Distinguishing clinical features of paediatric autoimmune Addison's disease and polyendocrine syndromes: a 15-year single-centre observational study from Baghdad, Iraq.

Q3 Medicine
Muneera Fadhil Ridha, Bayar Abdullah Ahmed, Wassan Nori
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Abstract

Introduction: Autoimmune Addison's disease (AAD) is a rare endocrine disorder characterised by immune-mediated destruction of the adrenal cortex. AAD may occur in isolation or as part of a broader autoimmune polyendocrine syndrome (APS). Distinguishing the two is essential owing to implications for patient screening and prognosis. Earlier identification of APS patients is crucial for preserving residual adrenal function and developing future targeted therapies. This study aimed to define clinical and laboratory features of paediatric isolated AAD and APS.

Material and methods: This retrospective cohort study recruited 55 paediatric patients; 27/55 had isolated AAD and 28/55 had APS. They were followed at the Children's Welfare Teaching Hospital, Baghdad, Iraq, between 2009 and 2024. Data collected and compared included: demographic variables (age, gender, family history, duration of symptoms), presenting clinical features and adrenal crisis, and laboratory parameters.

Results: Male predominance was observed in both groups, although the difference was not significant. Positive family history was more frequent in APS (p = 0.03). Clinically, hyperpigmentation, weight loss, poor appetite, and hypoglycaemia-induced seizures were significantly higher in isolated AAD (p = 0.0001, 0.0002, 0.042, 0.041). Adrenal crises were more frequent in APS cases (p = 0.18). Major risk factors for adrenal crisis included poor treatment compliance and infections. Laboratory parameters showed that hyperkalaemia and hypoglycaemia were significantly more pronounced in AAD (0.0079 and 0.00002).

Conclusions: Distinguishing isolated AAD from APS may be clinically useful. Differences were observed in metabolic severity, family history, weight loss, hyperpigmentation, and risk of adrenal crisis. These findings suggest that management of both conditions may benefit from a tailored approach, emphasizing treatment adherence and infection prevention in both groups.

区分儿童自身免疫性阿狄森病和多内分泌综合征的临床特征:一项来自伊拉克巴格达的15年单中心观察研究
自身免疫性艾迪生病(AAD)是一种罕见的内分泌疾病,其特征是免疫介导的肾上腺皮质破坏。AAD可以单独发生,也可以作为更广泛的自身免疫性多内分泌综合征(APS)的一部分。由于对患者筛查和预后的影响,区分两者是必不可少的。早期识别APS患者对于保留残余肾上腺功能和开发未来的靶向治疗至关重要。本研究旨在确定小儿孤立性AAD和APS的临床和实验室特征。材料和方法:本回顾性队列研究招募了55例儿科患者;27/55为孤立性AAD, 28/55为APS。2009年至2024年间,他们在伊拉克巴格达的儿童福利教学医院接受了随访。收集和比较的数据包括:人口统计学变量(年龄、性别、家族史、症状持续时间)、临床表现特征和肾上腺危机以及实验室参数。结果:两组患者均有男性优势,但差异不显著。阳性家族史在APS患者中更为常见(p = 0.03)。临床中,单独AAD患者色素沉着、体重减轻、食欲不振和低血糖诱发癫痫发作的发生率显著高于对照组(p = 0.0001、0.0002、0.042、0.041)。肾上腺危象在APS患者中更为常见(p = 0.18)。肾上腺危机的主要危险因素包括治疗依从性差和感染。实验室参数显示,高钾血症和低血糖在AAD中更为明显(0.0079和0.00002)。结论:区分孤立性AAD与APS可能具有临床价值。在代谢严重程度、家族史、体重减轻、色素沉着和肾上腺危机风险方面观察到差异。这些发现表明,这两种情况的管理可能受益于量身定制的方法,强调治疗依从性和感染预防两组。
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来源期刊
Pediatric Endocrinology, Diabetes and Metabolism
Pediatric Endocrinology, Diabetes and Metabolism Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.00
自引率
0.00%
发文量
36
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