Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.

<h4>Background</h4>Elevated baseline circulating alanine aminotransferase (ALT) level has been demonstrated to be associated with an increased risk of the metabolic syndrome (MetS), but the nature of the dose-response relationship is uncertain.<h4>Methods</h4>We performed a s...

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Main Authors: Setor K Kunutsor, Dorothy Seddoh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24781277/pdf/?tool=EBI
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spelling doaj-07a5d0eec07147f5b7a175e14e9b94b02021-03-04T09:29:29ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9606810.1371/journal.pone.0096068Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.Setor K KunutsorDorothy Seddoh<h4>Background</h4>Elevated baseline circulating alanine aminotransferase (ALT) level has been demonstrated to be associated with an increased risk of the metabolic syndrome (MetS), but the nature of the dose-response relationship is uncertain.<h4>Methods</h4>We performed a systematic review and meta-analysis of published prospective cohort studies to characterize in detail the nature of the dose-response relationship between baseline ALT level and risk of incident MetS in the general population. Relevant studies were identified in a literature search of MEDLINE, EMBASE, and Web of Science up to December 2013. Prospective studies in which investigators reported relative risks (RRs) of MetS for 3 or more categories of ALT levels were eligible. A potential nonlinear relationship between ALT levels and MetS was examined using restricted cubic splines.<h4>Results</h4>Of the 489 studies reviewed, relevant data were available on 29,815 non-overlapping participants comprising 2,125 incident MetS events from five prospective cohort studies. There was evidence of a linear association (P for nonlinearity=0.38) between ALT level and risk of MetS, characterised by a graded increase in MetS risk at ALT levels 6-40 U/L. The risk of MetS increased by 14% for every 5 U/L increment in circulating ALT level (95% CI: 12-17%). Evidence was lacking of heterogeneity and publication bias among the contributing studies.<h4>Conclusions</h4>Baseline ALT level is associated with risk of the MetS in a linear dose-response manner. Studies are needed to determine whether the association represents a causal relationship.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24781277/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Setor K Kunutsor
Dorothy Seddoh
spellingShingle Setor K Kunutsor
Dorothy Seddoh
Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
PLoS ONE
author_facet Setor K Kunutsor
Dorothy Seddoh
author_sort Setor K Kunutsor
title Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
title_short Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
title_full Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
title_fullStr Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
title_full_unstemmed Alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
title_sort alanine aminotransferase and risk of the metabolic syndrome: a linear dose-response relationship.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description <h4>Background</h4>Elevated baseline circulating alanine aminotransferase (ALT) level has been demonstrated to be associated with an increased risk of the metabolic syndrome (MetS), but the nature of the dose-response relationship is uncertain.<h4>Methods</h4>We performed a systematic review and meta-analysis of published prospective cohort studies to characterize in detail the nature of the dose-response relationship between baseline ALT level and risk of incident MetS in the general population. Relevant studies were identified in a literature search of MEDLINE, EMBASE, and Web of Science up to December 2013. Prospective studies in which investigators reported relative risks (RRs) of MetS for 3 or more categories of ALT levels were eligible. A potential nonlinear relationship between ALT levels and MetS was examined using restricted cubic splines.<h4>Results</h4>Of the 489 studies reviewed, relevant data were available on 29,815 non-overlapping participants comprising 2,125 incident MetS events from five prospective cohort studies. There was evidence of a linear association (P for nonlinearity=0.38) between ALT level and risk of MetS, characterised by a graded increase in MetS risk at ALT levels 6-40 U/L. The risk of MetS increased by 14% for every 5 U/L increment in circulating ALT level (95% CI: 12-17%). Evidence was lacking of heterogeneity and publication bias among the contributing studies.<h4>Conclusions</h4>Baseline ALT level is associated with risk of the MetS in a linear dose-response manner. Studies are needed to determine whether the association represents a causal relationship.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24781277/pdf/?tool=EBI
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