Skip to main navigation Skip to search Skip to main content

The age-specific quantitative effects of metabolic risk factors on cardiovascular diseases and diabetes: A pooled analysis

  • Asia-Pacific Cohort Studies Collaboration (APCSC)
  • , Diabetes Epidemiology Collaborative Analysis Of Diagnostic Criteria In Europe (DECODE)
  • , Prospective Studies Collaboration (PSC)
  • , Global Burden Of Metabolic Risk Factors Of Chronic Diseases Collaborating Group
  • , Emerging Risk Factor Collaboration (ERFC)
  • Harvard University
  • Tehran University of Medical Sciences
  • World Health Organization
  • The University of Sydney
  • Johns Hopkins University
  • University of Cambridge
  • University of Oxford
  • University of Helsinki
  • University of Melbourne
  • The University of Auckland
  • Emory University
  • Brigham and Women’s Hospital
  • Medical Research Council
  • Glostrups Study
  • East-West Study
  • National FINRISK 1987 and 1992 Cohorts
  • National FINRISK 2002 Study
  • Vantaa Study
  • Helsinki Policemen Study
  • Oulu Study
  • Cremona Study
  • University of Oulu
  • Malmo Preventive Project
  • Northern Sweden MONICA Survey
  • The Uppsala Longitudinal Study of Adult Men (ULSAM)
  • The Hoorn Study
  • Zutphen Study
  • Isle of Ely Diabetes Project

Research output: Contribution to journalArticlepeer-review

661 Scopus citations

Abstract

Background: The effects of systolic blood pressure (SBP), serum total cholesterol (TC), fasting plasma glucose (FPG), and body mass index (BMI) on the risk of cardiovascular diseases (CVD) have been established in epidemiological studies, but consistent estimates of effect sizes by age and sex are not available. Methods: We reviewed large cohort pooling projects, evaluating effects of baseline or usual exposure to metabolic risks on ischemic heart disease (IHD), hypertensive heart disease (HHD), stroke, diabetes, and, as relevant selected other CVDs, after adjusting for important confounders. We pooled all data to estimate relative risks (RRs) for each risk factor and examined effect modification by age or other factors, using random effects models. Results: Across all risk factors, an average of 123 cohorts provided data on 1.4 million individuals and 52,000 CVD events. Each metabolic risk factor was robustly related to CVD. At the baseline age of 55-64 years, the RR for 10 mmHg higher SBP was largest for HHD (2.16; 95% CI 2.09-2.24), followed by effects on both stroke subtypes (1.66; 1.39-1.98 for hemorrhagic stroke and 1.63; 1.57-1.69 for ischemic stroke). In the same age group, RRs for 1 mmol/L higher TC were 1.44 (1.29-1.61) for IHD and 1.20 (1.15-1.25) for ischemic stroke. The RRs for 5 kg/m2 higher BMI for ages 55-64 ranged from 2.32 (2.04-2.63) for diabetes, to 1.44 (1.40-1.48) for IHD. For 1 mmol/L higher FPG, RRs in this age group were 1.18 (1.08-1.29) for IHD and 1.14 (1.01-1.29) for total stroke. For all risk factors, proportional effects declined with age, were generally consistent by sex, and differed by region in only a few age groups for certain risk factor-disease pairs. Conclusion: Our results provide robust, comparable and precise estimates of the effects of major metabolic risk factors on CVD and diabetes by age group.

Original languageEnglish
Article numbere65174
JournalPLOS ONE
Volume8
Issue number7
DOIs
StatePublished - Jul 30 2013

Fingerprint

Dive into the research topics of 'The age-specific quantitative effects of metabolic risk factors on cardiovascular diseases and diabetes: A pooled analysis'. Together they form a unique fingerprint.

Cite this