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Dilated cardiomyopathy risk factors

Introduction

Overview

Overview

Common risk factors in the development of dilated cardiomyopathy include genetic inheritance, nutritional deficiencies, substance abuse, occupational exposure to toxins, and viral infections.

Risk Factors

Risk Factors

Common risk factors in the development of dilated cardiomyopathy include genetic inheritance, nutritional deficiencies, substance abuse, occupational exposure to toxins, and viral infections.[1][2][3][4]

Common Risk Factors

Less Common Risk Factors

References

References

  1. ↑ Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL; et al. (2000). “Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy”. N Engl J Med. 342 (15): 1077–84. doi:10.1056/NEJM200004133421502. PMID 10760308.
  2. ↑ McNally EM, Mestroni L (2017). “Dilated Cardiomyopathy: Genetic Determinants and Mechanisms”. Circ Res. 121 (7): 731–748. doi:10.1161/CIRCRESAHA.116.309396. PMC 5626020. PMID 28912180.
  3. ↑ Lipshultz SE (1998). “Dilated cardiomyopathy in HIV-infected patients”. N Engl J Med. 339 (16): 1153–5. doi:10.1056/NEJM199810153391609. PMID 9770563.
  4. ↑ Li X, Nie Y, Lian H, Hu S (2018). “Histopathologic features of alcoholic cardiomyopathy compared with idiopathic dilated cardiomyopathy”. Medicine (Baltimore). 97 (39): e12259. doi:10.1097/MD.0000000000012259. PMC 6181549. PMID 30278496.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdelrahman Ibrahim Abushouk, MD[2]