Evidence map›Paper›PMID 42215794›Full record

ArticleBiological trace element research2026

Toxic Elements Disrupts Angiogenic Balance in Pathogenesis of Hypertensive Disorders of Pregnancy.

Rupita Kulshrestha, Shefali Singh, Shivani Singh, Juhi Verma, Manish Raj Kulshrestha

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Article in Biological trace element research, 2026. 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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5 · Who and what money

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5 authors.

Rupita KulshresthaDepartment of Obstetrics and Gynecology, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, 226010, Uttar Pradesh, India.
Shefali SinghDepartment of Biochemistry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, 226010, India.
Shivani SinghDepartment of Biochemistry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, 226010, India.
Juhi VermaDepartment of Biochemistry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, 226010, India.
Manish Raj KulshresthaDepartment of Biochemistry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, 226010, India. drmrkul@gmail.com.ORCID http://orcid.org/0000-0002-5355-4539

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertensive disorders of pregnancy (HDP) are a leading cause of maternal and fetal morbidity and mortality, with emerging evidence indicating that trace element imbalances may play a role in their pathogenesis. This study aims at detecting association between heavy metals (Ni, As, Hg, Al, Pb, and Cd), angiogenic markers (PlGF and sFlt-1), their ratio (sFlt-1/PlGF) and risk of developing HDP. This prospective case-control study was conducted at the Department of Obstetrics and Gynecology in collaboration with the Department of Biochemistry at a North Indian tertiary care center. It included 203 pregnant women (HDP) and 199 normotensive pregnant controls. Serum trace elements were analyzed using ICPMS (Nexion 1000, Perkin Elmer), while sFLT-1 and PlGF were analyzed on Cobas e-series 6000 (Roche Diagnostics) using commercially available kits from the same manufacturer. The sFlt-1/PlGF ratio was also calculated. Women with HDP had significantly higher serum Ni (p < 0.017), As (p = 0.001), and Hg (p = 0.001) levels. The median sFlt-1/PlGF ratio was significantly higher in Q4 (50.27; IQR: 14.85-134.68) than in Q1 (34.61; IQR: 17.65-141.58) (p = 0.025). With HDP as the outcome, serum levels of Ni (β = 4.47; p = 0.001), As (β = 0.08; p = 0.001), and Hg (β = 0.51; p = 0.011) were significant risk factors. The Gaussian process classifier and BKMR analysis revealed that Ni, As, and Hg increased the probability of HDP. WQS regression further confirmed Ni as the predominant contributor (94%) to HDP risk, with Hg (1.4%) contributing only moderately. Elevated levels of Ni, As, and Hg were significantly associated with a higher risk of HDP and angiogenic biomarkers.

Indexed as

AngiogenesisHypertension, Pregnancy-InducedMetals, HeavyTrace ElementsAdultBiomarkersCase-Control StudiesFemaleHumansPlacenta Growth FactorPregnancyProspective StudiesVascular Endothelial Growth Factor Receptor-1BiomarkersFLT1 protein, humanMetals, HeavyPGF protein, humanPlacenta Growth FactorTrace ElementsVascular Endothelial Growth Factor Receptor-1Angiogenic biomarkersHypertensive disorders of pregnancy (HDP)PreeclampsiasFlt/PlGF ratioToxic elements

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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.