Matei V P, Purnichi T, Mihailescu A, Grigoras R
"Prof. Dr. Alexandru Obregia" Clinical Psychiatric Hospital, Psychiatry, 2 Department, Romania.
"Prof. Dr. Alexandru Obregia" Clinical Psychiatric Hospital, Neurology, Neurosurgery, Psychiatry and Child and Adolescent Psychiatry Department, Romania.
Acta Endocrinol (Buchar). 2018 Oct-Dec;14(4):483-490. doi: 10.4183/aeb.2018.483.
Atypical antipsychotics (AAs) are the first-line treatments for schizophrenia, schizoaffective disorder and bipolar disorder. However, they are now extensively utilized as off label in a myriad of diseases despite their frequently serious metabolic side-effects and hyperprolactinemia.
The purpose of our study was to observe long-term (one year) prolactin level change in first episode schizophrenia patients treated with one of the four AAs: olanzapine, quetiapine, amisulpride, ziprasidone.
This study is an analysis of the prolactin level associated with the atypical antipsychotics used in European First Episode Schizophrenia Trial (EUFEST) study.
Seventy-three first episode schizophrenia patients from the 113 patients, randomized to one of the four AAs treatment arms. Prolactin level was obtained at baseline, 6 and 12 months for all the four AAs. Analyses have been done for each antipsychotic separately for each sex.
For the male patients neither of the four antipsychotics have been associated with a statistically significant increase of prolactin level in the entire study (p>0.05). In case of the female patients, treatment with olanzapine (p=.021) and ziprasidone (p=.005) has been associated with a decrease of prolactin level in one year compared with baseline.
In both men and women, the administration of these four AAs is not associated with the increase of prolactin levels, moreover, in women's case, there is a reduction of prolactin values at administration of Olanzapine and Ziprasidone. These results are optimistic, suggesting that long term administration of these antipsychotics is safe regarding prolactin level.
非典型抗精神病药物(AAs)是治疗精神分裂症、分裂情感性障碍和双相情感障碍的一线药物。然而,尽管它们经常会产生严重的代谢副作用和高泌乳素血症,但现在却被广泛用于多种疾病的非适应症治疗。
我们研究的目的是观察用四种AAs之一(奥氮平、喹硫平、氨磺必利、齐拉西酮)治疗的首发精神分裂症患者的长期(一年)泌乳素水平变化。
本研究是对欧洲首发精神分裂症试验(EUFEST)中使用的非典型抗精神病药物相关泌乳素水平的分析。
113例患者中的73例首发精神分裂症患者被随机分配到四个AAs治疗组之一。对所有四种AAs在基线、6个月和12个月时测定泌乳素水平。对每种抗精神病药物按性别分别进行分析。
在整个研究中,对于男性患者,四种抗精神病药物均未导致泌乳素水平有统计学意义的升高(p>0.05)。对于女性患者,与基线相比,使用奥氮平(p=0.021)和齐拉西酮(p=0.005)治疗一年后泌乳素水平有所下降。
无论男性还是女性,使用这四种AAs均不会导致泌乳素水平升高,此外,对于女性患者,使用奥氮平和齐拉西酮时泌乳素值会降低。这些结果令人乐观,表明长期使用这些抗精神病药物在泌乳素水平方面是安全的。