Journal of Cachexia, Sarcopenia and Muscle (Jun 2022)

Handgrip strength and all‐cause dementia incidence and mortality: findings from the UK Biobank prospective cohort study

  • Irene Esteban‐Cornejo,
  • Frederick K. Ho,
  • Fanny Petermann‐Rocha,
  • Donald M. Lyall,
  • David Martinez‐Gomez,
  • Verónica Cabanas‐Sánchez,
  • Francisco B. Ortega,
  • Charles H. Hillman,
  • Jason M.R. Gill,
  • Terence J. Quinn,
  • Naveed Sattar,
  • Jill P. Pell,
  • Stuart R. Gray,
  • Carlos Celis‐Morales

DOI
https://doi.org/10.1002/jcsm.12857
Journal volume & issue
Vol. 13, no. 3
pp. 1514 – 1525

Abstract

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Abstract Background This study aimed to investigate the associations of grip strength with incidence and mortality from dementia and whether these associations differ by sociodemographic and lifestyle factors. Methods A total of 466 788 participants of the UK Biobank (median age 56.5 years, 54.5% women). The outcome was all‐cause dementia incidence and mortality and the exposure was grip strength. Grip strength was assessed using a Jamar J00105 hydraulic hand dynamometer. Results Excluding the first 2 years of follow‐up (landmark analysis), mean follow‐up was 9.1 years (inter‐quartile range: 8.3; 9.7) for incidence and 9.3 (inter‐quartile range: 8.7; 10.0) for mortality. During this time, 4087 participants developed dementia, and 1309 died from it. Lower grip strength was associated with a higher risk of dementia incidence and mortality independent of major confounding factors (P < 0.001). Individuals in the lowest quintile of grip strength had 72% [95% confidence interval (CI): 1.55; 1.92] higher incident dementia risk and 87% [95% CI: 1.55; 2.26] higher risk of dementia mortality compared with those in the highest quintile. Our PAF analyses indicate that 30.1% of dementia cases and 32.3% of dementia deaths are attributable to having low grip strength. The association between grip strength and dementia outcomes did not differ by lifestyle or sociodemographic factors. Conclusions Lower grip strength was associated with a higher risk of all‐cause dementia incidence and mortality, independently of important confounding factors.

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