Kidney function predicts the rate of bone loss in older individuals: the Cardiovascular Health Study

Linda F Fried1, Michael G Shlipak, Catherine Stehman-Breen

  • 1VA Pittsburgh Healthcare System, Pittsburgh, PA 15240, USA. linda.fried@med.va.gov

Insights

Kidney dysfunction, indicated by cystatin-C levels, is linked to faster bone mineral density (BMD) loss at the hip, particularly in men. Further research is needed to confirm these findings and assess fracture risk. Keywords: kidney function, bone mineral density, cystatin-C, men.

Area of Science:

  • Gerontology
  • Nephrology
  • Orthopedics

Background:

  • Conflicting results exist regarding the association between kidney function and bone mineral density (BMD).
  • Cystatin-C, a novel kidney function marker independent of lean mass, was investigated.
  • The study focused on a population-based cohort of adults aged 65 years and older.

Purpose of the Study:

  • To examine the association of cystatin-C with initial and follow-up BMD.
  • To investigate the relationship between kidney function and bone loss in older adults.
  • To determine if cystatin-C is a predictor of BMD changes.

Main Methods:

  • Ancillary study of the Cardiovascular Health Study cohort.
  • Measurement of cystatin-C and covariates, followed by dual-energy x-ray absorptiometry for BMD.
  • Linear regression analysis of cystatin-C with initial BMD and annual BMD change at the hip, stratified by sex.

Main Results:

  • In 1519 participants, cystatin-C was marginally associated with initial BMD in men but not women.
  • Cystatin-C was associated with increased bone loss at the hip in men.
  • After adjusting for weight loss, cystatin-C was not significantly associated with bone loss in women.

Conclusions:

  • Kidney dysfunction, assessed by cystatin-C, correlates with accelerated hip BMD loss, especially in men.
  • These findings suggest a link between impaired kidney function and skeletal health.
  • Further investigation is required to validate these results and their implications for fracture risk.
Abstract

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