Association of Cardiometabolic Multimorbidity With Mortality

Emanuele Di Angelantonio(University of Cambridge), Stephen Kaptoge(University of Cambridge), David Wormser(University of Cambridge), Peter Willeit(University of Cambridge), Adam S. Butterworth(University of Cambridge), Narinder Bansal(University of Cambridge), Linda M. O’Keeffe(University of Cambridge), Pei Gao(University of Cambridge), Angela Wood(University of Cambridge), Stephen Burgess(University of Cambridge), Daniel F. Freitag(University of Cambridge), Lisa Pennells(University of Cambridge), Sanne A. E. Peters(University Medical Center Utrecht), Carole Hart(University of Glasgow), Lise Lund Håheim(University of Oslo), Richard F. Gillum(Howard University), Børge G. Nordestgaard(University of Copenhagen), Bruce M. Psaty(University of Washington), Bu B. Yeap(The University of Western Australia), Matthew Knuiman(The University of Western Australia), Paul J. Nietert(Medical University of South Carolina), Jussi Kauhanen(University of Eastern Finland), Jukka T. Salonen, Lewis H. Kuller(University of Pittsburgh), Leon A. Simons(UNSW Sydney), Yvonne T. van der Schouw(University Medical Center Utrecht), Elizabeth Barrett‐Connor(University of California San Diego), Randi Selmer(Norwegian Institute of Public Health), Carlos J. Crespo(Portland State University), Beatriz L. Rodríguez(University of Hawaii System), W. M. Monique Verschuren(National Institute for Public Health and the Environment), Veikko Salomaa(Finnish Institute for Health and Welfare), Kurt Svärdsudd(Uppsala University), Pim van der Harst(University Medical Center Groningen), Cecilia Björkelund(University of Gothenburg), Lars Wilhelmsen(University of Gothenburg), Robert B. Wallace(University of Iowa), Hermann Brenner(German Cancer Research Center), Philippe Amouyel(Institut Pasteur de Lille), Elizabeth Barr(Baker Heart and Diabetes Institute), Hiroyasu Iso(The University of Osaka), Altan Onat(Istanbul University), Maurizio Trevisan(City College of New York), Ralph B. D’Agostino, Cyrus Cooper(University of Southampton), Maryam Kavousi(Erasmus MC), Lennart Welin(Sjukhuset i Lidköping), Ronan Roussel(Université Paris Cité), Frank B. Hu(Harvard University), Shinichi Sato(Chiba Prefectural Institute of Public Health), Karina W. Davidson(Columbia University Irving Medical Center), Barbara V. Howard(MedStar Health), Maarten J.G. Leening(Erasmus MC), Annika Rosengren(University of Gothenburg), Marcus Dörr(Universitätsmedizin Greifswald), Dorly J. H. Deeg(Vrije Universiteit Amsterdam), Stefan Kiechl(Innsbruck Medical University), Coen D.A. Stehouwer(Maastricht University Medical Centre), Aulikki Nissinen(Finnish Institute for Health and Welfare), Simona Giampaoli(Istituto Superiore di Sanità), Chiara Donfrancesco(Istituto Superiore di Sanità), Daan Kromhout(Wageningen University & Research), Jackie F. Price(University of Edinburgh), Annette Peters(Helmholtz Zentrum München), Tom Meade(London School of Hygiene & Tropical Medicine), Edoardo Casiglia(University of Padua), Debbie A. Lawlor(University of Bristol), John Gallacher(Cardiff University), Dorothea Nagel(LMU Klinikum), Oscar H. Franco(Erasmus MC), Gerd Assmann(Homann-Stiftung), Gilles R. Dagenais(Institut universitaire de cardiologie et de pneumologie de Québec), J. Wouter Jukema(Leiden University Medical Center), Johan Sundström(Uppsala University), Mark Woodward(The University of Sydney), Eric J. Brunner(University College London), Kay-Tee Khaw(University of Cambridge), Nicholas J. Wareham(Medical Research Council), Eric A. Whitsel(University of North Carolina at Chapel Hill), Inger Njølstad(UiT The Arctic University of Norway), Bo Hedblad(Lund University), Sylvia Wassertheil‐Smoller(Albert Einstein College of Medicine), Gunnar Engström(Lund University), Wayne D. Rosamond(University of North Carolina at Chapel Hill), Elizabeth Selvin(Johns Hopkins University), Naveed Sattar(University of Glasgow), Simon G. Thompson(University of Cambridge), John Danesh(University of Cambridge)
JAMA
July 7, 2015
Cited by 1,110Open Access
Full Text

Abstract

IMPORTANCE: The prevalence of cardiometabolic multimorbidity is increasing. OBJECTIVE: To estimate reductions in life expectancy associated with cardiometabolic multimorbidity. DESIGN, SETTING, AND PARTICIPANTS: Age- and sex-adjusted mortality rates and hazard ratios (HRs) were calculated using individual participant data from the Emerging Risk Factors Collaboration (689,300 participants; 91 cohorts; years of baseline surveys: 1960-2007; latest mortality follow-up: April 2013; 128,843 deaths). The HRs from the Emerging Risk Factors Collaboration were compared with those from the UK Biobank (499,808 participants; years of baseline surveys: 2006-2010; latest mortality follow-up: November 2013; 7995 deaths). Cumulative survival was estimated by applying calculated age-specific HRs for mortality to contemporary US age-specific death rates. EXPOSURES: A history of 2 or more of the following: diabetes mellitus, stroke, myocardial infarction (MI). MAIN OUTCOMES AND MEASURES: All-cause mortality and estimated reductions in life expectancy. RESULTS: In participants in the Emerging Risk Factors Collaboration without a history of diabetes, stroke, or MI at baseline (reference group), the all-cause mortality rate adjusted to the age of 60 years was 6.8 per 1000 person-years. Mortality rates per 1000 person-years were 15.6 in participants with a history of diabetes, 16.1 in those with stroke, 16.8 in those with MI, 32.0 in those with both diabetes and MI, 32.5 in those with both diabetes and stroke, 32.8 in those with both stroke and MI, and 59.5 in those with diabetes, stroke, and MI. Compared with the reference group, the HRs for all-cause mortality were 1.9 (95% CI, 1.8-2.0) in participants with a history of diabetes, 2.1 (95% CI, 2.0-2.2) in those with stroke, 2.0 (95% CI, 1.9-2.2) in those with MI, 3.7 (95% CI, 3.3-4.1) in those with both diabetes and MI, 3.8 (95% CI, 3.5-4.2) in those with both diabetes and stroke, 3.5 (95% CI, 3.1-4.0) in those with both stroke and MI, and 6.9 (95% CI, 5.7-8.3) in those with diabetes, stroke, and MI. The HRs from the Emerging Risk Factors Collaboration were similar to those from the more recently recruited UK Biobank. The HRs were little changed after further adjustment for markers of established intermediate pathways (eg, levels of lipids and blood pressure) and lifestyle factors (eg, smoking, diet). At the age of 60 years, a history of any 2 of these conditions was associated with 12 years of reduced life expectancy and a history of all 3 of these conditions was associated with 15 years of reduced life expectancy. CONCLUSIONS AND RELEVANCE: Mortality associated with a history of diabetes, stroke, or MI was similar for each condition. Because any combination of these conditions was associated with multiplicative mortality risk, life expectancy was substantially lower in people with multimorbidity.


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