利用%碳水化合物缺乏转铁蛋白作为生物标志物来补充酒精依赖患者饮酒分层访谈:旨在应用于脂肪肝疾病。

IF 1.8 Q2 MEDICINE, GENERAL & INTERNAL
JMA journal Pub Date : 2025-07-15 Epub Date: 2025-06-13 DOI:10.31662/jmaj.2025-0109
Motoh Iwasa, Akiko Eguchi, Tatsuya Suzuki, Ryuta Shigefuku, Saeko Nagao, Masayuki Morikawa, Kazushi Sugimoto, Hayato Nakagawa
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引用次数: 0

摘要

酒精依赖与各种问题有关,不仅包括酒精相关/相关肝脏疾病(ALD),还包括社会孤立,因此评估酒精消耗对患者管理至关重要。与此同时,一个多社会共识小组提出了一种基于酒精消费的脂肪变性肝病(SLD)的新分类,包括ALD。酒精摄入量的评估使用诸如酒精使用障碍鉴定测试和终生饮酒史等工具;然而,这些工具在临床环境中可能缺乏准确性。碳水化合物缺乏转铁蛋白(%CDT)是酒精消耗的定量和客观的生物标志物。因此,我们的目的是确定酒精消费分层的%CDT值。方法:本横断面分析包括来自两家专业酒精依赖医疗中心住院或门诊治疗患者的285份血清样本。参与者是酒精依赖患者,他们接受了关于饮酒、血液生化测试和%CDT测试的详细访谈。结果:285份样本中,32.6%、19.6%和47.7%分别对应于男性≤30 g/天/女性≤20 g/天、男性30-60 g/天/女性20-50 g/天、男性≥60 g/天/女性≥50 g/天的酒精消费水平。%CDT值随酒精摄入量的增加而增加(p < 0.05-0.0001)。反映男性30克/天、女性20克/天和男性60克/天、女性50克/天饮酒量的临界值分别为1.67%和2.48%。γ -谷氨酰转移酶(GGT)和GGT- cdt能够区分酒精摄入量高于和低于60克/天的男性和低于50克/天的女性(p < 0.0001)。然而,他们难以区分男性每天饮酒量在30克以上和低于30克,女性每天饮酒量在20克以下。结论:%CDT与详细访谈相结合,可用于检测酒精摄入量,特别是区分男性是否超过30克/天,女性是否超过20克/天。将此应用于伴有ALD或SLD的酒精依赖患者的临床管理可能有助于提高护理质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Utilizing %Carbohydrate-deficient Transferrin as a Biomarker to Complement Interviews in Stratifying Alcohol Consumption in Patients with Alcohol Dependence: Aiming for Application to Fatty Liver Disease.

Utilizing %Carbohydrate-deficient Transferrin as a Biomarker to Complement Interviews in Stratifying Alcohol Consumption in Patients with Alcohol Dependence: Aiming for Application to Fatty Liver Disease.

Utilizing %Carbohydrate-deficient Transferrin as a Biomarker to Complement Interviews in Stratifying Alcohol Consumption in Patients with Alcohol Dependence: Aiming for Application to Fatty Liver Disease.

Utilizing %Carbohydrate-deficient Transferrin as a Biomarker to Complement Interviews in Stratifying Alcohol Consumption in Patients with Alcohol Dependence: Aiming for Application to Fatty Liver Disease.

Introduction: Alcohol dependence is linked to various issues, including not only alcohol-associated/related liver disease (ALD) but also social isolation, making the assessment of alcohol consumption crucial for patient management. Meanwhile, a multisociety consensus group has introduced a new classification for steatotic liver disease (SLD), including ALD, based on alcohol consumption. The evaluation of alcohol intake uses tools such as the Alcohol Use Disorders Identification Test and Lifetime Drinking History; however, these tools may lack accuracy in clinical settings. Carbohydrate-deficient transferrin (%CDT) is a quantitative and objective biomarker for alcohol consumption. Therefore, we aimed to determine %CDT values that stratify alcohol consumption.

Methods: This cross-sectional analysis included 285 serum samples from patients receiving inpatient or outpatient treatment at two specialized alcohol dependency medical centers. Participants were alcohol-dependent patients who underwent detailed interviews regarding alcohol consumption, biochemical blood tests, and %CDT testing.

Results: Among the 285 samples, 32.6%, 19.6%, and 47.7% corresponded to alcohol consumption levels of ≤30 g/day for men/≤20 g/day for women, 30-60 g/day for men/20-50 g/day for women, and ≥60 g/day for men/≥50 g/day for women, respectively. %CDT values increased with increasing alcohol consumption (p < 0.05-0.0001). The cutoff values reflecting alcohol consumption of 30 g/day for men/20 g/day for women and 60g/day for men/50g/day for women were 1.67% and 2.48%, respectively. Gamma-glutamyl transferase (GGT) and GGT-CDT were able to distinguish between alcohol consumption above and below 60 g/day for men and 50 g/day for women (p < 0.0001). However, they had difficulty distinguishing between alcohol consumption above and below 30 g/day for men and 20 g/day for women.

Conclusions: %CDT, in conjunction with detailed interviews, can be used to detect alcohol consumption, particularly to distinguish whether it exceeds 30 g/day in men and 20 g/day in women. Applying this to the clinical management of patients with alcohol dependence accompanied by ALD or SLD may contribute to improving the quality of care.

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