The significance of mitochondrial haplogroups in preeclampsia risk.


Journal

Pregnancy hypertension
ISSN: 2210-7797
Titre abrégé: Pregnancy Hypertens
Pays: Netherlands
ID NLM: 101552483

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 27 06 2023
revised: 02 10 2023
accepted: 01 11 2023
medline: 5 12 2023
pubmed: 19 11 2023
entrez: 18 11 2023
Statut: ppublish

Résumé

To determine whether mitochondrial haplogroups function as disease-modifiers or as susceptibility factors in preeclampsia using a traditional haplogroup association model. This retrospective study haplotyped 235 control and 78 preeclamptic pregnancies from Denmark using either real-time PCR or Sanger sequencing depending on the rarity of the haplogroup. No significant association between haplogroups and the risk of preeclampsia was found, nor was any role for haplogroups in disease severity uncovered. Mitochondrial haplogroups are not associated with preeclampsia or the severity of preeclampsia in the Danish population. However, this study cannot exclude a role for less common mtDNA variation. Models that can examine these should be applied in preeclamptic patients.

Identifiants

pubmed: 37979242
pii: S2210-7789(23)00369-0
doi: 10.1016/j.preghy.2023.11.001
pii:
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

146-151

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kristina Wendelboe Olsen (K)

Fertility Department, Copenhagen University Hospital Rigshospitalet, 2100 Copenhagen, Denmark.

Paula L Hedley (PL)

Department for Congenital Disorders, Statens Serum Institut, 2300 Copenhagen, Denmark; Brazen Bio, Los Angeles, CA, USA.

Christian M Hagen (CM)

Department for Congenital Disorders, Statens Serum Institut, 2300 Copenhagen, Denmark; Department of Biomedical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

Line Rode (L)

Department of Clinical Biochemistry, Copenhagen University Hospital Rigshospitalet, 2600 Glostrup, Denmark.

Sophie Placing (S)

Department for Congenital Disorders, Statens Serum Institut, 2300 Copenhagen, Denmark.

Karen R Wøjdemann (KR)

Department of Gynecology and Obstetrics, Bornholm Hospital, 3700 Rønne, Bornholm, Denmark.

Anne-Cathrine Shalmi (AC)

Department of Obstetrics, Hillerød Sygehus, 3400 Hillerød, Denmark.

Karin Sundberg (K)

Center of Fetal Medicine, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, 2100 Copenhagen, Denmark.

Anne Nørremølle (A)

Department of Cellular and Molecular Medicine, University of Copenhagen, Denmark.

Ann Tabor (A)

Center of Fetal Medicine, Department of Obstetrics, Copenhagen University Hospital Rigshospitalet, 2100 Copenhagen, Denmark; Department of Clinical Medicine, Faculty of Medical and Health Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

Joanna L Elson (JL)

Department for Congenital Disorders, Statens Serum Institut, 2300 Copenhagen, Denmark; Biosciences Institute Newcastle University, Newcastle, UK; The Centre for Human Metabolomics, North-West University, Potchefstroom, South Africa. Electronic address: j.l.elson@ncl.ac.uk.

Michael Christiansen (M)

Department for Congenital Disorders, Statens Serum Institut, 2300 Copenhagen, Denmark; Department of Biomedical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark.

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Classifications MeSH