Evidence map›Paper›PMID 25759378›Full record

Trial reportPhysiological genomics2015

A common variant in the CLDN7/ELP5 locus predicts adiponectin change with lifestyle intervention and improved fitness in obese individuals with diabetes.

L Maria Belalcazar, George D Papandonatos, Jeanne M McCaffery, Inga Peter, Nicholas M Pajewski, Bahar Erar, Nicholette D Allred, Ashok Balasubramanyam, Donald W Bowden, Ariel Brautbar and 4 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Physiological genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact, top 94% 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, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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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

14 authors at 8 institutions in 1 country.

L Maria BelalcazarDepartment of Medicine, University of Texas Medical Branch, Galveston, Texas; lmbelalc@utmb.edu.
George D PapandonatosDepartment of Biostatistics, Brown University, Providence, Rhode Island;
Jeanne M McCafferyWeight Control and Diabetes Research Center, Department of Psychiatry and Human Behavior, The Miriam Hospital and Brown Medical School, Providence, Rhode Island;
Inga PeterDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York;
Nicholas M PajewskiDepartment of Biostatistical Sciences, Wake Forest University Health Sciences, Winston-Salem, North Carolina;
Bahar ErarDepartment of Biostatistics, Brown University, Providence, Rhode Island;
Nicholette D AllredDepartment of Biochemistry and Center for Genomics and Personalized Medicine Research, Wake Forest University Health Sciences, Winston-Salem, North Carolina;
Ashok BalasubramanyamDepartment of Medicine, Baylor College of Medicine, Houston, Texas;
Donald W BowdenDepartment of Biochemistry and Center for Genomics and Personalized Medicine Research, Wake Forest University Health Sciences, Winston-Salem, North Carolina;
Ariel BrautbarDepartment of Medicine, Baylor College of Medicine, Houston, Texas;
F Xavier Pi-SunyerDepartment of Medicine, Columbia University, St. Luke's-Roosevelt Hospital, New York, New York;
Christie M BallantyneDepartment of Medicine, Baylor College of Medicine, Houston, Texas; Center for Cardiovascular Disease Prevention, Methodist De Bakey Heart and Vascular Center, Houston, Texas; and.
Gordon S HugginsMCRI Center for Translational Genomics, Tufts Medical Center, Boston, Massachusetts.
Look AHEAD Research Group
Brown University · USWake Forest University · USBaylor College of Medicine · USHouston Methodist · USIcahn School of Medicine at Mount Sinai · USSt. Luke's-Roosevelt Hospital Center · USThe University of Texas Medical Branch at Galveston · USTufts Medical Center · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1986 to 2026
$41.4M
RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
Genetic and behavioral effects on high-density lipoprotein: The Look AHEAD StudyR01DK090043 · NIDDK · MIRIAM HOSPITAL · PI MCCAFFERY, JEANNE M · 2011 to 2013
$532k
NCRR NIH HHS UL1 RR025758NHLBI NIH HHS HL-09051401NIDDK NIH HHS DK-090043NIDDK NIH HHS P30 DK017047NIDDK NIH HHS P30 DK026687NIDDK NIH HHS R01 DK090043
6 · The paper itself

Abstract

Overweight/obese individuals with Type 2 diabetes have low adiponectin levels, which may improve with lifestyle changes. We investigated whether genetic variants associated with adiponectin levels in genome-wide association studies (GWAS) would also be related with adiponectin changes in response to an intensive lifestyle intervention (ILI), potentially through mechanisms altering the adipose microenvironment via weight loss and/or improved cardiorespiratory fitness. Look AHEAD was a randomized trial comparing the cardiovascular benefits of ILI-induced weight loss and physical activity compared with diabetes support and education among overweight/obese individuals with Type 2 diabetes. In a subsample of Look AHEAD with adiponectin data and genetic consent (n=1,351), we evaluated the effects of 24 genetic variants, demonstrated by GWAS to be cross-sectionally associated with adiponectin, on adiponectin change 1-yr postintervention. We explored via mediational analyses whether any differential effects by treatment arm were occurring through weight loss and/or improved fitness. A variant, rs222857, in the CLDN7 locus, potentially associated with epithelial barrier integrity and tight junction physiology, and a putative cis expression quantitative trail locus for elongator acetyltransferase complex subunit 5 (ELP5), predicted adiponectin increases within ILI (log-adiponectin in overall sample per copy: β±SE=0.05±0.02, P=0.008; in non-Hispanic whites: 0.06±0.02, P=0.009). The favorable effects of rs222857 (minor allele frequency 45.5%) appeared to be mediated by mechanisms associated with improved fitness, and not weight loss. This is the first study to identify a genetic variant that modifies adiponectin response to lifestyle intervention in overweight/obese diabetic individuals.

Indexed as

Life StylePhysical FitnessAdiponectinAdiposityAgedClaudinsDiabetes Mellitus, Type 2FemaleGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedObesityPolymorphism, Single NucleotideAdiponectinADIPOQ protein, humanClaudinsCLDN7 protein, humanadipose tissueDERP6Elongatorepithelial permeabilityexerciselifestyle interventionLook AHEADmediationp53r3507506sirtuintight junctionweight loss

Identifiers

PMID25759378
PMCPMC4451387
OpenAlexW1990709329

What OpenQuestion holds

Textmetadata
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.