Serum Neudesin Levels in Patients with Congenital Hypothyroidism

IF 1.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Clinical Research in Pediatric Endocrinology Pub Date : 2025-08-22 Epub Date: 2025-01-24 DOI:10.4274/jcrpe.galenos.2025.2024-1-14
Semra Bahar, İlker Tolga Özgen, Yaşar Cesur, Caner Yıldız, Ömer Faruk Özer, Emel Hatun Aytaç Kaplan, Zümrüt Kocabey Sütçü
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Abstract

Objective: Neudesin is a newly discovered protein mainly secreted from adipose tissue and the brain. It plays a role as a neurotrophic factor in the brain and a negative regulator of energy expenditure. Neurodevelopmental delay and cognitive dysfunction are common features in cases with congenital hypothyroidism (CH) without treatment. Given the role of neudesin in brain development and its contribution to the survival of mature neurons, the relationship between neudesin and thyroid hormone was evaluated in babies diagnosed with CH.

Methods: Babies aged between 2-4 weeks and diagnosed with CH and healthy controls of similar age were included. All patients were evaluated for thyroid hormones and plasma neudesin levels. The basal neudesin levels between the patient and control groups and the patients’ neudesin levels before and after l-thyroxine treatment were compared.

Results: Fifty-two babies [32 with CH, 14 (44%) female, aged 19±7 days and 20 healthy controls, 7 (35%) female, aged 22±8 days] were included. There was no significant difference in baseline neudesin between the CH and control groups (6.77±6.41 vs. 7.93±7.04 ng/mL, respectively; p=0.552). However, neudesin levels increased significantly following one month of therapy in the CH group [median: 3.93 (minimum: 0.31, maximum: 30.06) vs. median: 6.15 (minimum: 2.17, maximum: 70.05) ng/mL, p=0.019].

Conclusion: Although there was no difference in baseline neudesin levels between the patient and control groups, neudesin levels increased after short-term treatment. Larger prospective studies are needed to understand the pathophysiological role of neudesin in untreated and treated early CH.

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先天性甲状腺功能减退症患者血清Neudesin水平。
目的:Neudesin是一种新发现的主要由脂肪组织和大脑分泌的蛋白质。它在大脑中扮演着神经营养因子的角色,是能量消耗的负调节因子。神经发育迟缓和认知功能障碍是未经治疗的先天性甲状腺功能减退症(CH)的常见特征。考虑到neudesin在大脑发育中的作用及其对成熟神经元存活的贡献,neudesin和甲状腺激素之间可能存在的关系被评估。方法:共52例患者,其中ch32例,女14例,男18例,年龄19±7天;健康受试者20例为对照组;女性7例,男性13例,年龄22±8天。评估所有患者的甲状腺激素和血浆neudesin水平。比较患者与对照组基础neudin水平及l-甲状腺素治疗前后neudin水平。结果:CH组与对照组基础neudesin水平(6.77±6.41 vs 7.93±7.04 ng/mL)差异无统计学意义(p=0.552)。然而,治疗1个月后,CH组neudesin水平升高(6.46±6.63 vs 12.85±18.74 ng/mL);差异有统计学意义(p=0.019)。结论:虽然患者与对照组之间的基础neudesin水平没有差异,但neudesin水平随着治疗而升高。然而,需要更广泛和不同的研究来了解这种关系在疾病或恢复过程中的病理生理作用。
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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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