ArticleFrontiers in physiology2025
ADIPOQ polymorphisms and haplotypes affect circulating adiponectin levels and their association with gestational hypertension and preeclampsia.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.