adjusted mean differences in the composite performance scores were -1.48, -0.44, and -1.51 for L20F, M20S, M20F, respectively (all p-values <0.05). CONCLUSIONS Earlier onset and more rapid accumulation of chronic conditions from early adulthood may identify those at risk for functional limitations in midlife.
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