Can clinical parameters of patients, sans serum prolactin measurement, identify amenorrhea associated with risperidone use? Results from a cross-sectional analytical study

Vigneshvar Chandrasekaran, Avin Muthuramalingam, Karthick Subramanian
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Abstract

Background: Risperidone is a second-generation antipsychotic, which exerts its action by antagonizing dopamine (D2) and serotonin (5-HT2A) receptors. Amenorrhea is a common adverse effect observed in risperidone. Risperidone blocks the dopamine receptor of lactotroph cells of the pituitary gland, resulting in loss of the inhibitory effect of dopamine on prolactin. The resultant hyperprolactinemia decreases estrogen through its impact on the pulsatile secretion of gonadotropins and ovarian follicular growth leading to amenorrhea. Identifying the associated clinical parameters will aid in predicting the occurrence of amenorrhea in patients on treatment with risperidone, especially in a setting devoid of prolactin estimation. The objective of this study was to compare the clinical profile of patients with and without risperidone-induced amenorrhea. Methodology: A cross-sectional comparative study was done in a tertiary care hospital. A total of 30 female patients on risperidone who developed amenorrhea were recruited, and age-matched patients on risperidone without amenorrhea were taken as controls. The clinical parameters of the groups were compared using the Mann–Whitney U-test. Binary logistic regression was used to predict the clinical predictors associated with risperidone-induced amenorrhea. Results: The amenorrhea group had a significantly longer duration of untreated psychosis (DUP) (P = 0.011), duration of total treatment (P = 0.003), and duration of treatment exclusively with risperidone (P = 0.002). No significant differences were noted in the dose of risperidone (P = 0.570) and the diagnosis (P = 0.455) between the groups. However, the regression test did not confer any risk due to any clinical parameters. Conclusion: Individuals who developed amenorrhea had a longer DUP and a longer duration of treatment exclusively with risperidone.
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无血清催乳素测定的患者临床参数能否识别与利培酮使用相关的闭经?横断面分析研究的结果
背景:利培酮是第二代抗精神病药,通过拮抗多巴胺(D2)和血清素(5-HT2A)受体发挥作用。闭经是利培酮常见的不良反应。利培酮阻断脑垂体乳营养细胞的多巴胺受体,导致多巴胺对催乳素的抑制作用丧失。由此产生的高催乳素血症通过影响促性腺激素的搏动分泌和卵巢卵泡生长而导致闭经,从而降低雌激素。确定相关的临床参数将有助于预测利培酮治疗患者闭经的发生,特别是在缺乏催乳素估计的情况下。本研究的目的是比较利培酮致闭经患者和非利培酮致闭经患者的临床情况。方法:在一家三级保健医院进行横断面比较研究。共招募30例女性利培酮闭经患者,并以年龄匹配的利培酮非闭经患者为对照。采用Mann-Whitney u检验比较两组临床参数。采用二元logistic回归预测与利培酮致闭经相关的临床预测因素。结果:闭经组精神病未治疗持续时间(DUP) (P = 0.011)、总治疗持续时间(P = 0.003)、利培酮单药治疗持续时间(P = 0.002)明显延长。两组间利培酮剂量(P = 0.570)和诊断率(P = 0.455)差异无统计学意义。然而,回归测试没有由于任何临床参数而赋予任何风险。结论:闭经患者的DUP较长,利培酮治疗的持续时间较长。
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