Effects of a Vegetarian Diet on Cardiometabolic Risk Factors, Gut Microbiota, and Plasma Metabolome in Subjects With Ischemic Heart Disease: A Randomized, Crossover Study

Author:

Djekic Demir1ORCID,Shi Lin23,Brolin Harald4,Carlsson Frida3,Särnqvist Charlotte1,Savolainen Otto3,Cao Yang5ORCID,Bäckhed Fredrik467,Tremaroli Valentina4,Landberg Rikard38,Frøbert Ole1

Affiliation:

1. Department of Cardiology, Faculty of Health Örebro University Hospital Örebro Sweden

2. Engineering and Nutritional Science Shaanxi Normal University Xi’an China

3. Chalmers University of Technology Gothenburg Sweden

4. The Wallenberg Laboratory, Department of Molecular and Clinical Medicine University of Gothenburg Sweden

5. Clinical Epidemiology and Biostatistics, School of Medical Sciences Örebro University Örebro Sweden

6. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences University of Copenhagen Denmark

7. Department of Clinical Physiology, Region Västra Götaland Sahlgrenska University Hospital Gothenburg Sweden

8. Department of Public Health and Clinical Medicine Umeå University Umeå Sweden

Abstract

Background A vegetarian diet (VD) may reduce future cardiovascular risk in patients with ischemic heart disease. Methods and Results A randomized crossover study was conducted in subjects with ischemic heart disease, assigned to 4‐week intervention periods of isocaloric VD and meat diet (MD) with individually designed diet plans, separated by a 4‐week washout period. The primary outcome was difference in oxidized low‐density lipoprotein cholesterol (LDL‐C) between diets. Secondary outcomes were differences in cardiometabolic risk factors, quality of life, gut microbiota, fecal short‐chain and branched‐chain fatty acids, and plasma metabolome. Of 150 eligible patients, 31 (21%) agreed to participate, and 27 (87%) participants completed the study. Mean oxidized LDL‐C (−2.73 U/L), total cholesterol (−5.03 mg/dL), LDL‐C (−3.87 mg/dL), and body weight (−0.67 kg) were significantly lower with the VD than with the MD. Differences between VD and MD were observed in the relative abundance of several microbe genera within the families Ruminococcaceae, Lachnospiraceae, and Akkermansiaceae. Plasma metabolites, including l ‐carnitine, acylcarnitine metabolites, and phospholipids, differed in subjects consuming VD and MD. The effect on oxidized LDL‐C in response to the VD was associated with a baseline gut microbiota composition dominated by several genera of Ruminococcaceae. Conclusions The VD in conjunction with optimal medical therapy reduced levels of oxidized LDL‐C, improved cardiometabolic risk factors, and altered the relative abundance of gut microbes and plasma metabolites in patients with ischemic heart disease. Our results suggest that composition of the gut microbiota at baseline may be related to the reduction of oxidized LDL‐C observed with the VD. Registration URL: https://www.clini​caltr​ials.gov ; Unique identifier: NCT02942628.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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