Essential Amino Acid Supplement Lowers Intrahepatic Lipid despite Excess Alcohol Consumption.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
19 Jan 2020
Historique:
received: 16 12 2019
revised: 07 01 2020
accepted: 09 01 2020
entrez: 23 1 2020
pubmed: 23 1 2020
medline: 20 11 2020
Statut: epublish

Résumé

Excess alcohol consumption is a top risk factor for death and disability. Fatty liver will likely develop and the risk of liver disease increases. We have previously demonstrated that an essential amino acid supplement (EAAS) improved protein synthesis and reduced intrahepatic lipid in the elderly. The purpose of this exploratory pilot study was to initiate the evaluation of EAAS on intrahepatic lipid (IHL), body composition, and blood lipids in individuals with mild to moderate alcohol use disorder (AUD). Following consent, determination of eligibility, and medical screening, 25 participants (18 males at 38 ± 15 years/age and 7 females at 34 ± 18 years/age) were enrolled and randomly assigned to one of two dosages: a low dose (LD: 8 g of EAAS twice/day (BID)) or high dose (HD: 13 g of EAAS BID). Five of the twenty-five enrolled participants dropped out of the intervention. Both groups consumed the supplement BID for 4 weeks. Pre- and post-EAAS administration, IHL was determined using magnetic resonance imaging/spectroscopy, body composition was analyzed using dual-energy X-ray absorptiometry, and blood parameters were measured by LabCorp. T-tests were used for statistical analysis and considered significant at

Identifiants

pubmed: 31963802
pii: nu12010254
doi: 10.3390/nu12010254
pmc: PMC7019240
pii:
doi:

Substances chimiques

Amino Acids, Essential 0
Biomarkers 0
Lipids 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : TL4 GM118992
Pays : United States
Organisme : NIGMS NIH HHS
ID : UL1 GM118991
Pays : United States
Organisme : NIGMS NIH HHS
ID : RL5 GM118990
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM130443
Pays : United States
Organisme : NIH HHS
ID : P20GM103395
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM103395
Pays : United States
Organisme : NIGMS NIH HHS
ID : T34 GM141009
Pays : United States
Organisme : NIH HHS
ID : UL1GM118991
Pays : United States

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Auteurs

Melynda S Coker (MS)

Department of Natural Resources and Environment, University of Alaska Fairbanks, 505 South Chandalar Drive, Fairbanks, AK 99775, USA.

Kaylee R Ladd (KR)

Department of Biology and Wildlife, University of Alaska Fairbanks, Fairbanks, AK 99775, USA.

Jimin Kim (J)

Department of Biology and Wildlife, University of Alaska Fairbanks, Fairbanks, AK 99775, USA.

Carl J Murphy (CJ)

Institute of Arctic Biology, Department of Chemistry & Biochemistry, University of Alaska Fairbanks1930 Yukon Dr. Room 136, Fairbanks, AK 99775, USA.

Ryan DeCort (R)

Bassett Army Community Hospital, 4076 Neely Road, FortWainwright, United States Army, Fairbanks, AK 99703, USA.

Bradley R Newcomer (BR)

Honors College, 1501 251Warren Service Drive, Room 105, James Madison University, Harrisonburg, VA 22807, USA.

Robert R Wolfe (RR)

Department of Geriatrics, Center for Translational Research in Aging & Longevity, Donald W. Reynolds Institute on Aging, 4301 West Markham, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.

Robert H Coker (RH)

Department of Biology and Wildlife, University of Alaska Fairbanks, Fairbanks, AK 99775, USA.
Institute of Arctic Biology, Department of Chemistry & Biochemistry, University of Alaska Fairbanks1930 Yukon Dr. Room 136, Fairbanks, AK 99775, USA.

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