Evidence map›Paper›PMID 25396734›Full record

ArticlePloS one2014

Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women.

Qiu-Hong Zhou, Lan-Juan Zhao, Ping Wang, Rhamee Badr, Xiao-Jing Xu, Feng-Xiao Bu, Joan Lappe, Robert Recker, Yu Zhou, An Ye and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 3 institutions in 2 countries.

Qiu-Hong ZhouDepartment of Endocrinology, Xiangya Hospital, Central South University, Changsha Hunan, 410008, China.
Lan-Juan ZhaoOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America; Department of Biostatistics & Bioinformatics, School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Ping WangDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha Hunan, 410008, China.
Rhamee BadrTulane University School of Medicine, New Orleans, Louisiana, 70112, United States of America.
Xiao-Jing XuOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America.
Feng-Xiao BuOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America.
Joan LappeOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America.
Robert ReckerOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America.
Yu ZhouOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America; Department of Biostatistics & Bioinformatics, School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, 70112, United States of America.
An YeOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America; Department of Biostatistics & Bioinformatics, School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Bo-Ting ZhouOsteoporosis Research Center, Creighton University Medical Center, Creighton University, 601 N 30th ST, Suite 4820, Omaha, Nebraska, 68131, United States of America; Department of Pharmacy, Xiangya Hospital, Central South University, Changsha Hunan, 410008, China.
CHI Health Creighton University Medical Center - Bergan Mercy · USCentral South University · CNTulane University · US

Funding

Clinical Trial of Vitamin D3 to Reduce Cancer Risk in Postmenopausal WomenR01CA129488 · NCI · CREIGHTON UNIVERSITY · PI LAPPE, JOAN · 2009 to 2013
$4.5M
NCI NIH HHS 3R01CA129488-01A2S2NCI NIH HHS R01 CA129488
6 · The paper itself

Abstract

summaryThree genes, including EGFR (epidermal growth factor receptor), CALM3 (calmodulin 3, calcium-modulated protein 3) and SMARCD1 (SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily d member 1), play different roles in bone and/or fat metabolism in Caucasian women. In this population-based investigation of 870 unrelated postmenopausal Caucasian women, CALM3 polymorphisms were significantly associated with femoral neck bone mineral density (FNK BMD), hip BMD and spine BMD. Age and tobacco status also affected BMD levels and were therefore corrected for in our statistical analysis.

introductionEGFR, CALM3 and SMARCD1 play roles in bone and/or fat metabolism. However, the correlations between the polymorphisms of these three genes and body composition levels, including BMD, remain to be determined. MATERIALS AND

methodsA population-based investigation of 870 white women was conducted. Forty-four SNPs (single nucleotide polymorphisms) in EGFR, CALM3 and SMARCD1 were chosen by the software, including those of potential functional importance. The candidate SNPs were genotyped by the KASPar assay for an association analysis with body composition levels. The correlation analysis was assessed by the Pearson's product-moment correlation coefficient and Spearman rank-order correlation tests, and the family-wise error was corrected using the Wald test implemented in PLINK.

resultsThe SNP rs12461917 in the 3'-flanking region of the CALM3 gene was significantly associated with FNK BMD (P = 0.001), hip BMD (P<0.001) and spine BMD (P = 0.001); rs11083838 in the 5'-flanking region of CALM3 gene was associated with spine BMD (P = 0.009). After adjusting for multiple comparisons, rs12461917 remained significant (P-adjusted = 0.033 for FNK BMD, P-adjusted = 0.006 for hip BMD and P-adjusted = 0.018 for spine BMD).

conclusionsOur data show that polymorphisms of the CALM3 gene in Caucasian women may contribute to variations in the BMD of the hip, spine and femoral neck.

Indexed as

Genetic Association StudiesBody CompositionBone DensityCalmodulinChromosomal Proteins, Non-HistoneErbB ReceptorsFemaleHumansMiddle AgedPolymorphism, Single NucleotideTranscription FactorsWhite PeopleCalmodulinChromosomal Proteins, Non-HistoneEGFR protein, humanErbB ReceptorsSMARCD1 protein, humanTranscription Factors

Identifiers

PMID25396734
PMCPMC4232396
OpenAlexW1967580609

What OpenQuestion holds

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LicenceCC BY
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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.