Evidence map›Paper›PMID 20951195›Full record

ArticleExperimental gerontology2011

Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects.

Maria De Luca, Paolina Crocco, Howard Wiener, Hemant K Tiwari, Giuseppe Passarino, Giuseppina Rose

Abstract read
In one paragraph

Article in Experimental gerontology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
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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

6 authors at 2 institutions in 2 countries.

Maria De LucaDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35294, USA. mdeluca2@uab.edu
Paolina Crocco
Howard Wiener
Hemant K Tiwari
Giuseppe Passarino
Giuseppina Rose
University of Alabama at Birmingham · USUniversity of Calabria · IT

Funding

Genetic control of quantitative traits associated with the metabolic syndromeR01DK084219 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DE LUCA, MARIA · 2010 to 2013
$1.3M
NIDDK NIH HHS R01 DK084219NIDDK NIH HHS R01DK084219
6 · The paper itself

Abstract

Laminins are large heterotrimeric glycoproteins found in basement membranes where they play an essential role in cell-matrix adhesion, migration, growth, and differentiation of various cell types. Previous work reported that a genetic variant located within the intron 1 of LAMA5 (rs659822) was associated with anthropometric traits and HDL-cholesterol levels in a cohort of premenopausal women. The present study aimed to investigate the effect of LAMA5 rs659822 on anthropometric traits, lipid profile, and fasting glucose levels in an Italian cohort of 667 healthy elderly subjects (aged 64-107years). We also tested for association between these traits and the single nucleotide polymorphism (SNP) rs13043313, which was previously shown to control variation in LAMA5 transcript abundance in the liver of Caucasians. In age- and gender-adjusted linear regression analyses, we did not find association of rs13043313 with any of the traits. However, under an additive model, the minor C-allele of LAMA5 rs659822 was associated with shorter stature (p = 0.007) and higher fasting glucose levels (p = 0.02). Moreover, subjects homozygous for the C-allele showed on average 6% and 10% lower total cholesterol (p = 0.034) and LDL-cholesterol (p = 0.016) levels, respectively, than those carrying at least one T allele, assuming a recessive model. Finally, in analyses stratified by age groups (age range 64-89 and 90-107 years), we found that the C-allele was additively associated with increased body weight (p = 0.018) in the age group 64-89 years, whereas no association was found in the age group 90-107 years. In conclusion, this study provides evidence that LAMA5 rs659822 regulates anthropometric and metabolic traits in elderly people. Future studies are warranted to replicate these findings in independent and larger populations and to investigate whether rs659822 is the causal variant responsible for the observed associations.

Indexed as

Genetic VariationAgedAged, 80 and overAgingAnthropometryBlood GlucoseCohort StudiesFemaleGenotypeHumansIntronsItalyLamininLipidsMaleMetabolomeBlood GlucoseLamininlaminin alpha5Lipids

Identifiers

PMID20951195
PMCPMC2998567
OpenAlexW2020361179

What OpenQuestion holds

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Read underepoch 390

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.