Cell transplantation as a novel therapeutic strategy for autism spectrum disorders: a clinical study.

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2020-12-25 eCollection Date: 2020-01-01
Alok K Sharma, Nandini Gokulchandran, Pooja P Kulkarni, Hemangi M Sane, Ridhima Sharma, Alitta Jose, Prerna B Badhe
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Abstract

Background: Autism spectrum disorders [ASD] is a lifelong disability mainly affecting the development, communication, social interaction and behavior of an individual. Cell transplantation is emerging as a potential therapeutic strategy for ASD. Our previously published proof of concept study showed beneficial effects of cell transplantation in ASD. This study shows effect of cell transplantation in a larger sample size of ASD patients.

Methods: 254 patients diagnosed with ASD on DSM V criteria were enrolled in this open label non-randomized study. The intervention included intrathecal transplantation of autologous bone marrow mononuclear cells and neurorehabilitation. On mean follow up of 7.50 months, percentage analysis was performed on all symptomatic changes. Changes in outcome measures, Indian Scale for Assessment of Autism [ISAA] and Childhood Autism Rating Scale [CARS], were analyzed statistically using Wilcoxon Signed-Rank Test. Comparative analysis of Positron Emission Tomography [PET CT] scan brain, performed before and 6 months after intervention, was done in 86 patients to monitor the outcome at cellular level. Change in the standardized uptake values was statistically evaluated using T-Test [P≤0.05].

Results: Improvements were observed in eye contact, attention and concentration, hyperactivity, sitting tolerance, social interaction, stereotypical behavior, aggressiveness, communication, speech, command following and self-stimulatory behavior. Statistically significant improvement was observed in scores of ISAA and CARS after intervention. A significantly better outcome of the intervention was found in patients at younger age and with shorter duration of disease [<5 years from time of diagnosis]. 86 patients who underwent a repeat PET CT scan showed improved brain metabolism after intervention in areas which correlated to the symptomatic changes. No major procedure related adverse events were recorded. However, 5 patients, with history of seizure and abnormal EEG, had an episode of seizure which was managed using medications. Outcome of intervention in these patients was not affected by seizures as improvements were observed in them.

Conclusion: The results of this study indicate that autologous bone marrow mononuclear cells in combination with neurorehabilitation are a safe and effective treatment modality for ASD. It improves the quality of life of patients and helps them to integrate in mainstream lifestyle.

细胞移植作为一种治疗自闭症谱系障碍的新策略:临床研究。
背景:自闭症谱系障碍(Autism spectrum disorders, ASD)是一种主要影响个体发育、沟通、社会交往和行为的终身残疾。细胞移植正在成为一种潜在的治疗ASD的策略。我们之前发表的概念证明研究表明,细胞移植对ASD有有益的影响。这项研究显示了细胞移植在更大样本量的ASD患者中的效果。方法:254例符合DSM V标准诊断为ASD的患者被纳入这项开放标签非随机研究。干预包括自体骨髓单核细胞鞘内移植和神经康复。平均随访7.50个月,对所有症状变化进行百分比分析。结果测量指标印度自闭症评估量表(ISAA)和儿童自闭症评定量表(CARS)的变化采用Wilcoxon sign - rank检验进行统计学分析。对86例患者进行干预前和干预后6个月的脑正电子发射断层扫描(PET CT)对比分析,以监测细胞水平的预后。标准化摄取值的变化采用t检验进行统计学评价[P≤0.05]。结果:在眼神交流、注意力集中、多动、静坐耐受力、社会交往、刻板行为、攻击性、沟通、言语、命令服从和自我刺激行为方面均有改善。干预后ISAA和CARS评分有统计学意义的改善。结论:自体骨髓单个核细胞联合神经康复治疗是一种安全有效的治疗ASD的方式。提高患者的生活质量,帮助患者融入主流生活方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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