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Associations of Concurrent Hypertension and Type 2 Diabetes with Mortality Outcomes: A Prospective Study of US Adults

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Version 2 2025-05-22, 19:33
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posted on 2025-05-22, 19:33 authored by Ye Yuan, Carmen R. Isasi, Tala Al-Rousan, Arnab K. Ghosh, Pricila H. Mullachery, Priya Palta, Nour Makarem

Objective: To investigate associations of concurrent hypertension and type 2 diabetes(T2D) with mortality in US adults and elucidate differences by sex, race, and ethnicity. Research Design and Methods: The study population included 48,727 adults from the 1999-2018 National Health and Nutrition Examination Surveys(NHANES). Participants were categorized into 4 mutually exclusive categories: 1) no hypertension and no T2D, 2) hypertension only, 3) T2D only, and 4) co-existing hypertension and T2D. Outcomes were all-cause and cardiovascular mortality, defined using ICD-10 codes. Kaplan-Meier curves and multivariable Cox proportional hazards models were used to evaluate associations of hypertension and T2D status with mortality risk. Results: The burden of concurrent hypertension and T2D doubled between1999-2018 from 6% to 12%. Overall, 50.5% did not have T2D or hypertension, 38.4% had hypertension only, 2.4% had T2D only, and 8.7% had both. During a 9.2y median follow-up, 7,734 deaths occurred. Concurrent hypertension and T2D vs. no hypertension or T2D predicted higher all-cause(HR(95%CI):2.46(2.45-2.47)) and cardiovascular mortality risk(HR(95%CI):2.97(2.94-3.00)), with stronger associations in females vs. males(p-interaction<0.01). Compared to having hypertension or T2D only, concurrent hypertension and T2D predicted up to 66% and >2-fold higher all-cause and cardiovascular mortality risk, respectively, and associations varied by sex, race, and ethnicity (p-interaction<0.01) depending on the referent group (T2D only or hypertension only). Concurrent prediabetes and elevated blood pressure predicted up to 19% higher mortality risk compared to having neither or either condition. Conclusions: Concurrent hypertension and T2D predict high mortality risk underscoring the critical need for contextual interventions that extend healthspan in the US.

Funding

Dr. Makarem is supported by NHLBI Grant # R00-HL148511, American Heart Association Grant #855050, NIMHD Grants # P50MD017341 (sub-project ID: 8126) and P50MD017341-03S2, and American Heart Association Grant #24FIM1267661. Dr. Al-Rousan is supported by NHLBI Grant # K23-HL148530, and NIA Grant #2P30AG059299. Dr. Ghosh is supported by NHBLI grant #K08HL163329. Drs. Makarem and Isasi were also supported by the New York Regional Center for Diabetes Translation Research (P30 DK111022). The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

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