Association of Neurocognitive and Physical Function With Gait Speed in Midlife

被引:113
作者
Rasmussen, Line Jee Hartmann [1 ,2 ]
Caspi, Avshalom [1 ,3 ,4 ,5 ]
Ambler, Antony [6 ]
Broadbent, Jonathan M. [7 ]
Cohen, Harvey J. [8 ,9 ,10 ]
d'Arbeloff, Tracy [1 ]
Elliott, Maxwell [1 ]
Hancox, Robert J. [11 ]
Harrington, HonaLee [1 ]
Hogan, Sean [6 ]
Houts, Renate [1 ]
Ireland, David [6 ]
Knodt, Annchen R. [1 ]
Meredith-Jones, Kim [6 ]
Morey, Miriam C. [8 ,10 ,12 ]
Morrison, Lynda [6 ]
Poulton, Richie [6 ]
Ramrakha, Sandhya [6 ]
Richmond-Rakerd, Leah [1 ,13 ]
Sison, Maria L. [1 ]
Sneddon, Kate [6 ]
Thomson, W. Murray [7 ]
Hariri, Ahmad R. [1 ]
Moffitt, Terrie E. [1 ,3 ,4 ,5 ]
机构
[1] Duke Univ, Dept Psychol & Neurosci, 2020 W Main St,Ste 201, Durham, NC 27708 USA
[2] Copenhagen Univ Hosp Amager & Hvidovre, Clin Res Ctr, Hvidovre, Denmark
[3] Duke Univ, Dept Psychiat & Behav Sci, Sch Med, Durham, NC 27708 USA
[4] Duke Univ, Ctr Genom & Computat Biol, Durham, NC 27708 USA
[5] Kings Coll London, Social Genet & Dev Psychiat Ctr, Inst Psychiat Psychol & Neurosci, London, England
[6] Univ Otago, Dept Psychol, Dunedin Multidisciplinary Hlth & Dev Res Unit, Dunedin, New Zealand
[7] Univ Otago, Dept Oral Sci, Dunedin, New Zealand
[8] Duke Univ, Claude D Pepper Older Amer Independence Ctr, Durham, NC 27708 USA
[9] Duke Univ, Duke Ctr Study Aging & Human Dev, Durham, NC 27708 USA
[10] Duke Univ, Dept Med, Durham, NC 27708 USA
[11] Univ Otago, Dunedin Sch Med, Dept Prevent & Social Med, Dunedin, New Zealand
[12] Durham VA Med Ctr, Geriatr Res Educ & Clin Ctr, Durham, NC USA
[13] Univ North Carolina Chapel Hill, Frank Porter Graham Child Dev Inst, Chapel Hill, NC USA
基金
美国国家卫生研究院; 英国医学研究理事会; 美国国家科学基金会;
关键词
NORMATIVE DATA; WALKING SPEED; OLDER-ADULTS; STRENGTH; BALANCE; SCORES; GRIP;
D O I
10.1001/jamanetworkopen.2019.13123
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
IMPORTANCE Gait speed is a well-known indicator of risk of functional decline and mortality in older adults, but little is known about the factors associated with gait speed earlier in life. OBJECTIVES To test the hypothesis that slow gait speed reflects accelerated biological aging at midlife, as well as poor neurocognitive functioning in childhood and cognitive decline from childhood to midlife. DESIGN, SETTING, AND PARTICIPANTS This cohort study uses data from the Dunedin Multidisciplinary Health and Development Study, a population-based study of a representative 1972 to 1973 birth cohort in New Zealand that observed participants to age 45 years (until April 2019). Data analysis was performed from April to June 2019. EXPOSURES Childhood neurocognitive functions and accelerated aging, brain structure, and concurrent physical and cognitive functions in adulthood. MAIN OUTCOMES AND MEASURES Gait speed at age 45 years, measured under 3 walking conditions: usual, dual task, and maximum gait speeds. RESULTS Of the 1037 original participants (91% of eligible births; 535 [51.6%] male), 997 were alive at age 45 years, of whom 904 (90.7%) had gait speed measured (455 [50.3%] male; 93% white). The mean (SD) gait speeds were 1.30 (0.17) m/s for usual gait, 1.16 (0.23) m/s for dual task gait, and 1.99 (0.29) m/s for maximum gait. Adults with more physical limitations (standardized regression coefficient [beta], -0.27; 95% CI, -0.34 to -0.21; P <.001), poorer physical functions (ie, weak grip strength [beta, 0.36; 95% CI, 0.25 to 0.46], poor balance [beta, 0.28; 95% CI, 0.21 to 0.34], poor visual-motor coordination [beta, 0.24; 95% CI, 0.17 to 0.30], and poor performance on the chair-stand [beta, 0.34; 95% CI, 0.27 to 0.40] or 2-minute step tests [beta, 0.33; 95% CI, 0.27 to 0.39]; all P < .001), accelerated biological aging across multiple organ systems (beta, -0.33; 95% CI, -0.40 to -0.27; P < .001), older facial appearance (beta, -0.25; 95% CI, -0.31 to -0.18; P < .001), smaller brain volume (beta, 0.15; 95% CI, 0.06 to 0.23; P < .001), more cortical thinning (beta, 0.09; 95% CI, 0.02 to 0.16; P=.01), smaller cortical surface area (beta, 0.13; 95% CI, 0.04 to 0.21; P=.003), and more white matter hyperintensities (beta, -0.09; 95% CI, -0.15 to -0.02; P=.01) had slower gait speed. Participants with lower IQ in midlife (beta, 0.38; 95% CI, 0.32 to 0.44; P < .001) and participants who exhibited cognitive decline from childhood to adulthood (beta, 0.10; 95% CI, 0.04 to 0.17; P < .001) had slower gait at age 45 years. Those with poor neurocognitive functioning as early as age 3 years had slower gait in midlife (beta, 0.26; 95% CI, 0.20 to 0.32; P < .001). CONCLUSIONS AND RELEVANCE Adults' gait speed is associated with more than geriatric functional status; it is also associated with midlife aging and lifelong brain health.
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页数:15
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