Driessens Natacha, Prasai Madhu, Alexopoulou Orsalia, De Block Christophe, Van Caenegem Eva, T'Sjoen Guy, Nobels Frank, Ghys Christophe, Vroonen Laurent, Jonas Corinne, Corvilain Bernard, Maiter Dominique
Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Department of Endocrinology, Route de Lennik, Brussels, Belgium.
Department of Endocrinology, Cliniques Universitaires Saint Luc, Brussels, Belgium.
Endocr Connect. 2023 May 12;12(6). doi: 10.1530/EC-23-0044. Print 2023 Jun 1.
Primary adrenal insufficiency (PAI) is a rare disease with an increasing prevalence, which may be complicated by life-threatening adrenal crisis (AC). Good quality epidemiological data remain scarce. We performed a Belgian survey to describe the aetiology, clinical characteristics, treatment regimens, comorbidities and frequency of AC in PAI.
A nationwide multicentre study involving 10 major university hospitals in Belgium collected data from adult patients with known PAI.
Two hundred patients were included in this survey. The median age at diagnosis was 38 years (IQR 25-48) with a higher female prevalence (F/M sex ratio = 1.53). The median disease duration was 13 years (IQR 7-25). Autoimmune disease was the most common aetiology (62.5%) followed by bilateral adrenalectomy (23.5%) and genetic variations (8.5%). The majority (96%) of patients were treated with hydrocortisone at a mean daily dose of 24.5 ± 7.0 mg, whereas 87.5% of patients also received fludrocortisone. About one-third of patients experienced one or more AC over the follow-up period, giving an incidence of 3.2 crises per 100 patient-years. There was no association between the incidence of AC and the maintenance dose of hydrocortisone. As high as 27.5% of patients were hypertensive, 17.5% had diabetes and 17.5% had a diagnosis of osteoporosis.
This study provides the first information on the management of PAI in large clinical centres in Belgium, showing an increased frequency of postsurgical PAI, a nearly normal prevalence of several comorbidities and an overall good quality of care with a low incidence of adrenal crises, compared with data from other registries.
原发性肾上腺功能不全(PAI)是一种患病率不断上升的罕见疾病,可能并发危及生命的肾上腺危象(AC)。高质量的流行病学数据仍然匮乏。我们开展了一项比利时调查,以描述PAI的病因、临床特征、治疗方案、合并症及AC的发生频率。
一项在比利时10家主要大学医院开展的全国性多中心研究收集了已知患有PAI的成年患者的数据。
本调查纳入了200例患者。诊断时的中位年龄为38岁(四分位间距25 - 48岁),女性患病率较高(女性/男性性别比 = 1.53)。中位病程为13年(四分位间距7 - 25年)。自身免疫性疾病是最常见的病因(62.5%),其次是双侧肾上腺切除术(23.5%)和基因变异(8.5%)。大多数患者(96%)接受氢化可的松治疗,平均日剂量为24.5±7.0毫克,而87.5%的患者还接受了氟氢可的松治疗。在随访期间,约三分之一的患者经历了一次或多次AC,每100患者年的发生率为3.2次危象。AC的发生率与氢化可的松的维持剂量之间无关联。高达27.5%的患者患有高血压,17.5%患有糖尿病,17.5%被诊断为骨质疏松症。
本研究提供了比利时大型临床中心PAI管理的首批信息,与其他登记处的数据相比,显示出术后PAI的发生率增加,几种合并症的患病率接近正常,整体护理质量良好,肾上腺危象发生率较低。