Eight-Year Changes in Multimorbidity and Frailty in Adults With Type 2 Diabetes Mellitus: Associations With Cognitive and Physical Function and Mortality

Author:

Espeland Mark A12ORCID,Justice Jamie Nicole1ORCID,Bahnson Judy2,Evans Joni K2,Munshi Medha3,Hayden Kathleen M4ORCID,Simpson Felicia R5,Johnson Karen C6ORCID,Johnston Craig7,Kritchevsky Stephen R1ORCID

Affiliation:

1. Sticht Center for Healthy Aging and Alzheimer’s Prevention, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

2. Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

3. Joslin Geriatric Diabetes Program, Joslin Diabetes Center, Boston, Massachusetts, USA

4. Department of Social Sciences and Health Policy, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA

5. Department of Mathematics, Winston-Salem State University, Winston-Salem, North Carolina, USA

6. Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, Tennessee, USA

7. Department of Health and Human Performance, University of Houston, Houston, Texas, USA

Abstract

Abstract Background Indices of multimorbidity and deficit accumulation (ie, frailty indices) have been proposed as markers of biological aging. If true, changes in these indices over time should predict downstream changes in cognition and physical function, and mortality. Methods We examined associations that 8-year changes in (i) a multimorbidity index comprised of 9 chronic diseases and (ii) a frailty index (FI) based on deficit accumulation in functional, behavioral, and clinical characteristics had with subsequent measures of cognitive and physical function over 10 years. We drew data from 3 842 participants in the Action for Health in Diabetes clinical trial. They were aged 45–76 years at baseline and at risk for accelerated biological aging due to overweight/obesity and type 2 diabetes mellitus. Results A total of 1 501 (39%) of the cohort had 8-year increases of 1 among the 9 diseases tracked in the multimorbidity index and 868 (23%) had increases of ≥2. Those with greatest increases in multimorbidity tended to be older individuals, males, and non-Hispanic Whites. Greater FI increases tended to occur among individuals who were older, non-Hispanic White, heavier, and who had more baseline morbidities. Changes in multimorbidity and FI were moderately correlated (r = 0.26; p < .001). Increases in both multimorbidity and FI were associated with subsequently poorer composite cognitive function and 400-m walk speed and increased risk for death (all p < .001). Conclusions Accelerated biological aging, as captured by multimorbidity and frailty indices, predicts subsequent reduced function and mortality. Whether intensive lifestyle interventions generally targeting multimorbidity and FI reduce risks for downstream outcomes remains to be seen. Clinical Trials Registration Number: NCT00017953

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

National Institutes of Health

U.S. Department of Health and Human Services

National Institute on Aging

Glenn Foundation for Medical Research

Wake Forest Older Americans Independence Center

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing

Reference37 articles.

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