Competing Risks of Coronary Heart Disease Mortality versus Other Causes of Death in 10 Cohorts of Middle-Aged Men of the Seven Countries Study Followed for 60 Years to Extinction

Author:

Puddu Paolo Emilio12ORCID,Piras Paolo3ORCID,Kafatos Anthony4,Adachi Hisashi5ORCID,Tolonen Hanna6ORCID,Menotti Alessandro1ORCID

Affiliation:

1. Association for Cardiac Research, 00182 Rome, Italy

2. EA 4650, Signalisation, Électrophysiologie et Imagerie des Lésions d’Ischémie Reperfusion Myocardique, Université de Normandie, 14032 Caen, France

3. Department of Structural Engineering, Sapienza University of Rome, 00185 Rome, Italy

4. Department of Social Medicine, Preventive Medicine and Nutrition Clinic, University of Crete, 70013 Heraklion, Greece

5. Department of Internal Medicine, Division of Cardio-Vascular Medicine, School of Medicine, Kurume University, Kurume 830-0011, Japan

6. Department of Public Health and Welfare, Finnish Institute for Health and Welfare, FI-00271 Helsinki, Finland

Abstract

Objectives: To assess whether competing risks help explain why regions with initially high serum cholesterol have higher mortality from coronary heart disease (CHD) and lower mortality from stroke and other major heart diseases, while the reverse is found for those with initially lower serum cholesterol. Material and Methods. Ten cohorts of men (N = 9063) initially aged 40–59 in six countries were examined and followed for fatal outcomes for 60 years. Major cardiovascular disease (CVD) groups were CHD, stroke, and other Heart Diseases of Uncertain Etiology (HDUE), or the combination of stroke and HDUE (STHD), along with all other causes of death. Fine-Gray competing risk analysis was applied with CHD versus all other causes of death or STHD (direct mode) and all other causes of death or STHD versus CHD (inverse mode), and the effects of 19 covariates (of which 3 references) on the cause-specific hazard of the outcomes were assessed, thus investigating potential etiologic roles. A systematic comparison with results obtained by running the Cox model in direct and inverse modes with the same end-point results was also performed and illustrated graphically. Results. CHD mortality is bound to different risk factor relationships when compared with all other causes of death and with STHD. The role of serum cholesterol is crucial since, in both comparisons, by Fine-Gray, its coefficients are positive and significant for CHD and negative and significant for all other causes of death and STHD. Risk factor capabilities in specific outcome types of the CVD domain (CHD versus STHD) are different depending on the outcome types considered. Risk factor coefficients are smaller in Fine-Gray modelling and larger in the Cox model. Fine-Gray detects different risk factors whose coefficients may have opposite algebraic signs. Conclusions. This is the first report whereby a large group of risk factors are investigated in connection with life-long CVD outcomes by Fine-Gray competing risk analysis, and a systematic comparison is performed with results obtained by Cox models in both direct and inverse modes. Subtypes of CVD mortality should be summed with full awareness that some risk factors vary by pathology, and they should at least be disentangled into CHD and STHD.

Publisher

MDPI AG

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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