Choudhury Nuzhat, Quraishi Shamshad B, Atiqullah Akm, Khan Md Sakirul Islam, Al Mahtab Mamun, Akbar Sheikh Mf
Department of Ophthalmology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
Chemistry Division, Atomic Energy Centre, Bangladesh Atomic Energy Commission, Dhaka, Bangladesh.
Euroasian J Hepatogastroenterol. 2019 Jul-Dec;9(2):67-70. doi: 10.5005/jp-journals-10018-1299.
Chronic liver disease (CLD) is common in Bangladesh; however, a major bulk remains as cryptogenic CLD as they remain devoid of known pathological agents leading to have a check of Kayser-Fleischer (K-F) rings for possible Wilson's disease (WD) and many of these patients develop complications such as cirrhosis of liver and hepatocellular carcinoma. However, there remains considerable proportions of CLD patients with undefined etiology (cryptogenic CLD) and these patients cannot be provided effective therapy based on etiological factors. Here, the proportion of WD among cryptogenic CLD patients in Bangladesh has been evaluated to improve the management of CLD and reduce complications.
A total of 941 patients with cryptogenic CLD [negative for hepatitis viruses, alcohol, nonalcoholic fatty liver disease (NAFLD), drug, and autoimmunity] were enrolled in the study. To assess if they have been suffering from WD, the levels of copper in 24-hour urine were evaluated. Definitive WD was diagnosed when 24-hour urinary copper output was >100 μg and strongly indicative WD patients excreted >40 μg of copper in 24 hours.
Out of 941 patients with cryptogenic CLD, 212 patients were diagnosed as definitive WD and 239 patients as strongly indicative WD on the basis of 24-hours copper excretion. The age distribution ranging of the patients varied from 1 year to 90 years. There was a male predominance. Considerable numbers of WD patients had previous history of jaundice. Kayser-Fleischer rings were mostly uncommon and detected in five patients with WD only.
Wilson's disease is not a rare entity in Bangladesh; rather, it seems to be fairly common among CLD patients. A country-wide epidemiological survey should be conducted for diagnosis of WD in Bangladesh to provide a proper management strategy for these huge numbers of WD patients. In fact, most of the WD patients are unaware of their diagnosis and the general physicians are equally unaware of diagnosis and management of WD.
Choudhury N, Quraishi SB, Atiqullah AKM, . High Prevalence of Wilson's Diseases with Low Prevalence of Kayser-Fleischer Rings among Patients with Cryptogenic Chronic Liver Diseases in Bangladesh. Euroasian J Hepato-Gastroenterol 2019;9(2):67-70.
慢性肝病(CLD)在孟加拉国很常见;然而,很大一部分仍为隐源性CLD,因为它们没有已知的致病因素,因此需要检查肝豆状核变性(WD)的Kayser-Fleischer(K-F)环,而且这些患者中的许多人会出现肝硬化和肝细胞癌等并发症。然而,仍有相当比例的CLD患者病因不明(隐源性CLD),这些患者无法根据病因提供有效的治疗。在此,评估了孟加拉国隐源性CLD患者中WD的比例,以改善CLD的管理并减少并发症。
共有941例隐源性CLD患者(肝炎病毒、酒精、非酒精性脂肪性肝病(NAFLD)、药物和自身免疫检测均为阴性)纳入本研究。为评估他们是否患有WD,检测了24小时尿铜水平。当24小时尿铜排出量>100μg时诊断为确诊WD,24小时尿铜排出量>40μg为高度疑似WD患者。
在941例隐源性CLD患者中,根据24小时铜排泄量,212例患者被诊断为确诊WD,239例患者为高度疑似WD患者。患者年龄分布在1岁至90岁之间。男性居多。相当数量的WD患者既往有黄疸病史。Kayser-Fleischer环大多不常见,仅在5例WD患者中检出。
肝豆状核变性在孟加拉国并非罕见疾病;相反,在CLD患者中似乎相当常见。应在孟加拉国进行全国性的流行病学调查以诊断WD,并为大量WD患者提供适当管理策略。事实上,大多数WD患者不知道自己的病情,普通医生同样不了解WD诊断和管理。
乔杜里N,库拉希SB,阿提库拉赫AKM,等。孟加拉国隐源性慢性肝病患者中肝豆状核变性患病率高,Kayser-Fleischer环患病率低[J]。欧亚肝脏胃肠病杂志2019;9(2):67 -70。