Complete mitochondrial genomes of patients from Thailand with cardiovascular diseases.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 27 01 2024
accepted: 27 06 2024
medline: 11 7 2024
pubmed: 11 7 2024
entrez: 11 7 2024
Statut: epublish

Résumé

Several previous studies have reported that both variation and haplogroups of mitochondrial (mt) DNA were associated with various kinds of diseases, including cardiovascular diseases, in different populations, but such studies have not been carried out in Thailand. Here, we sequenced complete mtDNA genomes from 82 patients diagnosed with three types of cardiovascular disease, i.e., Hypertrophic Cardiomyopathy (HCM) (n = 26), Long Q-T Syndrome (LQTS) (n = 7) and Brugada Syndrome (BrS) (n = 49) and compared these with 750 previously published mitogenome sequences from interviewed normal individuals as a control group. Both patient and control groups are from the same geographic region of northeastern Thailand. We found 9, 2, and 5 novel mutations that were not both damaging and deleterious in HCM, LQTS, and BrS patients, respectively. Haplogroup R9c was significantly associated with HCM (P = 0.0032; OR = 62.42; 95%CI = 6.892-903.4) while haplogroup M12b was significantly associated with LQTS (P = 0.0039; OR = 32.93; 95% CI = 5.784-199.6). None of the haplogroups was found to be significantly associated with BrS. A significantly higher density of mtDNA variants in the rRNA genes was found in patients with HCM and BrS (P < 0.001) than in those with LQTS or the control group. Effects of detected SNPs in either protein coding or tRNA genes of all the mitogenome sequences were also predicted. Interestingly, three SNPs in two tRNA genes (MT-TA m.5618T>C and m.5631G>A heteroplasmic variants in two BrS patients and MT-TQ m.4392C>T novel homoplasmic variant in a HCM patient) were predicted to alter tRNA secondary structure, possibly leading to abnormal tRNA function.

Identifiants

pubmed: 38990956
doi: 10.1371/journal.pone.0307036
pii: PONE-D-24-03721
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0307036

Informations de copyright

Copyright: © 2024 Woravatin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Wipada Woravatin (W)

Department of Biology, Faculty of Science, Khon Kaen University, Khon Kaen, Thailand.

Rattanasak Wongkomonched (R)

Department of Biology, Faculty of Science, Naresuan University, Phitsanulok, Thailand.

Wichittra Tassaneeyakul (W)

Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Mark Stoneking (M)

Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.
Biométrie et Biologie Évolutive, UMR 5558, CNRS & Université de Lyon, Lyon, France.

Pattarapong Makarawate (P)

Department of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Wibhu Kutanan (W)

Department of Biology, Faculty of Science, Khon Kaen University, Khon Kaen, Thailand.
Department of Biology, Faculty of Science, Naresuan University, Phitsanulok, Thailand.

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