The relationship between muscular atrophy/sarcopenia and cardiovascular diseases in the elderly: a bibliometrics

Zhisheng Tan1, Yunchun Zhao1, Zhengmin Jin1

  • 1Cadre Ward, 920th Hospital of Joint Logistics Support Force of PLA, Kunming, China.

Insights

Cardiovascular diseases increase the risk of muscular atrophy and sarcopenia in older adults. Further research is needed to understand mechanisms and develop prevention strategies for these age-related conditions.

Area of Science:

  • Geriatrics
  • Cardiovascular Medicine
  • Aging Research

Background:

  • Global aging population drives increased prevalence of cardiovascular diseases and sarcopenia.
  • Cardiovascular diseases are significant risk factors for muscular atrophy and sarcopenia in the elderly.
  • These conditions contribute to increased patient disability and mortality.

Purpose of the Study:

  • To analyze the existing literature on the relationship between cardiovascular diseases and muscular atrophy/sarcopenia in the aging population.
  • To identify key research trends, contributing countries, and influential publications in this field.

Main Methods:

  • Literature search of the Science Citation Index Expanded (SCI-E) database (1900-March 14, 2021).
  • Keywords used: "muscular atrophy" OR "sarcopenia" and "cardiovascular diseases" OR "cardiac & cardiovascular systems".
  • Bibliometric analysis using CiteSpace software for publication trends, country/institution contributions, and author/keyword analysis.

Main Results:

  • 1,004 documents analyzed with 26,705 citations.
  • Top publishing countries: United States, Japan, Germany, South Korea, Italy.
  • Limited international research cooperation observed; focus on mortality risk and geriatric journals.

Conclusions:

  • The link between muscular atrophy/sarcopenia and cardiovascular diseases is a significant area of geriatric and cardiovascular research.
  • Further investigation into underlying mechanisms is essential.
  • Development of effective prevention strategies is warranted.
Abstract

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