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儿童发病的视神经脊髓炎谱系疾病伴水通道蛋白 4(AQP4)抗体相关的内分泌病变。

Endocrinopathies in paediatric-onset neuromyelitis optica spectrum disorder with aquaporin 4 (AQP4) antibody.

机构信息

Department of Paediatric Neurology, Great Ormond Street Hospital for Children, London, UK/Department of Neuroinflammation, Queen Square Multiple Sclerosis Centre, UCL Institute of Neurology, London, UK/Department of Neurosciences, Great Ormond Street Hospital for Children, London, UK.

Neurology Department, John Radcliffe Hospital, Oxford, UK.

出版信息

Mult Scler. 2018 Apr;24(5):679-684. doi: 10.1177/1352458517726593. Epub 2017 Aug 14.

Abstract

The involvement of the diencephalic regions in neuromyelitis optica spectrum disorder (NMOSD) may lead to endocrinopathies. In this study, we identified the following endocrinopathies in 60% (15/25) of young people with paediatric-onset aquaporin 4-Antibody (AQP4-Ab) NMOSD: morbid obesity ( n = 8), hyperinsulinaemia ( n = 5), hyperandrogenism ( n = 5), amenorrhoea ( n = 5), hyponatraemia ( n = 4), short stature ( n = 3) and central hypothyroidism ( n = 2) irrespective of hypothalamic lesions. Morbid obesity was seen in 88% (7/8) of children of Caribbean origin. As endocrinopathies were prevalent in the majority of paediatric-onset AQP4-Ab NMOSD, endocrine surveillance and in particular early aggressive weight management is required for patients with AQP4-Ab NMOSD.

摘要

脑区受累与视神经脊髓炎谱系疾病(NMOSD)有关,可能导致内分泌疾病。在这项研究中,我们在 25 名儿童起病的水通道蛋白 4 抗体(AQP4-Ab) NMOSD 患者中发现了以下内分泌疾病:病态肥胖( n = 8)、高胰岛素血症( n = 5)、高雄激素血症( n = 5)、闭经( n = 5)、低钠血症( n = 4)、身材矮小( n = 3)和中枢性甲状腺功能减退( n = 2),与下丘脑病变无关。88%(7/8)的加勒比裔儿童存在病态肥胖。由于大多数儿童起病的 AQP4-Ab NMOSD 患者都存在内分泌疾病,因此 AQP4-Ab NMOSD 患者需要进行内分泌监测,特别是早期积极的体重管理。

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