The influence of aging on the methylation status of brain-derived neurotrophic factor gene in blood

被引:6
|
作者
Ihara, Kazushige [1 ]
Fuchikami, Manabu
Hashizume, Masahiro [3 ]
Okada, Satoshi [2 ,11 ]
Kawai, Hisashi [4 ]
Obuchi, Shuichi [4 ]
Hirano, Hirohiko [5 ]
Fujiwara, Yoshinori [6 ]
Hachisu, Mitsugu [7 ]
Hongyong, Kim [8 ]
Morinobu, Shigeru [9 ,10 ]
机构
[1] Hirosaki Univ, Grad Sch Med, Dept Social Med, Aomori, Japan
[2] Hirosaki Univ, Grad Sch Biomed Sci, Div Frontier, Dept Psychiat & Neurosci, Hiroshima, Japan
[3] Toho Univ, Fac Med, Dept Psychosomat Med, Tokyo, Japan
[4] Tokyo Metropolitan Inst Gerontol, Human Care Res Team, Tokyo, Japan
[5] Tokyo Metropolitan Geriatr Hosp, Dept Dent, Tokyo, Japan
[6] Tokyo Metropolitan Inst Gerontol, Res Team Social Participat & Community Hlth, Tokyo, Japan
[7] Showa Univ, Dept Pharmaceut Therapeut, Div Clin Pharm, Pharm Sch, Tokyo, Japan
[8] Tokyo Metropolitan Inst Gerontol, Res Team Promoting Independence Elderly, Tokyo, Japan
[9] Kochi Univ, Kochi Med Sch, Dept Neuropsychiat, Nankoku, Kochi, Japan
[10] Kibi Int Univ, Dept Occupat Therapy, Sch Hlth Sci & Social Welf, 8 Iga Cho, Takahashi, Okayama 7168508, Japan
[11] Natl Hosp Org, Kamo Mental Hlth Ctr, Higashihiroshima, Japan
基金
日本科学技术振兴机构;
关键词
aging; brain-derived neurotrophic factor (BDNF); DNA methylation; POSTTRAUMATIC-STRESS-DISORDER; EARLY-LIFE ADVERSITY; DNA METHYLATION; BDNF GENE; PREFRONTAL CORTEX; ADULT RATS; AGE; EXPRESSION; DEPRESSION; COMMUNITY;
D O I
10.1002/gps.4927
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
ObjectiveBrain-derived neurotrophic factor (BDNF) is involved in the pathophysiology of psychiatric disorders in adults and elderly individuals, and as a result, the DNA methylation (DNAm) of the BDNF gene in peripheral tissues including blood has been extensively examined to develop a useful biomarker for psychiatric disorders. However, studies to date have not previously investigated the effect of age on DNAm of the BDNF gene in blood. In this context, we measured DNAm of 39 CpG units in the CpG island at the promoter of exon I of the BDNF gene. MethodsWe analyzed genomic DNA from peripheral blood of 105 health Japanese women 20 to 80years of age to identify aging-associated change in DNAm of the BDNF gene. In addition, we examined the relationship between total MMSE scores, numbers of stressful life events, and serum BDNF levels on DNAm of the BDNF gene. The DNAm rate at each CpG unit was measured using a MassArray((R)) system (Agena Bioscience), and serum BDNF levels were measured by ELISA. ResultsThere was a significant correlation between DNAm and age in 13 CpGs. However, there was no significant correlation between DNAm and total MMSE scores, numbers of life events, or serum BDNF levels. ConclusionDespite the small number of subjects and the inclusion of only female subjects, our results suggest that DNAm of 13 CpGs of the BDNF gene may be an appropriate biomarker for aging and useful for predicting increased susceptibility to age-related psychiatric disorders.
引用
收藏
页码:1312 / 1318
页数:7
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