Sesso Gianluca, Bargnesi Francesca, Mutti Giulia, Berloffa Stefano, Viglione Valentina, Fantozzi Pamela, Tolomei Greta, Guccione Fulvio, Muratori Pietro, Milone Annarita, Masi Gabriele
IMT School for Advanced Studies, 55100 Lucca, Italy.
Developmental Psychiatry and Psychopharmacology Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
J Clin Med. 2024 Oct 17;13(20):6196. doi: 10.3390/jcm13206196.
: Lithium is the gold-standard treatment for Bipolar Disorder (BD) in both adults and adolescents, effectively managing mood episodes and reducing suicide risk. While its efficacy in neurotypical youth is well established, its use in adolescents with Autism Spectrum Disorder (ASD) and comorbid BD remains under-researched. Here, we present the protocol for a study aiming to evaluate the efficacy and tolerability of Extended-Release Lithium Salts in treating adolescents with BD and comorbid ASD compared to neurotypical BD patients. : This longitudinal prospective naturalistic comparative study will enroll lithium-naïve adolescents aged 12-18 with BD, with or without comorbid ASD, from the Department of Child and Adolescent Psychiatry and Psychopharmacology. Participants will be followed for six months while receiving Extended-Release Lithium Salts treatment. Primary outcomes will include mood instability, suicidality, emotional dysregulation, and aggression, assessed through a range of clinical rating scales and diagnostic tools at baseline, three months, and six months. Secondary outcomes will focus on the safety and tolerability of Extended-Release Lithium Salts, with measures including side effect ratings, physical exams, and laboratory tests. : We hypothesize that Extended-Release Lithium Salts will demonstrate non-inferiority in treating BD symptoms in adolescents with comorbid ASD compared to those without ASD. : This study is poised to fill a significant gap in the literature by providing critical data on the use of lithium for adolescents with BD and ASD. Findings will inform clinical practice and future research, potentially guiding more personalized treatment approaches for this complex and vulnerable population.
锂盐是治疗成人和青少年双相情感障碍(BD)的金标准疗法,能有效控制情绪发作并降低自杀风险。虽然其在神经发育正常的青少年中的疗效已得到充分证实,但在患有自闭症谱系障碍(ASD)且合并BD的青少年中的应用仍研究不足。在此,我们介绍一项研究方案,旨在评估缓释锂盐与神经发育正常的BD患者相比,在治疗患有BD且合并ASD的青少年中的疗效和耐受性。
这项纵向前瞻性自然主义比较研究将招募来自儿童和青少年精神病学与精神药理学部门的12 - 18岁未使用过锂盐治疗的患有BD(无论是否合并ASD)的青少年。参与者在接受缓释锂盐治疗期间将被随访六个月。主要结局将包括情绪不稳定、自杀倾向、情绪调节障碍和攻击性,通过一系列临床评定量表和诊断工具在基线、三个月和六个月时进行评估。次要结局将关注缓释锂盐的安全性和耐受性,措施包括副作用评级、体格检查和实验室检查。
我们假设,与未患ASD的青少年相比,缓释锂盐在治疗合并ASD的青少年BD症状方面将显示出非劣效性。
这项研究有望通过提供关于锂盐用于患有BD和ASD的青少年的关键数据,填补文献中的重大空白。研究结果将为临床实践和未来研究提供信息,可能为这一复杂且脆弱的人群指导更个性化的治疗方法。