MMP-2 and MMP-9 Polymorphisms and Preeclampsia Risk in Tunisian Arabs: A Case-Control Study.

MMP-2 MMP-9 SNPs genotyping preeclampsia

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
16 Jun 2021
Historique:
received: 11 05 2021
revised: 03 06 2021
accepted: 10 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

The abnormal production of matrix metalloproteinases (MMPs), especially MMP-9 and MMP-2, plays a pivotal role in hypertensive disorders of pregnancy, and as such, can influence the development of preeclampsia. These alterations may result from functional genetic polymorphisms in the promoter region of MMP-9 and MMP-2 genes, which modify MMP-9 and MMP-2 expression. We investigated the association of MMP-9 polymorphism rs3918242 (-1562 C>T) and MMP-2 polymorphism rs2285053 (-735 C>T) with the risk of preeclampsia. This case-control study was conducted on 345 women with preeclampsia and 281 age-matched women with normal pregnancies from Tunisian hospitals. Genomic DNA was extracted from whole blood collected at delivery. Genotypes for -1562 C>T and -735 C>T polymorphisms were performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). An increased frequency of heterozygous MMP-9 -1562 C/T genotype carriers was observed in women with preeclampsia compared to healthy controls (

Identifiants

pubmed: 34208487
pii: jcm10122647
doi: 10.3390/jcm10122647
pmc: PMC8234886
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : CIHR
ID : PJT-169020
Pays : Canada
Organisme : Ministry of higher education and scientific research Tunisia
ID : none

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Auteurs

Marwa Ben Ali Gannoun (MBA)

Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir 5000, Tunisia.
Laboratory of Histology Embryology and Cytogenetics, Faculty of Medicine, University of Monastir, Monastir 5000, Tunisia.

Nozha Raguema (N)

Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir 5000, Tunisia.
Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC H2X 0A9, Canada.
School of Kinesiology and Physical Activity Sciences, Université de Montréal, Montréal, QC H3T 1J4, Canada.

Hedia Zitouni (H)

Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir 5000, Tunisia.

Meriem Mehdi (M)

Laboratory of Cytogenetics and Reproductive Biology, Center of Maternity and Neonatology Monastir, Fattouma Bourguiba University Teaching Hospital, Monastir 5000, Tunisia.

Ondrej Seda (O)

The First Faculty of Medicine and General University Hospital, Institute of Biology and Medical Genetics, Charles University, 12800 Prague, Czech Republic.

Touhami Mahjoub (T)

Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir 5000, Tunisia.

Julie L Lavoie (JL)

Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montréal, QC H2X 0A9, Canada.
School of Kinesiology and Physical Activity Sciences, Université de Montréal, Montréal, QC H3T 1J4, Canada.

Classifications MeSH