Evidence map›Paper›PMID 41602445›Full record

ArticleFrontiers in physiology2025

ADIPOQ polymorphisms and haplotypes affect circulating adiponectin levels and their association with gestational hypertension and preeclampsia.

Ricardo Nodari Fróes de Castro, Daniela Alves Pereira, Juliana de Oliveira Cruz, Ana C Palei, Jackeline S Rangel Machado, Ricardo C Cavalli, Jose E Tanus-Santos, Valéria Cristina Sandrim, Marcelo Rizzatti Luizon

Abstract read
In one paragraph

Article in Frontiers in physiology, 2025. 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
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.

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

9 authors.

Ricardo Nodari Fróes de Castro *Department of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Daniela Alves Pereira *Department of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Juliana de Oliveira CruzDepartment of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Ana C PaleiDepartment of Surgery, University of Mississippi Medical Center, Jackson, MS, United States.
Jackeline S Rangel MachadoDepartment of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Brazil.
Ricardo C CavalliDepartment of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Brazil.
Jose E Tanus-SantosDepartment of Pharmacology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Brazil.
Valéria Cristina Sandrim *Department of Biophysics and Pharmacology, Institute of Biosciences, Universidade Estadual Paulista (UNESP), Botucatu, Brazil.
Marcelo Rizzatti Luizon *Department of Genetics, Ecology and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Imbalance of adipocytokines has been implicated in endothelial dysfunction in hypertensive disorders of pregnancy (HDP). Adiponectin is an adipocytokine that regulates metabolism, insulin sensitivity, and inflammation, and increased adiponectin levels have been associated with mortality in subjects with cardiovascular diseases. Adiponectin also plays a role in trophoblast invasion during placental development. Objectives: We assessed and compared plasma adiponectin levels among healthy pregnant (HP, n = 182), GH (n = 121), and PE (n = 133) women, and examined whether Materials and Methods: Adiponectin concentrations were determined using the Human Adiponectin ELISA kit. Genotypes were determined by Taqman allele discrimination assays. Haplotype frequencies were estimated using Haplo. stats. Multiple logistic/linear regression analyses were adjusted for selected covariates. Results: Plasma adiponectin levels were higher in PE than in HP, including when patients were stratified by body mass index. Regarding rs266729 (C>G) SNP, the GG genotype was associated with risk for GH, and the CG genotype may protect against PE. PE patients carrying the CG and GG genotypes showed higher adiponectin levels than their CC counterparts. The 'G,T,G' haplotype showed higher adiponectin levels in PE than in HP, and the 'C,T,T' haplotype may protect against GH. Conclusion: Our novel findings indicate that

Indexed as

adiponectinADIPOQbiomarkersgenetic polymorphismsgestational hypertensionhaplotypespreeclampsia

Identifiers

PMID41602445
PMCPMC12832239

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.