Evidence map›Paper›PMID 25505833›Full record

ArticleGenetics and molecular biology2014

The lactase persistence genotype is a protective factor for the metabolic syndrome.

Deise C Friedrich, Fabiana M de Andrade, Marilu Fiegenbaum, Silvana de Almeida, Vanessa S Mattevi, Sidia M Callegari-Jacques, Mara H Hutz

Open access · goldAbstract read
In one paragraph

Article in Genetics and molecular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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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

7 authors at 3 institutions in 1 country.

Deise C FriedrichDepartamento de Genética , Universidade Federal do Rio Grande do Sul , Porto Alegre, RS , Brazil .
Fabiana M de AndradeInstituto de Ciências da Saúde , Universidade Feevale , Novo Hamburgo, RS , Brazil .
Marilu FiegenbaumPós-Graduação em Ciências da Saúde , Universidade Federal de Ciências da Saúde de Porto Alegre , Porto Alegre, RS , Brazil .
Silvana de AlmeidaPós-Graduação em Ciências da Saúde , Universidade Federal de Ciências da Saúde de Porto Alegre , Porto Alegre, RS , Brazil .
Vanessa S MatteviPós-Graduação em Ciências da Saúde , Universidade Federal de Ciências da Saúde de Porto Alegre , Porto Alegre, RS , Brazil .
Sidia M Callegari-JacquesDepartamento de Estatística , Universidade Federal do Rio Grande do Sul , Porto Alegre, RS , Brazil .
Mara H HutzDepartamento de Genética , Universidade Federal do Rio Grande do Sul , Porto Alegre, RS , Brazil .
Universidade Federal de Ciências da Saúde de Porto Alegre · BRUniversidade Federal do Rio Grande do Sul · BRUniversidade Feevale · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Metabolic Syndrome (MetS) is defined as a pattern of metabolic disturbances, which include central obesity, insulin resistance and hyperglycemia, dyslipidemia, and hypertension. Milk has been promoted as a healthy beverage that can improve the management of MetS. Most human adults, however, down-regulate the production of intestinal lactase after weaning. Lactase encoded by the LCT gene is necessary for lactose digestion. The -13910C > T SNP (rs4988235) is responsible for the lactase persistence phenotype in European populations. We herein investigated whether the lactase persistence genotype is also associated with the MetS in subjects from a Brazilian population of European descent. This study consisted of 334 individuals (average age of 41 years) genotyped by PCR-based methods for the -13910C > T SNP. Clinical data were assessed and the genotypes were tested for their independent contribution to the MetS using chi-square tests and multiple logistic regression analysis. Univariate analyses showed that hypertension and MetS prevalence were higher in individuals with the lactase non-persistence genotype than in lactase persistence subjects. Furthermore, lactase persistence was associated with a lower risk for MetS (OR = 0.467; 95% CI 0.264-0.824; p = 0.009). These results suggest that LCT genotypes can be a valuable tool for the management of MetS treatment.

Indexed as

hypolactasialactase persistencelactosemetabolic syndrome

Identifiers

PMID25505833
PMCPMC4261958
OpenAlexW2003113207

What OpenQuestion holds

Textmetadata
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Registered trials

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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.