Evidence map›Paper›PMID 40080311›Full record

ArticleBiochemical genetics2026

Both Fetal and Maternal Genotypes Affect Preeclampsia Pathogenesis in Iranian Patients.

Veys Hashemnia, Hossein Sadeghi, Asal Honarpour, Kimia Dorraji, Nazanin Haririan, Yasaman Electriciteh, Reza Mirfakhraie

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Article in Biochemical genetics, 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

Authors and funding

7 authors.

Veys HashemniaDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Koodakyar St, Velenjak Ave, Chamran Highway, Tehran, 19395-4719, Iran.
Hossein SadeghiDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Koodakyar St, Velenjak Ave, Chamran Highway, Tehran, 19395-4719, Iran.
Asal HonarpourDepartment of Genetics, Faculty of Biology Science, North Tehran Branch, Islamic Azad University, Tehran, Iran.
Kimia DorrajiDepartment of Genetics, Faculty of Biology Science, North Tehran Branch, Islamic Azad University, Tehran, Iran.
Nazanin HaririanBiology Department, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Yasaman ElectricitehBiology Department, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Reza MirfakhraieDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Koodakyar St, Velenjak Ave, Chamran Highway, Tehran, 19395-4719, Iran. reza_mirfakhraie@yahoo.com.ORCID https://orcid.org/0000-0003-1709-8975

Funding

Current research was financially supported by the Research Department of the School of Medicine, Shahid Beheshti University of Medical Sciences 32899
6 · The paper itself

Abstract

Preeclampsia is a multifactorial disorder that only occurs during pregnancy. Several genome-wide association studies (GWASs) have revealed potential susceptible variants associated with preeclampsia in different populations. GWASs findings in other ethnicities must be replicated in order to confirm the observed genotype-phenotype association. Here, we performed a replication study to investigate the association of three previously reported genome-wide signals, including FLT1rs4769612, FTO rs1421085, and ZNF831 rs259983, with preeclampsia in the Iranian population. A total of 600 subjects were recruited for this study. The maternal group included 200 preeclamptic patients and 200 healthy normotensive pregnant women. The fetal group included 100 individuals born of preeclamptic pregnancies and 100 individuals born from healthy pregnancies. The tetra-primer amplification refractory mutation system-polymerase chain reaction (TP-ARMS PCR) technique was used for genotyping the rs4769612, rs1421085, and rs259983 variants. The fetal genotype of rs4769612 (FLT1) was associated with preeclampsia risk under the recessive inheritance model. Moreover, fetal rs1421085 (FTO) increased the risk of preeclampsia under dominant and over-dominant inheritance models. Regarding ZNF831 rs259983, only the maternal genotype was associated with preeclampsia under the dominant model, and no association was detected between the fetal genotype and the disease risk. Although the present results showed discrepancies with previous studies considering the association of maternal or fetal genotypes with preeclampsia, all three studied polymorphisms were related to the disease risk in the Iranian population. Based on our study, rs4769612, rs1421085, and rs259983 were associated with the risk of preeclampsia in the Iranian population.

Indexed as

Polymorphism, Single NucleotidePre-EclampsiaVascular Endothelial Growth Factor Receptor-1AdultCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansIranPregnancyFLT1 protein, humanVascular Endothelial Growth Factor Receptor-1FLT1 rs4769612FTO rs1421085GWASPreeclampsiaZNF831 rs259983

Identifiers

PMID40080311

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