Cited by 202Diabetes, Cardiovascular Risks, and LipoproteinsCardiovascular Function and Risk FactorsAdipokines, Inflammation, and Metabolic Diseases

The progression of cardiometabolic disease: validation of a new cardiometabolic disease staging system applicable to obesity

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Guo, Fangjian, Moellering, Douglas R., Garvey, W. Timothy·2014·Obesity

Abstract

Objective: To validate a Cardiometabolic Disease Staging (CMDS) system for assigning risk level for diabetes, and all‐cause and cardiovascular disease (CVD) mortality. Design and Methods: Two large national cohorts, CARDIA and NHANES III, were used to validate CMDS. CMDS: Stage 0: metabolically healthy; Stage 1: one or two metabolic syndrome risk factors [other than impaired fasting glucose (IFG)]; Stage 2: IFG or impaired glucose tolerance (IGT) or metabolic syndrome (without IFG); Stage 3: two of three (IFG, IGT, and/or metabolic syndrome); and Stage 4: type 2 diabetes mellitus/CVD. Results: In the CARDIA study, compared with Stage 0 metabolically healthy subjects, adjusted risk for diabetes exponentially increased from Stage 1 [hazard ratio (HR) 2.83, 95% confidence interval (CI): 1.76‐4.55], to Stage 2 (HR 8.06, 95% CI 4.91‐13.2), to Stage 3 (HR 23.5, 95% CI 13.7‐40.1) ( P for trend <0.001). In NHANES III, both cumulative incidence and multivariable adjusted HRs markedly increased for both all‐cause and CVD mortality with advancement of the risk stage from Stages 0 to 4. Adjustment for body mass index (BMI) minimally affected the risks for diabetes and all‐cause/CVD mortality using CMDS. Conclusion: CMDS can discriminate a wide range of risk for diabetes, CVD mortality, and all‐cause mortality independent of BMI, and should be studied as a risk assessment tool to guide interventions that prevent and treat cardiometabolic disease.

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References 47 · Cited by 202

Authors
Guo, F., Moellering, D. R., & Garvey, W. T.
Affiliations
University of Alabama at Birmingham (US)
Corresponding author
  • Guo, Fangjian
  • Garvey, W. Timothy
Venue
Obesity
Publisher
Wiley
Published
2013-09-05
Volume
22
Issue
1
Pages
110-118
ISSN
  • 1930-7381 (ISSN-L)
  • 1930-739X
OpenAlex
W1535711205
Cited by
202
References
47
Citations by year
2026: 12 · 2025: 18 · 2024: 22 · 2023: 25 · 2022: 22 · 2021: 19 · 2020: 12 · 2019: 11 · 2018: 20 · 2017: 19 · 2016: 10 · 2015: 6 · 2014: 5 · 2013: 1
FWCI
5.77
Type
journal article
Language
en
Open access
Locations
  • Obesity (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • U.S. Department of Veterans Affairs (I01CX000432)
  • National Institutes of Health (5p60dk079626-05)
  • National Institute of Diabetes and Digestive and Kidney Diseases (P60-DK-079626, R01DK038765, DK038765, DK-083562, R01DK083562, P30DK079626)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
Keywords
metabolic syndrome, type 2 diabetes risk, cardiovascular mortality, all-cause mortality, impaired fasting glucose, impaired glucose tolerance, body mass index, risk stratification, disease progression
MeSH terms
Adolescent, Adult, Blood Glucose, Cardiovascular Diseases, Cross-Sectional Studies, Diabetes Mellitus, Type 2, Female, Humans, Longitudinal Studies, Male, Nutrition Surveys, Obesity, Risk Factors, Cohort Studies, Body Mass Index, Incidence, Proportional Hazards Models, Randomized Controlled Trials as Topic, Glucose Intolerance, Disease Progression, Risk Assessment, Metabolic Syndrome, Young Adult

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