Literature DB >> 30473327

Relation of Alcohol Consumption to Left Ventricular Fibrosis Using Cardiac Magnetic Resonance Imaging.

Aleksandr Voskoboinik1, Benedict T Costello2, Andre La Gerche3, Sandeep Prabhu1, Geoff Wong4, Michael D Flannery3, Chrishan Nalliah5, Hariharan Sugumar1, Fabian Springer6, Jonathan M Kalman7, Andrew J Taylor2, Peter M Kistler8.   

Abstract

Light-to-moderate regular alcohol consumption has been associated with reduced mortality, heart failure, and sudden death, with a well described "U-shaped" relationship. We sought to determine whether markers of diffuse ventricular fibrosis as assessed by cardiac magnetic resonance imaging (CMR) T1 mapping differ between nondrinkers and regular drinkers. We prospectively recruited 165 participants to undergo 3T CMR ventricular T1 mapping which included 120 regular light-to-moderate drinkers (7 to 28 standard drinks per week for >12 months) and 45 age and gender-matched nondrinking controls (1 standard drink ∼12 g alcohol). Diffuse ventricular fibrosis was assessed using ShMOLLI T1 mapping sequences performed in mid-short axis. Native T1, postcontrast T1 times and extracellular volume were compared in the left ventricle between regular drinkers and lifelong nondrinkers. In total 165 participants (mean age 59 ± 12 years, 70% male, 36% hypertension, mean LVEF 58 ± 11%) underwent CMR. Moderate alcohol intake (mean alcohol intake 16 ± 6 SDs/week) was associated with lower markers of diffuse ventricular fibrosis: native T1 time 1140 ± 47 vs 1173 ± 39 ms, p < 0.001; postcontrast T1 time 470 ± 47 vs 445 ± 43 ms, p = 0.01; extracellular volume 25.0 ± 2.7% vs 27.0 ± 2.8%, p = 0.003 despite similar LV size (p = 0.55) and mass compared with nondrinkers (p = 0.78). Quantity of alcohol intake and beverage type did not predict lower native T1 times. In conclusion, light-to-moderate or "social" alcohol consumption is associated with T1 changes on CMR suggestive of a reduction in diffuse ventricular fibrosis. These preliminary findings may provide some insights into the association between modest alcohol intake and reduction in sudden death and heart failure.
Copyright © 2018. Published by Elsevier Inc.

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Year:  2018        PMID: 30473327     DOI: 10.1016/j.amjcard.2018.10.026

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  4 in total

1.  Alcohol consumption in the general population is associated with structural changes in multiple organ systems.

Authors:  Hideaki Suzuki; Wenjia Bai; Evangelos Evangelou; Raha Pazoki; He Gao; Paul M Matthews; Paul Elliott
Journal:  Elife       Date:  2021-06-01       Impact factor: 8.713

2.  Sex-specific associations between alcohol consumption, cardiac morphology, and function as assessed by magnetic resonance imaging: insights form the UK Biobank Population Study.

Authors:  Judit Simon; Kenneth Fung; Márton Kolossváry; Mihir M Sanghvi; Nay Aung; Jose Miguel Paiva; Elena Lukaschuk; Valentina Carapella; Béla Merkely; Marcio S Bittencourt; Júlia Karády; Aaron M Lee; Stefan K Piechnik; Stefan Neubauer; Pál Maurovich-Horvat; Steffen E Petersen
Journal:  Eur Heart J Cardiovasc Imaging       Date:  2021-08-14       Impact factor: 9.130

Review 3.  Therapeutic Targets for the Treatment of Cardiac Fibrosis and Cancer: Focusing on TGF-β Signaling.

Authors:  Warisara Parichatikanond; Theerut Luangmonkong; Supachoke Mangmool; Hitoshi Kurose
Journal:  Front Cardiovasc Med       Date:  2020-03-10

4.  Moderate excess alcohol consumption and adverse cardiac remodelling in dilated cardiomyopathy.

Authors:  Upasana Tayal; John Gregson; Rachel Buchan; Nicola Whiffin; Brian P Halliday; Amrit Lota; Angharad M Roberts; A John Baksi; Inga Voges; Julian W E Jarman; Resham Baruah; Michael Frenneaux; John G F Cleland; Paul Barton; Dudley J Pennell; James S Ware; Stuart A Cook; Sanjay K Prasad
Journal:  Heart       Date:  2021-08-11       Impact factor: 5.994

  4 in total

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