Association of telomere length and mitochondrial DNA copy number with risperidone treatment response in first-episode antipsychotic-naive schizophrenia

被引:41
|
作者
Li, Zongchang [1 ,2 ]
Hu, Maolin [1 ]
Zong, Xiaofen [1 ]
He, Ying [1 ]
Wang, Dong [1 ]
Dai, Lulin [1 ]
Dong, Min [1 ]
Zhou, Jun [1 ]
Cao, Hongbao [3 ]
Lv, Luxian [5 ]
Chen, Xiaogang [1 ,2 ,4 ]
Tang, Jinsong [1 ,3 ,4 ]
机构
[1] Cent South Univ, Key Lab Psychiat & Mental Hlth Hunan Prov, Xiangya Hosp 2, Mental Hlth Inst, Changsha 410011, Hunan, Peoples R China
[2] Cent South Univ, State Key Lab Med Genet, Changsha 410011, Hunan, Peoples R China
[3] NIMH, Unit Stat Genom, NIH, Bethesda, MD 20892 USA
[4] Natl Clin Res Ctr Psychiat & Psychol Dis, Changsha, Hunan, Peoples R China
[5] Xinxiang Med Univ, Affiliated Hosp 2, Dept Psychiat, Xinxiang, Henan, Peoples R China
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
中国国家自然科学基金;
关键词
BIPOLAR DISORDER; GENE-EXPRESSION; COMPLEX-I; LONGER; INHIBITION; STRIATUM; HISTORY; CORTEX; DAMAGE;
D O I
10.1038/srep18553
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Accumulating evidence indicates a putative association of telomere length and mitochondrial function with antipsychotics response in schizophrenia (SCZ). However, pharmacological findings were limited and no previous work has assessed this in a prospective longitudinal study. This study assessed telomere length and mitochondrial DNA copy number in first-episode antipsychotic-naive SCZ patients with 8-week risperidone treatment to evaluate the association between these biomarkers and clinical treatment response. We recruited 137 first-episode antipsychotic-naive SCZ patients (and 144 controls) at baseline and 89 patients completed the 8-week follow-up. Patients, completed follow-up, were divided into Responders (N = 46) and Non-Responders (N = 43) according to the percentage of symptoms improvement. Linear regression analyses show that SCZ patients had significantly lower mtDNA copy number (beta = -0.108, p = 0.002), and no alteration of telomere length when compared with healthy controls. In addition, compared with Non-Responders, Responders had significantly lower mtDNA copy number (beta = -0.178, p = 0.001), and longer telomere length (beta = 0.111, p = 0.071) before the 8-week treatment. After treatment, Responders persisted lower mtDNA copy number comparing with No-Responders (partial eta(2) = 0.125, p = 0.001). These findings suggest that telomere length and mtDNA copy number may hold the potential to serve as predictors of antipsychotic response of SCZ patients.
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页数:7
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