Evidence map›Paper›PMID 29960116›Full record

ArticleThe Journal of nutritional biochemistry2018

Association of serum zinc with markers of liver injury in very heavy drinking alcohol-dependent patients.

Vatsalya Vatsalya, Maiying Kong, Matthew C Cave, Nanlong Liu, Melanie L Schwandt, David T George, Vijay A Ramchandani, Craig J McClain

Abstract read
In one paragraph

Article in The Journal of nutritional biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 40 citations in OpenAlex.

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  16. Article
  17. Dysregulation in PlasmaAdvances in virology · 2020
    Article
  18. Microbiome dysbiosis and alcoholic liver diseaseLiver research (Beijing, China) · 2019
    Article
  19. Hepatology communications · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Vatsalya VatsalyaDivision of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Louisville, Louisville, KY; Section on Human Psychopharmacology, LCTS DICBR NIAAA National Institutes of Health, Bethesda, MD; Robley Rex Veterans Medical Center, Louisville, KY; University of Louisville Alcohol Research Center, Louisville, KY; Hepatobiology & Toxicology COBRE, University of Louisville, Louisville, KY. Electronic address: v0vats01@exchange.louisville.edu.
Maiying KongDepartment of Biostatistics and Bioinformatics, School of Public Health and Information Sciences, University of Louisville, Louisville, KY.
Matthew C CaveDivision of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Louisville, Louisville, KY; Robley Rex Veterans Medical Center, Louisville, KY; University of Louisville Alcohol Research Center, Louisville, KY; Hepatobiology & Toxicology COBRE, University of Louisville, Louisville, KY; Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY.
Nanlong LiuDivision of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Louisville, Louisville, KY.
Melanie L SchwandtOffice of Clinical Director, NIAAA National Institutes of Health, Bethesda, MD.
David T GeorgeOffice of Clinical Director, NIAAA National Institutes of Health, Bethesda, MD.
Vijay A RamchandaniSection on Human Psychopharmacology, LCTS DICBR NIAAA National Institutes of Health, Bethesda, MD.
Craig J McClainDivision of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Louisville, Louisville, KY; Robley Rex Veterans Medical Center, Louisville, KY; University of Louisville Alcohol Research Center, Louisville, KY; Hepatobiology & Toxicology COBRE, University of Louisville, Louisville, KY; Department of Biostatistics and Bioinformatics, School of Public Health and Information Sciences, University of Louisville, Louisville, KY; Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY.
National Institutes of Health · USUniversity of Louisville · US

Funding

NIAAA Repository/Screening Database Management and ResearchZIAAA000130 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI SCHWANDT, MELANIE · 2017 to 2025
$60.1M
Alcohol Pharmacokinetics and Pharmacodynamics in HumansZIAAA000466 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI RAMCHANDANI, VIJAY ARJUN · 2009 to 2025
$31.2M
Role of oxidized linoleic acid metabolites in the pathogenesis of alcoholic liver diseaseP20GM113226 · NIGMS · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2016 to 2025
$24.1M
The Role of Nutrition in the Development/Progression of Alcohol-Induced Organ InjuryP50AA024337 · NIAAA · UNIVERSITY OF LOUISVILLE · PI Irina A. Kirpich · 2016 to 2026
$17.9M
Novel Therapies for Alcoholic HepatitisU01AA021893 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI MCCLAIN, CRAIG J., MCCULLOUGH, ARTHUR JOSEPH · 2012 to 2017
$6.0M
Oxidized Metabolites of Linoleic Acid in Alcohol-induced Liver InjuryU01AA022489 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FELDSTEIN, ARIEL, MCCLAIN, CRAIG J. · 2014 to 2018
$1.7M
Mechanisms for alcohol induced gut barrier dysfunction in ALDR01AA023681 · NIAAA · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2014 to 2018
$1.6M
Novel therapies in alcoholic hepatitis University of LouisvilleU01AA021901 · NIAAA · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2012 to 2017
$1.5M
Alcohol Liver Disease and Alcohol-Nutrient InteractionsP01AA017103 · NIAAA · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2008 to 2010
$1.3M
Lipid metabolites can both potentiate and treat alcoholic hepatitisU01AA026936 · NIAAA · UNIVERSITY OF LOUISVILLE · PI JOSHI-BARVE, SWATI, MCCLAIN, CRAIG J. · 2018 to 2022
$1.2M
Zinc supplementation in alcoholic cirrhosisK23AA018399 · NIAAA · UNIVERSITY OF LOUISVILLE · PI CAVE, MATTHEW C · 2010 to 2014
$1.0M
Alcohol Pharmacokinetics and Pharmacodynamics in HumansZ01AA000466 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI RAMCHANDANI, VIJAY ARJUN · 2006 to 2008
$762k
BLRD VA I01 BX000350BLRD VA I01 BX002996Intramural NIH HHS Z01 AA000466Intramural NIH HHS Z99 AA999999NCRR NIH HHS P20 RR023523NIAAA NIH HHS K23 AA018399NIAAA NIH HHS L30 AA018643NIAAA NIH HHS P01 AA017103NIAAA NIH HHS P50 AA024337NIAAA NIH HHS R01 AA023681NIAAA NIH HHS U01 AA021893NIAAA NIH HHS U01 AA021901NIAAA NIH HHS U01 AA022489NIAAA NIH HHS U01 AA026936NIGMS NIH HHS P20 GM113226
6 · The paper itself

Abstract

Zinc deficiency is a frequent complication of alcohol abuse for multiple reasons including poor intake, increased excretion, internal redistribution and altered transporters. Zinc deficiency has been postulated to play a role in the development/progression of alcoholic liver disease (ALD). This study aimed to relate serum zinc levels with alcohol intake, serum albumin concentration and markers of inflammation and liver injury. One hundred and eight male and female very heavy drinking (≥10 drinks/day) individuals without clinical evidence of ALD were grouped by serum zinc concentration: normal-zinc group (zinc level≥71 μg/dl) included 67 patients, and low-zinc group (zinc level<71 μg/dl) included 41 patients. Data were collected on demographics, drinking history in last 90 days (heavy drinking days, HDD90 and total drinks, TD90), lifetime drinking history (LTDH) and clinical/ laboratory assessments. Our data show that in a very well-characterized, chronically heavy-drinking population without clinical evidence of liver disease, about 40% of subjects had low serum zinc levels. Frequency of heavy drinking days (HDD90) was significantly higher in the low-zinc group. Total drinks in past 90 days, LTDH and HDD90 showed significant associations with low zinc levels. The group with the low serum zinc had a higher aspartate aminotransferase/alanine aminotransferase ratio (good marker of alcoholic liver disease). Those in the low-zinc group had the lower albumin levels, a marker of hepatic synthetic function, and the highest C-reactive protein level, a biomarker of inflammation.

Indexed as

AdultAgedAlanine TransaminaseAlcoholismAspartate AminotransferasesBilirubinBiomarkersC-Reactive ProteinFemaleHumansLiver Diseases, AlcoholicMaleMiddle AgedSerum Albumin, HumanZincAlanine TransaminaseAspartate AminotransferasesBilirubinBiomarkersC-Reactive ProteinSerum Albumin, HumanZincAlcoholC-reactive proteinDrinking historyLiver injuryZinc

Identifiers

PMID29960116
PMCPMC6129416
OpenAlexW2799843191

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.