Mysore Medical College and Research Institute, Irwin Road, Bantwal, Mysore.
J Assoc Physicians India. 2022 Apr;70(4):11-12.
The patient's history is inaccurate and unreliable in diagnosis of ALD. None of laboratory test gives an unequivocal indication of Alcohol Abuse. GGT indicates Alcohol Abuse only in background of normal LFT. After the onset of liver disease due to any etiology, GGT rise parallel to ALP. Although, AST/ALT>2 is useful marker for ALD, its valid only in Steatohepatitis. The ratio may be normal in Cirrhosis. Although serum carbohydrate deficit transferrin is most specific biomarker for ALD, its an acute phase reactant, its valid only in Steatohepatitis, not in Cirrhosis. The main metabolite of ethanol is acetaldehyde which accumulates in alcoholics. Acetaldehyde binds exposed proteins which trigger immunoglobulin production.The antibodies directed against acetaldehyde adducts are predominantly IgA type.
All subjects admitted to hospital with ALD with cirrhotic dose consumption were studied. The stage of ALD was decided based on serum albumin, Ultrasound abdomen and Fibroscan. Those seronegative for Viral Hepatitis were included in the study. Serum IgA, Serum IgA/IgG ratio, serum AST/ALT ratio, serum GGT and MCV were computed and correlated using Pearson's Chi-square test and ANOVA test.
A total of 55 patients were studied. Mean age was 44 years with male preponderance of 91%. 24% were in steatosis,32% were in steatohepatitis, while 44% were in cirrhosis. Normal serum IgA upto 300 mg/dl. In this study, mean IgA in steatosis - 701 mg/dl, in steatohepatitis 1180mg/dl and cirrhosis- 1181 mg/dl. Normal serum IgA/ IgG ratio upto 0.2. In this study, this ratio in steatosis -0.3, steatohepatitis -0.5, cirrhosis- 0.6. There was significant correlation between IgA levels with advancing stages of ALD and amount of alcohol consumed. Since majority of subjects were cirrhotics where AST and ALT were normal, there was no association between AST/ALT ratio and IgA/IgG ratio. There was significant correlation between serum GGT and IgA/IgG ratio since majority were active alcoholics. Serum IgA>1200 mg/dl and IgA/IgG >0.5 correlated with onset of Hepatorenal Syndrome.
The present study shows that IgA concentration increases in all stages of ALD, while AST/ ALT ratio increase only in Steatosis/Hepatitis. Although Hypergammaglobulinemia is known to occur in CLD, the fraction of immunoglobulin elevated indicates etiology of Liver Disease. IgA is elevated fraction in ALD. Its level can be used to decide the stage of ALD and prognosis.
在诊断ALD 时,患者的病史不准确且不可靠。没有任何实验室检查能明确提示酒精滥用。GGT 仅在 LFT 正常的情况下提示酒精滥用。由于任何病因引起的肝病发作后,GGT 与 ALP 平行升高。尽管 AST/ALT>2 是 ALD 的有用标志物,但仅在脂肪性肝炎中有效。该比值在肝硬化中可能正常。尽管血清碳水化合物缺乏转铁蛋白是 ALD 最特异的生物标志物,但它是一种急性时相反应物,仅在脂肪性肝炎中有效,在肝硬化中无效。乙醇的主要代谢物是乙醛,在酗酒者中积累。乙醛与暴露的蛋白质结合,触发免疫球蛋白的产生。针对乙醛加合物的抗体主要为 IgA 型。
研究了所有因 ALD 住院且肝硬化酒精摄入量的患者。ALD 的分期根据血清白蛋白、腹部超声和 Fibroscan 确定。那些病毒性肝炎血清学阴性的患者被纳入研究。计算了血清 IgA、血清 IgA/IgG 比值、血清 AST/ALT 比值、血清 GGT 和 MCV,并使用 Pearson 卡方检验和 ANOVA 检验进行了相关性分析。
共研究了 55 例患者。平均年龄为 44 岁,男性优势为 91%。24%处于脂肪变性,32%处于脂肪性肝炎,44%处于肝硬化。正常血清 IgA 高达 300mg/dl。在这项研究中,脂肪变性组的平均 IgA 为 701mg/dl,脂肪性肝炎组为 1180mg/dl,肝硬化组为 1181mg/dl。正常血清 IgA/IgG 比值高达 0.2。在这项研究中,脂肪变性组的比值为 0.3,脂肪性肝炎组为 0.5,肝硬化组为 0.6。随着 ALD 分期的进展和饮酒量的增加,IgA 水平呈显著相关性。由于大多数患者是肝硬化,AST 和 ALT 正常,因此 AST/ALT 比值与 IgA/IgG 比值之间无相关性。由于大多数患者为活动期酗酒者,血清 GGT 与 IgA/IgG 比值之间存在显著相关性。血清 IgA>1200mg/dl 和 IgA/IgG>0.5 与肝肾综合征的发生相关。
本研究表明,在 ALD 的所有阶段,IgA 浓度均升高,而 AST/ALT 比值仅在脂肪变性/肝炎时升高。尽管已知在 CLD 中会发生高丙种球蛋白血症,但升高的免疫球蛋白片段表明肝脏疾病的病因。在 ALD 中升高的是 IgA 片段。其水平可用于决定 ALD 的分期和预后。