Nakamura-Utsunomiya Akari, Hiyama Takeshi Y, Okada Satoshi, Noda Masaharu, Kobayashi Masao
Department of Pediatrics, Hiroshima University Hospital, Hiroshima, Japan.
Division of Molecular Neurobiology, National Institute for Basic Biology (NIBB), Aichi, Japan.
Clin Pediatr Endocrinol. 2017;26(4):197-205. doi: 10.1297/cpe.26.197. Epub 2017 Sep 28.
Adipsic hypernatremia is a rare disease presenting as persistent hypernatremia with disturbance of thirst regulation and hypothalamic dysfunction. As a result of congenital disease, tumors, or inflammation, most cases are accompanied by structural abnormalities in the hypothalamic-pituitary area. While cases with no hypothalamic-pituitary structural lesion have been reported, their etiology has not been elucidated. Recently, we reported three patients with adipsic hypernatremia whose serum-derived immunoglobulin (Ig) specifically reacted with mouse subfornical organ (SFO) tissue. As one of the circumventricular organs (CVOs) that form a sensory interface between the blood and brain, the SFO is a critical site for generating physiological responses to dehydration and hypernatremia. Intravenous injection of the patient's Ig fraction induced hypernatremia in mice, along with inflammation and apoptosis in the SFO. These results support a new autoimmunity-related mechanism for inducing adipsic hypernatremia without demonstrable hypothalamic-pituitary structural lesions. In this review, we aim to highlight the characteristic clinical features of these patients, in addition to etiological mechanisms related to SFO function. These findings may be useful for diagnosing adipsic hypernatremia caused by an autoimmune response to the SFO, and support development of new strategies for prevention and treatment.
无渴感高钠血症是一种罕见疾病,表现为持续性高钠血症,伴有口渴调节障碍和下丘脑功能障碍。由于先天性疾病、肿瘤或炎症,大多数病例伴有下丘脑 - 垂体区域的结构异常。虽然已报道无下丘脑 - 垂体结构病变的病例,但其病因尚未阐明。最近,我们报告了三例无渴感高钠血症患者,其血清衍生的免疫球蛋白(Ig)与小鼠穹窿下器(SFO)组织发生特异性反应。作为形成血液与大脑之间感觉界面的室周器官(CVO)之一,SFO是产生对脱水和高钠血症生理反应的关键部位。静脉注射患者的Ig组分可诱导小鼠出现高钠血症,同时伴有SFO的炎症和细胞凋亡。这些结果支持了一种新的自身免疫相关机制,可在无明显下丘脑 - 垂体结构病变的情况下诱发无渴感高钠血症。在本综述中,除了与SFO功能相关的病因机制外,我们旨在突出这些患者的特征性临床特征。这些发现可能有助于诊断由对SFO的自身免疫反应引起的无渴感高钠血症,并支持预防和治疗新策略的开发。