Characterization of Mitochondrial DNA Methylation of Alzheimer's Disease in Plasma Cell-Free DNA.

Alzheimer’s disease cell-free DNA mitochondrial DNA methylation noninvasive diagnosis

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
12 Jul 2023
Historique:
received: 17 05 2023
revised: 29 06 2023
accepted: 10 07 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Noninvasive diagnosis of Alzheimer's disease (AD) is important for patients. Significant differences in the methylation of mitochondrial DNA (mtDNA) were found in AD brain tissue. Cell-free DNA (cfDNA) is a noninvasive and economical diagnostic tool. We aimed to characterize mtDNA methylation alterations in the plasma cfDNA of 31 AD patients and 26 age- and sex-matched cognitively normal control subjects. We found that the mtDNA methylation patterns differed between AD patients and control subjects. The mtDNA was predominantly hypomethylated in the plasma cfDNA of AD patients. The hypomethylation sites or regions were mainly located in mt-rRNA, mt-tRNA, and D-Loop regions. The hypomethylation of the D-Loop region in plasma cfDNA of AD patients was consistent with that in previous studies. This study presents evidence that hypomethylation in the non-protein coding region of mtDNA may contribute to the pathogenesis of AD and potential application for the diagnosis of AD.

Identifiants

pubmed: 37510095
pii: diagnostics13142351
doi: 10.3390/diagnostics13142351
pmc: PMC10378411
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Natural Science Foundation of Hunan Province
ID : 2022JJ30694
Organisme : Central South University Innovation-Driven Research Programme
ID : 2023CXQD066
Organisme : Hunan Provincial Maternal and Child Health Care Hospital
ID : KF2021001

Références

Front Endocrinol (Lausanne). 2023 Jan 16;13:1059120
pubmed: 36726473
Front Cell Dev Biol. 2020 Nov 16;8:581882
pubmed: 33304899
Epigenomics. 2018 Nov;10(11):1431-1443
pubmed: 30088417
Forensic Sci Int Genet. 2016 Sep;24:75-82
pubmed: 27344518
Front Immunol. 2019 May 09;10:1064
pubmed: 31143191
Nat Commun. 2020 Aug 28;11(1):4269
pubmed: 32859890
Am J Pathol. 2016 Feb;186(2):385-97
pubmed: 26776077
Genome Res. 2012 Feb;22(2):407-19
pubmed: 21613409
Neurochem Res. 2021 Mar;46(3):564-572
pubmed: 33580369
J Steroid Biochem Mol Biol. 2016 Jun;160:134-47
pubmed: 26969397
Stem Cells Int. 2017;2017:1764549
pubmed: 28484495
Toxicology. 2018 Sep 1;408:54-61
pubmed: 29940200
Part Fibre Toxicol. 2013 May 08;10:18
pubmed: 23656717
Sci Rep. 2016 Mar 21;6:23421
pubmed: 26996456
Int J Mol Sci. 2022 May 12;23(10):
pubmed: 35628202
Curr Pharm Des. 2020;26(1):103-109
pubmed: 31755379
J Alzheimers Dis. 2017;59(2):559-564
pubmed: 28655136
Clin Epigenetics. 2020 Sep 11;12(1):137
pubmed: 32917270
Clin Epigenetics. 2022 Jan 4;14(1):2
pubmed: 34983647
Biochem Biophys Res Commun. 2019 Nov 26;520(1):41-46
pubmed: 31564416
Mol Neurodegener. 2020 May 29;15(1):30
pubmed: 32471464
Nat Rev Clin Oncol. 2013 Aug;10(8):472-84
pubmed: 23836314
J Alzheimers Dis. 2010;20 Suppl 2:S265-79
pubmed: 20442494
Mol Med Rep. 2015 Nov;12(5):7033-8
pubmed: 26323487
Front Cell Dev Biol. 2021 Aug 27;9:688789
pubmed: 34513831
Diagnostics (Basel). 2022 Jul 29;12(8):
pubmed: 36010184
Mol Med Rep. 2017 Oct;16(4):5347-5353
pubmed: 28849075
Mol Neurodegener. 2021 Nov 6;16(1):75
pubmed: 34742335
Hum Mol Genet. 2018 Mar 1;27(5):891-900
pubmed: 29340697
J Am Heart Assoc. 2016 Apr 22;5(4):
pubmed: 27107129
Int J Mol Med. 2021 Jan;47(1):161-170
pubmed: 33416107
Nature. 2022 Nov;611(7934):105-114
pubmed: 36198798
Epigenetics. 2021 Jan-Feb;16(2):121-131
pubmed: 32657220
Mol Neurodegener. 2021 Apr 26;16(1):28
pubmed: 33902654
Trends Biochem Sci. 2007 Mar;32(3):111-7
pubmed: 17291767
Mol Med Rep. 2012 Jul;6(1):125-30
pubmed: 22505229
Aging (Albany NY). 2016 Apr;8(4):636-41
pubmed: 26887692
Exp Mol Med. 2015 Mar 13;47:e150
pubmed: 25766619
Mol Cell Biol. 2013 Jul;33(14):2683-90
pubmed: 23671186
N Engl J Med. 1998 Dec 10;339(24):1734-8
pubmed: 9845707
Mitochondrion. 2016 Mar;27:40-7
pubmed: 26910457
Neuropathol Appl Neurobiol. 1997 Aug;23(4):315-21
pubmed: 9292870
Neurogenetics. 1999 Apr;2(2):121-7
pubmed: 10369889
Commun Biol. 2021 Jan 8;4(1):61
pubmed: 33420340
Alzheimers Dement. 2015 Mar;11(3):332-84
pubmed: 25984581
Epigenomics. 2015 Aug;7(5):707-16
pubmed: 26343273
Mol Neurobiol. 2012 Aug;46(1):186-93
pubmed: 22833458
EBioMedicine. 2015 Apr 1;2(4):294-305
pubmed: 26086035
Pharmacol Rev. 2022 Jan;74(1):1-17
pubmed: 34987086
Genet Med. 2020 May;22(5):917-926
pubmed: 31965079
Front Genet. 2017 Nov 01;8:166
pubmed: 29163634
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):E1826-34
pubmed: 26976580
Epigenomics. 2014;6(6):665-75
pubmed: 25531259
Alzheimers Dement. 2011 May;7(3):263-9
pubmed: 21514250
Int J Mol Sci. 2021 Apr 27;22(9):
pubmed: 33925624
Nature. 2010 Mar 4;464(7285):104-7
pubmed: 20203610
Clin Epigenetics. 2017 May 3;9:47
pubmed: 28473874

Auteurs

Binrong Ding (B)

Department of Geriatrics, The Third Xiangya Hospital, Central South University, Changsha 410000, China.

Xuewei Zhang (X)

Health Management Center, Xiangya Hospital, Central South University, Changsha 410000, China.

Zhengqing Wan (Z)

Hengyang Medical School, University of South China, Hengyang 421001, China.

Feng Tian (F)

The 8 Ward, The Ninth Hospital of Changsha, Changsha 410000, China.

Jie Ling (J)

Medical Functional Experiment Center, School of Basic Medicine, Central South University, Changsha 410000, China.

Jieqiong Tan (J)

Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha 410000, China.
Institute of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha 410000, China.
Hunan Key Laboratory of Molecular Precision Medicine, Changsha 410000, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha 410000, China.

Xiaoqing Peng (X)

Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha 410000, China.
Institute of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha 410000, China.
Hunan Key Laboratory of Molecular Precision Medicine, Changsha 410000, China.
Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha 410000, China.

Classifications MeSH