Identification of an Epigenetic Signature of Osteoporosis in Blood DNA of Postmenopausal Women
Autor: | David Cheishvili, Ani Arakelian, Niaz Mahmood, Surabhi Parashar, David Goltzman, Moshe Szyf, Richard Kremer, Shafaat A. Rabbani |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Oncology medicine.medical_specialty Bone density Endocrinology Diabetes and Metabolism Osteoporosis Bioinformatics Epigenesis Genetic 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Internal medicine medicine Cluster Analysis Humans Orthopedics and Sports Medicine Epigenetics Aged 030304 developmental biology Aged 80 and over 0303 health sciences Postmenopausal women Genome Human business.industry Reproducibility of Results DNA Methylation DNA Methylation Middle Aged medicine.disease 3. Good health Postmenopause 030104 developmental biology ROC Curve CpG site chemistry 030220 oncology & carcinogenesis DNA methylation Cohort Pyrosequencing CpG Islands Female Identification (biology) business Biomarkers |
Zdroj: | Journal of Bone and Mineral Research. 36:2285-2286 |
ISSN: | 1523-4681 0884-0431 |
DOI: | 10.1002/jbmr.4392 |
Popis: | Osteoporosis is one of the most common age-related progressive bone diseases in elderly people. Approximately one in three women and one in five men are predisposed to developing osteoporosis. In postmenopausal women, a reduction in BMD leads to an increased risk of fractures. In the current study, we delineated the DNA methylation signatures in whole blood samples of postmenopausal osteoporotic women. We obtained whole blood DNA from 22 normal women and 22 postmenopausal osteoporotic women (51 to 89 years old) from the Canadian Multicenter Osteoporosis Study (CaMos) cohort. These DNA samples were subjected to Illumina Infinium human methylation 450 K analysis. Illumina 450K raw data were analyzed by Genome Studio software. Analysis of the female participants with early and advanced osteoporosis resulted in the generation of a list of 1233 differentially methylated CpG sites when compared with age-matched normal women. T test, ANOVA, and post hoc statistical analyses were performed, and 77 significantly differentially methylated CpG sites were identified. From the 13 most significant genes, ZNF267, ABLIM2, RHOJ, CDKL5, and PDCD1 were selected for their potential role in bone biology. A weighted polygenic DNA methylation score of these genes predicted osteoporosis at an early stage with high sensitivity and specificity and correlated with measures of bone density. Pyrosequencing analysis of these genes was performed to validate the results obtained from Illumina 450 K methylation analysis. The current study provides proof of principal for the role of DNA methylation in osteoporosis. Using whole blood DNA methylation analysis, women at risk of developing osteoporosis can be identified before a diagnosis of osteoporosis is made using BMD as a screening method. Early diagnosis will help to select patients who might benefit from early therapeutic intervention. © 2018 American Society for Bone and Mineral Research. |
Databáze: | OpenAIRE |
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