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

Author:

Ding Binrong1,Zhang Xuewei2,Wan Zhengqing3,Tian Feng4,Ling Jie5,Tan Jieqiong6789,Peng Xiaoqing6789

Affiliation:

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

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

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

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

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

6. Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha 410000, China

7. Institute of Molecular Precision Medicine, Xiangya Hospital, Central South University, Changsha 410000, China

8. Hunan Key Laboratory of Molecular Precision Medicine, Changsha 410000, China

9. Hunan International Scientific and Technological Cooperation Base of Neurodegenerative and Neurogenetic Diseases, Changsha 410000, China

Abstract

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.

Funder

Natural Science Foundation of Hunan Province

Central South University Innovation-Driven Research Programme

Hunan Provincial Maternal and Child Health Care Hospital

Publisher

MDPI AG

Subject

Clinical Biochemistry

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