Singh Arun K, Jhalani Manoj, Shahi Sunil K, Christopher Rita, Kumar Bhartendu, Das Manoja K
Neonatology, All India Institute of Medical Sciences, Jodhpur, Jodhpur, IND.
National Health Mission, Ministry of Health and Family Welfare, Government of India, New Delhi, IND.
Cureus. 2023 Apr 3;15(4):e37073. doi: 10.7759/cureus.37073. eCollection 2023 Apr.
Periodic outbreaks of acute encephalopathy in children have been reported from Muzaffarpur, Bihar, India. No infectious cause has been identified for this. This study presents the clinical and metabolic profile of children hospitalized with acute encephalopathy and the potential role of ambient heat stress.
This cross-sectional study included children (<15 years) with acute encephalopathy admitted from April 4, 2019, to July 4, 2019. The clinical and laboratory investigations included infections, metabolic abnormalities, and muscle tissue analysis. The children who had metabolic derangements but no infectious cause were labeled as acute metabolic encephalopathy. The descriptive analysis summarized the clinical, laboratory, and histopathology findings, and their association with the ambient heat parameters was explored.
Out of the 450 children hospitalized (median age, four years), 94 (20.9%) died. Children had early morning onset (89%), seizures (99%), fever (82%), hypoglycemia at admission (64%), raised aminotransferases (60%), and high blood urea (66%). Blood lactate (50%), lactate dehydrogenase (84%), pyruvate (100%), ammonia (32%), and creatinine phosphokinase (69%) were raised. Viral marker tests were negative. The patients had abnormal metabolic markers like decreased blood-free carnitine, elevated blood acylcarnitines, and elevated urinary lactate, oxalate, maleate, adipate, and fatty acid metabolites. Blood carnitine and acylcarnitine levels normalized in 75% of the patients treated with carnitine and coenzyme-Q. Muscle tissues showed megamitochondria on electron microscopy and reduced respiratory enzyme complex-I activity. A significant correlation between the number of admissions and ambient heat indices was observed.
The findings suggest secondary mitochondrial dysfunction as a possible mechanism for acute encephalopathy in children from Muzaffarpur, Bihar, and ambient heat stress as a possible risk factor.
印度比哈尔邦穆扎法尔布尔地区曾报告儿童周期性急性脑病疫情。尚未确定其感染病因。本研究展示了急性脑病住院儿童的临床和代谢特征,以及环境热应激的潜在作用。
这项横断面研究纳入了2019年4月4日至2019年7月4日收治的急性脑病儿童(<15岁)。临床和实验室检查包括感染、代谢异常和肌肉组织分析。将有代谢紊乱但无感染病因的儿童标记为急性代谢性脑病。描述性分析总结了临床、实验室和组织病理学发现,并探讨了它们与环境热参数的关联。
450名住院儿童(中位年龄4岁)中,94名(20.9%)死亡。儿童发病于清晨(89%),有癫痫发作(99%)、发热(82%)、入院时低血糖(64%)、转氨酶升高(60%)和血尿素升高(66%)。血乳酸(50%)、乳酸脱氢酶(84%)、丙酮酸(100%)、氨(32%)和肌酸磷酸激酶(69%)升高。病毒标志物检测呈阴性。患者有异常代谢标志物,如血游离肉碱降低、血酰基肉碱升高以及尿乳酸、草酸盐、马来酸盐、己二酸盐和脂肪酸代谢物升高。75%接受肉碱和辅酶Q治疗的患者血肉碱和酰基肉碱水平恢复正常。肌肉组织在电子显微镜下显示有巨型线粒体,呼吸酶复合体I活性降低。观察到入院人数与环境热指数之间存在显著相关性。
研究结果表明,继发性线粒体功能障碍可能是印度比哈尔邦穆扎法尔布尔地区儿童急性脑病的发病机制,环境热应激可能是一个危险因素。