Song Xueqin, Fan Xiaoduo, Li Xue, Zhang Wei, Gao Jinsong, Zhao Jingping, Harrington Amy, Ziedonis Douglas, Lv Luxian
The First Affiliated Hospital/Zhengzhou University, Zhengzhou, China, 450052,
Psychopharmacology (Berl). 2014 Jan;231(2):319-25. doi: 10.1007/s00213-013-3382-4. Epub 2013 Dec 14.
The present study aimed to examine the changes in pro-inflammatory cytokines and body weight during 6-month risperidone treatment in drug naïve, first-episode schizophrenia.
Sixty-two drug naïve, first-episode schizophrenia (SZ group) and 60 healthy individuals (control group) were enrolled in the study. Serum interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) levels, and body weight were measured at baseline for both groups, and repeated for the SZ group at five different time points during 6-month risperidone treatment.
At baseline, serum IL-1β, IL-6, and TNF-α levels in the SZ group (53.28 ± 12.62, 33.98 ± 14.13, 50.08 ± 12.86 pg/mL, respectively) were significantly higher than those in the control group (23.49 ± 15.27, 15.53 ± 7.16, 32.12 ± 15.23 pg/mL, respectively) (p's < 0.001). Within the SZ group, serum IL-1β levels decreased significantly at 2 weeks (48.02 ± 16.00 pg/mL, p < 0.01) and 1 month (44.70 ± 16.63 pg/mL, p < 0.001), but then gradually increased at 2 months (48.49 ± 18.87 pg/mL), 3 months (50.59 ± 18.48 pg/mL) and 6 months (53.64 ± 16.22 pg/mL) to the levels comparable to baseline; serum IL-6 levels changed significantly over the course of treatment (p = 0.001), but reached the levels comparable to baseline at 6 months (37.13 ± 13.23 pg/mL); serum levels of TNF-α increased significantly at 3 months (55.02 ± 16.69 pg/mL, p < 0.01) and 6 months (58.69 ± 13.57 pg/mL, p < 0.001); steady and significant weight gain was observed at each follow-up time point (p's < 0.001), from 56.71 ± 9.25 kg at baseline to 62.72 ± 9.53 kg at 6 months.
Risperidone treatment is associated with changes in serum pro-inflammatory cytokines levels and weight. There is an initial anti-inflammatory effect that reduces with treatment, potentially due to its weight gain side effect.
本研究旨在探讨初发、未用药的精神分裂症患者在接受6个月利培酮治疗期间促炎细胞因子和体重的变化。
62例初发、未用药的精神分裂症患者(精神分裂症组)和60例健康个体(对照组)纳入本研究。两组在基线时均测量血清白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)水平及体重,精神分裂症组在6个月利培酮治疗期间的5个不同时间点重复测量。
基线时,精神分裂症组血清IL-1β、IL-6和TNF-α水平(分别为53.28±12.62、33.98±14.13、50.08±12.86 pg/mL)显著高于对照组(分别为23.49±15.27、15.53±7.16、32.12±15.23 pg/mL)(p值均<0.001)。在精神分裂症组中,血清IL-1β水平在2周时(48.02±16.00 pg/mL,p<0.01)和1个月时(44.70±16.63 pg/mL,p<0.001)显著下降,但随后在2个月时(48.49±18.87 pg/mL)、3个月时(50.59±18.48 pg/mL)和6个月时(53.64±16.22 pg/mL)逐渐升高至与基线相当的水平;血清IL-6水平在治疗过程中变化显著(p=0.001),但在6个月时达到与基线相当的水平(37.13±13.23 pg/mL);血清TNF-α水平在3个月时(55.02±16.69 pg/mL,p<0.01)和6个月时(58.69±13.57 pg/mL,p<0.001)显著升高;在每个随访时间点均观察到体重稳定且显著增加(p值均<0.001),从基线时的56.71±9.25 kg增加至6个月时的62.72±9.53 kg。
利培酮治疗与血清促炎细胞因子水平和体重变化有关。存在初始抗炎作用,但随着治疗会减弱,这可能归因于其体重增加的副作用。