Display options
Share it on

World J Hepatol. 2017 Jul 08;9(19):857-866. doi: 10.4254/wjh.v9.i19.857.

Is hepatic steatosis associated with left ventricular mass index increase in the general population?.

World journal of hepatology

Katharina Piontek, Carsten O Schmidt, Sebastian E Baumeister, Markus M Lerch, Julia Mayerle, Marcus Dörr, Stephan B Felix, Henry Völzke

Affiliations

  1. Katharina Piontek, Institute for Medical Psychology, University Medicine Greifswald, 17489 Greifswald, Germany.

PMID: 28740597 PMCID: PMC5504361 DOI: 10.4254/wjh.v9.i19.857

Abstract

AIM: To investigate the association between hepatic steatosis and change in left ventricular mass index (LVMI) over five years, and examine whether systolic and diastolic blood pressures are mediators of the association between hepatic steatosis and LVMI using a general population sample.

METHODS: We analyzed data from the Study of Health in Pomerania. The study population comprised 1298 individuals aged 45 to 81 years. Hepatic steatosis was defined as the presence of a hyperechogenic pattern of the liver together with elevated serum alanine transferase levels. Left ventricular mass was determined echocardiographically and indexed to height

RESULTS: Hepatic steatosis was a significant predictor for all measured echocardiographic characteristics at baseline. Path analyses revealed that the association of hepatic steatosis with LVMI change after five years was negligibly small (β = -0.12, s.e. = 0.21,

CONCLUSION: Baseline associations between hepatic steatosis and LVMI do not extend to associations with LVMI change after five years. More studies are needed to study the longitudinal effects of hepatic steatosis on LVMI.

Keywords: Blood pressure; General Population; Hepatic steatosis; Left ventricular mass index; Study of Health in Pomerania

Conflict of interest statement

Conflict-of-interest statement: The authors declare that they have no conflicts of interest.

References

  1. Eur Heart J. 1999 Mar;20(6):429-38 - PubMed
  2. Ann Intern Med. 1969 Jul;71(1):89-105 - PubMed
  3. Int J Epidemiol. 2011 Apr;40(2):294-307 - PubMed
  4. J Clin Epidemiol. 2009 Mar;62(3):252-60 - PubMed
  5. Br J Clin Pharmacol. 1999 Feb;47(2):125-30 - PubMed
  6. Am J Hypertens. 2008 Apr;21(4):458-63 - PubMed
  7. Diabetes Care. 2008 Aug;31(8):1629-34 - PubMed
  8. Nutr Metab Cardiovasc Dis. 2009 Nov;19(9):646-53 - PubMed
  9. Eur J Cardiovasc Prev Rehabil. 2009 Jun;16(3):392-400 - PubMed
  10. N Engl J Med. 1990 May 31;322(22):1561-6 - PubMed
  11. Am J Cardiol. 1986 Feb 15;57(6):450-8 - PubMed
  12. J Am Soc Echocardiogr. 2005 Dec;18(12 ):1440-63 - PubMed
  13. Gastroenterology. 2008 Jan;134(1):85-94 - PubMed
  14. Gut. 2004 Jul;53(7):1020-3 - PubMed
  15. J Hepatol. 2001 Oct;35(4):531-7 - PubMed
  16. Gut. 2007 Apr;56(4):594-5 - PubMed
  17. Ann Intern Med. 1988 Jan;108(1):7-13 - PubMed
  18. J Hypertens. 2011 Jan;29(1):17-26 - PubMed
  19. J Hum Hypertens. 2004 Dec;18 Suppl 2:S23-8 - PubMed
  20. Gesundheitswesen. 2000 Apr;62(4):234-43 - PubMed
  21. Clin Endocrinol (Oxf). 1999 Jun;50(6):703-13 - PubMed
  22. Am Heart J. 1987 Oct;114(4 Pt 2):975-83 - PubMed
  23. J Endocrinol Invest. 2012 Feb;35(2):215-8 - PubMed
  24. J Clin Epidemiol. 2011 Apr;64(4):416-23 - PubMed
  25. Diabetes Care. 2012 Feb;35(2):389-95 - PubMed
  26. Curr Hypertens Rep. 2015 Oct;17 (10 ):77 - PubMed
  27. World J Gastroenterol. 2005 Mar 28;11(12):1848-53 - PubMed
  28. J Hypertens. 1998 Jun;16(6):715-23 - PubMed
  29. J Hypertens. 2002 Feb;20(2):323-31 - PubMed
  30. J Clin Gastroenterol. 2006 Nov-Dec;40(10 ):949-55 - PubMed
  31. J Hypertens. 2010 May;28(5):1065-73 - PubMed

Publication Types