Evidence map›Paper›PMID 35689735›Full record

ArticleJournal of assisted reproduction and genetics2022

MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study.

Lívia Reis Silva, Anderson Sanches Melo, Karina Bezerra Salomão, Suleimy Cristina Mazin, Luiz Gonzaga Tone, Viviane Cunha Cardoso, Rosana Maria Dos Reis, Cristiana Libardi Miranda Furtado, Rui Alberto Ferriani

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 2 institutions in 1 country.

Lívia Reis Silva *Department of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Anderson Sanches Melo *Department of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Karina Bezerra SalomãoDepartment of Pediatrics, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirão Preto, Brazil.
Suleimy Cristina MazinDepartment of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Luiz Gonzaga ToneDepartment of Pediatrics, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirão Preto, Brazil.
Viviane Cunha CardosoDepartment of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Rosana Maria Dos ReisDepartment of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Cristiana Libardi Miranda Furtado *Department of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil. clibardim@gmail.com.ORCID http://orcid.org/0000-0002-8711-8225
Rui Alberto Ferriani *Department of Gynecology and Obstetrics, Ribeirao Preto Medical School (FMRP), University of Sao Paulo (USP), Ribeirão Preto, Brazil.
Universidade de São Paulo · BRUniversidade de Ribeirão Preto · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/26152-7
6 · The paper itself

Abstract

purposeTo evaluate the genetic variants related to polycystic ovary syndrome (PCOS) and its metabolic complications in girls born small for gestational age (SGA).

designRetrospective birth cohort study. MATERIALS AND

methodsWe evaluated 66 women of reproductive age born at term (37-42 weeks of gestational age) according to the birth weight in relation to gestational age: 26 SGA and 40 AGA (Adequate for gestational age). Anthropometric and biochemical characteristics were measured, as well as the PCOS prevalence. We analyzed 48 single nucleotide polymorphisms (SNPs) previously associated with PCOS and its comorbidities using TaqMan Low-Density Array (TLDA). miRNet and STRING databases were used to predict target and disease networks.

resultsAnthropometric and biochemical characteristics did not differ between the SGA and AGA groups, as well as insulin resistance and PCOS prevalence. Two SNPs were not in Hardy-Weinberg equilibrium, the rs2910164 (MIR146A C > G) and rs182052 (ADIPOQ G > A). The rs2910164 minor allele frequency (MAF) was increased in SGA (OR, 2.77; 95%; CI, 1.22-6.29), while the rs182052 was increased AGA (OR, 0.34; 95%; CI, 0.13 - 0.88). The alleles related to reduced miRNA-146a (C) and ADIPOQ (A) activity showed increased frequency in SGA. The mature miR-146a targets 319 genes, been the CXCR4, TMEM167A and IF144L common targets and contributes to PCOS. The ADIPOQ main protein interactions were ERP44, PPARGCIA and CDH13.

conclusionsThe miR-146a (rs2910164) and ADIPOQ (rs182052) allelic variants are related to birth weight in SGA and may predict health-related outcomes, such as PCOS and obesity risk.

Indexed as

MicroRNAsPolycystic Ovary SyndromeAdiponectinAdultBirth WeightCohort StudiesFemaleGestational AgeHumansInfantInfant, NewbornInfant, Small for Gestational AgeRetrospective StudiesAdiponectinADIPOQ protein, humanMicroRNAsAdiponectinMaternal–fetal interactionMicro-RNAsSingle nucleotide polymorphismsSmall for gestational age

Identifiers

PMID35689735
PMCPMC9428086
OpenAlexW4282935787

What OpenQuestion holds

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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.