Abdominal Visceral Adipose Tissue and All-Cause Mortality: A Systematic Review.

Front Endocrinol (Lausanne)

Calcium Metabolism and Osteoporosis Program, World Health Organization (WHO) Collaborating Center for Metabolic Bone Disorders, Division of Endocrinology and Metabolism, Department of Internal Medicine - American University of Beirut Medical Center, Beirut, Lebanon.

Published: September 2022

AI Article Synopsis

  • Increased abdominal visceral adipose tissue (VAT) is linked to a higher risk of all-cause mortality, particularly in individuals aged 65 and younger, based on data from 12 cohorts.
  • The association diminishes when controlling for metabolic factors like body mass index and glycemic levels.
  • In older adults, the relationship with mortality risks is inconsistent and may even reverse, suggesting that further detailed analysis is necessary to understand these dynamics better.

Article Abstract

Introduction: Increased abdominal visceral adipose tissue (VAT) implies an adverse cardio-metabolic profile. We examined the association of abdominal VAT parameters and all-cause mortality risk.

Methods: We systematically searched four databases. We performed citations/articles screening, data abstraction, and quality assessment in duplicate and independently (CRD42020205021).

Results: We included 12 cohorts, the majority used computed tomography to assess abdominal VAT area. Six cohorts with a mean age ≤ 65 years, examining all-cause mortality risk per increment in VAT area (cm) or volume (cm), showed a 11-98% relative risk increase with higher VAT parameters. However, the association lost significance after adjusting for glycemic indices, body mass index, or other fat parameters. In 4 cohorts with a mean age >65 years, the findings on mortality were inconsistent. Conversely, in two cohorts (mean age 73-77 years), a higher VAT density, was inversely proportional to VAT area, and implied a higher mortality risk.

Conclusion: A high abdominal VAT area seems to be associated with increased all-cause mortality in individuals ≤ 65 years, possibly mediated by metabolic complications, and not through an independent effect. This relationship is weaker and may reverse in older individuals, most likely secondary to confounding bias and reverse causality. An individual participant data meta-analysis is needed to confirm our findings, and to define an abdominal VAT area cutoff implying increased mortality risk.

Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=205021, identifier CRD42020205021.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446237PMC
http://dx.doi.org/10.3389/fendo.2022.922931DOI Listing

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