三碘甲状腺乙酸早期干预对一名 MCT8 缺乏症男孩的外周和神经发育结果的影响

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Yağmur Ünsal, Gamze Hayran
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引用次数: 0

摘要

单羧酸盐转运体8(MCT8)缺乏症是一种罕见的遗传性疾病,其特征是外周甲状腺毒症和因脑甲状腺功能减退而导致的严重认知和运动障碍。3,3',5-三碘甲状腺乙酸(Triac)可改善外周甲状腺毒症,但有关神经发育结果的数据却很少。本文介绍了一例MCT8缺乏症病例以及使用Triac治疗的经验,重点关注神经发育和外周特征的变化。五个月大的男婴因喂养困难、中枢肌张力低下和全面发育迟缓而转诊。尽管进行了六个月的物理治疗,但身体发育里程碑没有改善,远端肌张力增加。发现了SLC16A2半杂合子致病变异,确认了MCT8缺乏症。TSH为2.83 mIU/ml,游离甲状腺素:6.24pmol/L(N:12-22),游离三碘甲状腺原氨酸(FT3):15.65pmol/L(N:3.1-6.8)。他有心动过速、血压和转氨酶升高。21个月时开始服用三酰甘油。治疗两周后,FT3急剧下降,28个月时血清FT3达到稳定的正常水平。在治疗后的基线、6 个月和 12 个月,对患者的神经发育里程碑和甲状腺功能亢进症状进行了评估。6个月后,甲状腺功能亢进的症状有所改善。贝利婴儿发育量表第三版的发育综合评分保持不变,但达到了重要的发育里程碑(头部控制、认识照顾者、对自己的名字做出反应),在已达到的里程碑方面没有观察到倒退。目前正在制定 Triac 的初始剂量和管理方案,并研究其对 MCT8 缺乏症神经发育症状的疗效。本病例证实,Triac可成功缓解外周性甲状腺毒症,并可延缓神经发育的退步,同时在治疗一年后可达到某些发育里程碑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Early Intervention with Triiodothyroacetic Acid on Peripheral and Neurodevelopmental Findings in a Boy with MCT8 Deficiency

Monocarboxylate transporter 8 (MCT8) deficiency is a rare genetic disorder characterized by peripheral thyrotoxicosis and severe cognitive and motor disability due to cerebral hypothyroidism. 3,3’,5-triiodothyroacetic acid (Triac) was shown to improve peripheral thyrotoxicosis but data on neurodevelopmental outcome are scarce. We present a case of MCT8 deficiency and the experience with Triac focusing on change in neurodevelopmental and peripheral features. A five-month-old boy was referred because of feeding difficulty, central hypotonia and global developmental delay. Despite six months of physiotherapy, physical developmental milestones did not improve, and distal muscle tone was increased. A hemizygous pathogenic variant in SLC16A2 was found and MCT8 deficiency was confirmed at 19-months. Thyroid stimulating hormone was 2.83 mIU/mL, free thyroxine 6.24 pmol/L (N=12-22) and free triiodothyronine (FT3) 15.65pmol/L (N=3.1-6.8). He had tachycardia, blood pressure and transaminases were elevated. Triac was started at 21-months. Two weeks after treatment, FT3 dramatically decreased, steady normal serum FT3 was achieved at 28-months. Assessment of neurodevelopmental milestones and signs of hyperthyroidism were evaluated at baseline, 6 months and 12 months after treatment. Signs of hyperthyroidism were improved by 6 months. Developmental composite scores of Bayley Scales of Infant Developmental 3rd Edition remained the same but important developmental milestones (head control, recognition of caregiver, response to his name) were attained, regression in the attained milestones were not observed. Initial dose, management protocol for Triac and research into its efficacy on neurodevelopmental signs in MCT8 deficiency are progressing. This case presents evidence that Triac may resolve peripheral thyrotoxicosis successfully and may slow neurodevelopmental regression, while some developmental milestones were achieved after one year of treatment.

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来源期刊
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
3.60
自引率
5.30%
发文量
73
审稿时长
20 weeks
期刊介绍: The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.
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