The burden of cardiovascular disease attributable to high fasting plasma glucose:Findings from the global burden of disease study 2019

Diabetes Metab Syndr. 2024 May;18(5):103025. doi: 10.1016/j.dsx.2024.103025. Epub 2024 May 7.

Abstract

Aim: High fasting plasma glucose (HFPG) is a key risk factor for cardiovascular disease (CVD). Few studies have evaluated the CVD burden attributable to HFPG globally. It is urgent to investigate the current epidemiological pattern and past trends of CVD attributable to HFPG.

Methods: We used the Global Burden of Disease Study (GBD) 2019 to describe the CVD burden attributable to HFPG in 2019 and evaluate temporal trends between 1990 and 2019.

Results: Global Disability-Adjusted Life Years (DALYs) cases and death cases of HFPG-related CVD were approximately 72,591,163 and 3,763,298 in 2019, with an increase of 107.4 % and 114.6 % compared with 1990, respectively. Despite the increases, the age-standardized DALYs rate (ASDAR) and age-standardized death rate (ASDR) of HFPG-related CVD contributed to 895.2 per 100,000 people and 48.4 per 100,000 people in 2019, with an estimated annual percentage change (EAPC) of -0.22 and -0.31, respectively, from 1990. The highest ASDAR and ASDR of HFPG-related CVD were in 2019 observed in the low-middle SDI (Socio-demographic Index) and middle-SDI regions. Low SDI and some low-middle SDI regions showed an increase in ASDAR and ASDR of HFPG-related CVD from 1990 to 2019. Males are more affected by HFPG-related CVD than females across all years. The CVD burden attributable to HFPG in the elderly are higher than those in the young in 2019. The main causes of the global CVD burden attributable to HFPG in 2019 were ischemic heart disease, stroke, and peripheral arterial disease.

Conclusion: The CVD burden attributable to HFPG remains a serious public health challenge threatening human health worldwide. It is necessary to develop more targeted and specific strategies to reduce CVD burden attributable to HFPG, especially in males, elderly, and lower SDI regions.

Keywords: Cardiovascular disease; Deaths; Disability-Adjusted Life Years; Global burden of disease study; High fasting plasma glucose.

MeSH terms

  • Adult
  • Aged
  • Blood Glucose* / analysis
  • Cardiovascular Diseases* / epidemiology
  • Cardiovascular Diseases* / etiology
  • Cost of Illness
  • Fasting* / blood
  • Female
  • Follow-Up Studies
  • Global Burden of Disease*
  • Humans
  • Male
  • Middle Aged
  • Prognosis
  • Risk Factors
  • Young Adult

Substances

  • Blood Glucose