氟西汀和舍曲林抑制青春期身高增长和生长激素信号传导

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Clinical Psychopharmacology Pub Date : 2024-11-01 Epub Date: 2024-10-14 DOI:10.1097/JCP.0000000000001922
Chadi Calarge, Chima Amushie, Stephanie Dinh, James A Mills, Sridevi Devaraj, Griselda Barba-Villalobos, Jacqueline Nguyen, Jose M Garcia, Stephanie Sisley, Fida Bacha, Babette Zemel
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引用次数: 0

摘要

目的:本研究旨在探讨氟西汀和舍曲林对青春期身高增长和胰岛素样生长因子-1(IGF-1)的影响:在这项为期 6 个月的队列研究中,研究人员利用电子病历识别了 8 至 15 岁的参与者,这些参与者在开始服用氟西汀(39 人)或舍曲林(27 人)后 1 个月内确认了性成熟 2 至 4 期。患有影响身高增长的疾病者将被排除在外。参与者接受了人体测量评估和抽血检查。未服药的健康儿童(36 人)也提供了人体测量数据:在考虑了基线身高Z-分数、性别、Tanner阶段、每日选择性5-羟色胺再摄取抑制剂(SSRI)剂量和时间后,SSRI治疗参与者的剂量与时间的交互效应与身高Z-分数成反比(β = -0.18;95%置信区间[CI]:-0.35,-0.02)。舍曲林和氟西汀对身高增长的影响没有差异。与不用药相比,SSRI 治疗与身高增长的相关性较小(时间 × 剂量的双向交互效应 β = -1.30; 95% CI: -2.52, -0.09)。剂量与时间的交互效应对体重指数 Z 值(β = 0.35;95% CI:0.06,0.64)有显著影响,但对体重 Z 值(β = 0.24;95% CI:-0.01,0.49)无显著影响。与氟西汀相比,舍曲林对体重指数 Z 值的影响更大(时间 × 剂量 × SSRI 类型的三方交互效应 P < 0.05)。SSRI剂量与IGF-1(β=-63.5;95% CI:-112.2,-14.7)成反比,但与胰岛素生长因子结合蛋白-3浓度(β=-207.3;95% CI:-536.2,121.5)无关:结论:氟西汀和舍曲林能降低身高增长和胰岛素生长因子-1浓度,其作用呈剂量依赖性。有必要进行更长期的研究。
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Fluoxetine and Sertraline Inhibit Height Growth and Growth Hormone Signaling During Puberty.

Purpose: The aim of this study was to examine the effect of fluoxetine and sertraline on height growth and insulin-like growth factor-1 (IGF-1) during puberty.

Methods: In this 6-month cohort study, electronic medical records were used to identify 8- to 15-year-old participants, within 1 month of starting fluoxetine (n = 39) or sertraline (n = 27), and sexual maturation stages 2 to 4 were confirmed. Conditions that interfere with height growth led to exclusion. Participants underwent anthropometric assessments and phlebotomy. Healthy, unmedicated children (n = 36) also provided anthropometric data.

Results: After the baseline height Z-score, sex, Tanner stage, daily selective serotonin reuptake inhibitor (SSRI) dose, and time were accounted for, the interaction effect of dose by time was inversely associated with height Z-score in SSRI-treated participants (β = -0.18; 95% confidence interval [CI]: -0.35, -0.02). Sertraline and fluoxetine did not differ in their effect on height growth. Compared with being unmedicated, SSRI treatment was associated with a smaller growth in height (time × dose 2-way interaction effect β = -1.30; 95% CI: -2.52, -0.09). The interaction effect of dose by time was significant for body mass index Z-score (β = 0.35; 95% CI: 0.06, 0.64) but not weight Z-score (β = 0.24; 95% CI: -0.01, 0.49). Body mass index Z-score increased more with sertraline compared with fluoxetine (time × dose × SSRI type 3-way interaction effect P < 0.05). SSRI dose was inversely associated with IGF-1 (β = -63.5; 95% CI: -112.2, -14.7) but not insulin growth factor binding protein-3 concentration (β = -207.3; 95% CI: -536.2, 121.5).

Conclusions: Fluoxetine and sertraline reduce height gain and IGF-1 concentration, in a dose-dependent manner. Longer-term studies are necessary.

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来源期刊
CiteScore
4.00
自引率
3.40%
发文量
231
审稿时长
4-8 weeks
期刊介绍: Journal of Clinical Psychopharmacology, a leading publication in psychopharmacology, offers a wide range of articles reporting on clinical trials and studies, side effects, drug interactions, overdose management, pharmacogenetics, pharmacokinetics, and psychiatric effects of non-psychiatric drugs. The journal keeps clinician-scientists and trainees up-to-date on the latest clinical developments in psychopharmacologic agents, presenting the extensive coverage needed to keep up with every development in this fast-growing field.
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