Evidence map›Paper›PMID 28534210›Full record

ArticleRheumatology international2017

Association study of estrogen receptor alpha gene polymorphisms with bone mass assessed by quantitative ultrasound in young adults.

María Correa-Rodriguez, Jacqueline Schmidt-RioValle, Blanca Rueda-Medina

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Article in Rheumatology international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

María Correa-RodriguezFaculty of Health Sciences, University of Granada (Spain), Av. Ilustración S/N, 18007, Granada, Spain. macoro@ugr.es.
Jacqueline Schmidt-RioValleFaculty of Health Sciences, University of Granada (Spain), Av. Ilustración S/N, 18007, Granada, Spain.
Blanca Rueda-MedinaFaculty of Health Sciences, University of Granada (Spain), Av. Ilustración S/N, 18007, Granada, Spain.
Universidad de Granada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Different genetic variants in estrogen receptor alpha (ESR1) have been shown to influence bone phenotypes including quantitative bone ultrasound in elderly. We aimed to investigate the role of ESR1 polymorphisms in bone mass assessed by calcaneal quantitative ultrasound (QUS) in a population of young adults. The study sample consisted of 466 healthy individuals of Caucasian ancestry (315 females and 152 males) aged 18 and 25 years (median age 20.39 ± 2.70). Six ESR1 polymorphisms (rs302033, rs2982552, rs2982575, rs2504063, rs2234693-PvuII and rs9340799-XbaI) were selected as genetic markers and genotyped. Bone mass in the right calcaneus was estimated with QUS. In the unadjusted analysis, rs2982575 polymorphism was significantly associated with quantitative ultrasound parameter in the whole sample (p = 0.014, β (95% CI) = -0.114 (-1.023, -0.115). However, after adjusting for multiple confounding factors, this association did not remain significant. For the rest of the selected polymorphisms in ESR1, no significant association was observed with calcaneal parameter. Linkage disequilibrium analysis identified a single LD block for the ESR1 gene including PvuII and XbaI SNPs (pair-wise r

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultBone DensityCalcaneusCross-Sectional StudiesEstrogen Receptor alphaFemaleGenetic MarkersHumansMaleOsteoporosisPolymorphism, Single NucleotideRisk FactorsUltrasonographyYoung AdultESR1 protein, humanEstrogen Receptor alphaGenetic MarkersESR1PolymorphismsQuantitative ultrasoundYoung adults

Identifiers

PMID28534210
OpenAlexW2618735259

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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.