Division of Pediatric Neurology and Developmental Medicine, Duke University Health System, 2301 Erwin Rd., Durham, NC, 27710, USA.
Divison of Gastroenterology, Department of Pediatrics, Duke University, Durham, NC, USA.
Orphanet J Rare Dis. 2020 Sep 3;15(1):231. doi: 10.1186/s13023-020-01474-w.
Alternating Hemiplegia of Childhood (AHC) is caused by mutations of the ATP1A3 gene which is expressed in brain areas that include structures controling autonomic, gastrointestinal, gut motility and GABAergic functions. We aimed to investigate, in a cohort of 44 consecutive AHC patients, two hypotheses: 1) AHC patients frequently manifest gastrointestinal, particularly motility, problems. 2) These problems are often severe and their severity correlates with neurological impairments.
41/44 (93%) exhibited gastrointestinal symptoms requiring medical attention. For these 41 patients, symptoms included constipation (66%), swallowing problems (63%), vomiting (63%), anorexia (46%), diarrhea (44%), nausea (37%), and abdominal pain (22%). Symptoms indicative of dysmotility occurred in 33 (80%). The most common diagnoses were oropharyngeal dysphagia (63%) and gastroesophageal reflux (63%). 16 (39%) required gastrostomy and two fundoplication. Severity of gastrointestinal symptoms correlated with non-paroxysmal neurological disability index, Gross Motor Function Classification System scores, and with the presence/absence of non-gastrointestinal autonomic dysfunction (p = 0.031, 0.043, Spearman correlations and 0.0166 Cramer's V, respectively) but not with the paroxysmal disability index (p = 0.408).
Most AHC patients have gastrointestinal problems. These are usually severe, most commonly are indicative of dysmotility, often require surgical therapies, and their severity correlates with that of non-paroxysmal CNS manifestations. Our findings should help in management-anticipatory guidance of AHC patients. Furthermore, they are consistent with current understandings of the pathophysiology of AHC and of gastrointestinal dysmotility, both of which involve autonomic and GABAergic dysfunction.
儿童交替性偏瘫(AHC)是由 ATP1A3 基因突变引起的,该基因在控制自主神经、胃肠道、肠道运动和 GABA 能功能的脑区表达。我们旨在研究 44 例连续 AHC 患者的两个假设:1)AHC 患者经常出现胃肠道,特别是运动问题。2)这些问题通常很严重,其严重程度与神经功能障碍相关。
44 例中有 41 例(93%)出现需要医疗关注的胃肠道症状。对于这 41 例患者,症状包括便秘(66%)、吞咽问题(63%)、呕吐(63%)、食欲不振(46%)、腹泻(44%)、恶心(37%)和腹痛(22%)。表明存在运动障碍的症状发生在 33 例(80%)。最常见的诊断是口咽吞咽困难(63%)和胃食管反流(63%)。16 例(39%)需要胃造口术,2 例需要胃底折叠术。胃肠道症状的严重程度与非阵发性神经功能障碍指数、粗大运动功能分类系统评分以及是否存在/不存在非胃肠道自主神经功能障碍相关(p=0.031、0.043、Spearman 相关性和 0.0166 Cramer's V,分别),但与阵发性残疾指数无关(p=0.408)。
大多数 AHC 患者存在胃肠道问题。这些问题通常很严重,最常见的是运动障碍,经常需要手术治疗,其严重程度与非阵发性中枢神经系统表现相关。我们的发现有助于 AHC 患者的管理-预测性指导。此外,它们与 AHC 和胃肠道运动障碍的病理生理学的当前理解一致,这两者都涉及自主神经和 GABA 能功能障碍。