Methane gas in breath test is associated with non-alcoholic fatty liver disease.

IF 3.7 4区 医学 Q1 BIOCHEMICAL RESEARCH METHODS
Sanggwon An, Eui-Young Cho, Junho Hwang, Hyunseong Yang, Jungho Hwang, Kyusik Shin, Susie Jung, Bom-Taeck Kim, Kyu-Nam Kim, Wooyoung Lee
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引用次数: 0

Abstract

Although the associations between a patient's body mass index (BMI) and metabolic diseases, as well as their breath test results, have been studied, the relationship between breath hydrogen/methane levels and metabolic diseases needs to be further clarified. We aimed to investigate how the composition of exhaled breath gases relates to metabolic disorders, such as diabetes mellitus, dyslipidemia, hypertension, and nonalcoholic fatty liver disease (NAFLD), and their key risk factors. An analysis was performed using the medical records, including the lactulose breath test (LBT) data of patients who visited the Ajou University Medical Center, Suwon, Republic of Korea, between January 2016 and December 2021. The patients were grouped according to four different criteria for LBT hydrogen and methane levels. Of 441 patients, 325 (72.1%) had positive results for methane only (hydrogen < 20 parts per million [ppm] and methane ⩾ 3 ppm). BMIs and NAFLD prevalence were higher in patients with only methane positivity than in patients with hydrogen and methane positivity (hydrogen ⩾ 20 ppm and methane ⩾ 3 ppm). According to a multivariate analysis, the odds ratio of only methane positivity was 2.002 (95% confidence interval [CI]: 1.244-3.221,P= 0.004) for NAFLD. Our results demonstrate that breath methane positivity is related to NAFLD and suggest that increased methane gas on the breath tests has the potential to be an easily measurable biomarker for NAFLD diagnosis.

呼气测试中的甲烷气体与非酒精性脂肪肝有关。
虽然已经研究了身体质量指数(BMI)水平与代谢性疾病之间的关系,以及呼气测试结果与 BMI 水平之间的关系,但呼出气体中氢气/甲烷水平与代谢性疾病之间的关系仍有待进一步明确。本研究旨在探讨呼出气体的成分与代谢性疾病及其主要风险因素之间的关系。体重指数(BMI)水平升高会大大增加患代谢性疾病的风险;本研究将其纳入研究范围,以发现两者之间的关联。本研究还包括糖尿病、血脂异常、高血压和非酒精性脂肪肝(NAFLD)等代谢性疾病。 研究人员对2016年1月至2021年12月期间在大韩民国水原市安州大学医疗中心就诊的患者的医疗记录(包括乳果糖呼气试验(LBT)数据)进行了分析。受试者按照乳果糖呼气试验氢气和甲烷水平的四种不同标准分组:1)正常(N)(氢气< 20 ppm,甲烷< 3 ppm);2)仅氢气(H+)(氢气≥ 20 ppm,甲烷< 3 ppm);3)甲烷阳性(M+)(氢气< 20 ppm,甲烷≥ 3 ppm);4)甲烷和氢气阳性(M+/H+)(氢气≥ 20 ppm,甲烷≥ 3 ppm)。在 441 名受试者中,325 人(72.1%)的甲烷检测结果呈阳性(M+)。M+受试者的体重指数和非酒精性脂肪肝发病率高于氢气和甲烷阳性(H+/M+)受试者。根据多变量分析,M+ 与非酒精性脂肪肝的几率比(OR)为 2.002(95% CI:1.244-3.221,P = 0.004)。我们的研究结果表明,呼气甲烷阳性与非酒精性脂肪肝有关,并表明呼气检测中甲烷气体的增加有可能成为诊断非酒精性脂肪肝的一种易于测量的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of breath research
Journal of breath research BIOCHEMICAL RESEARCH METHODS-RESPIRATORY SYSTEM
CiteScore
7.60
自引率
21.10%
发文量
49
审稿时长
>12 weeks
期刊介绍: Journal of Breath Research is dedicated to all aspects of scientific breath research. The traditional focus is on analysis of volatile compounds and aerosols in exhaled breath for the investigation of exogenous exposures, metabolism, toxicology, health status and the diagnosis of disease and breath odours. The journal also welcomes other breath-related topics. Typical areas of interest include: Big laboratory instrumentation: describing new state-of-the-art analytical instrumentation capable of performing high-resolution discovery and targeted breath research; exploiting complex technologies drawn from other areas of biochemistry and genetics for breath research. Engineering solutions: developing new breath sampling technologies for condensate and aerosols, for chemical and optical sensors, for extraction and sample preparation methods, for automation and standardization, and for multiplex analyses to preserve the breath matrix and facilitating analytical throughput. Measure exhaled constituents (e.g. CO2, acetone, isoprene) as markers of human presence or mitigate such contaminants in enclosed environments. Human and animal in vivo studies: decoding the ''breath exposome'', implementing exposure and intervention studies, performing cross-sectional and case-control research, assaying immune and inflammatory response, and testing mammalian host response to infections and exogenous exposures to develop information directly applicable to systems biology. Studying inhalation toxicology; inhaled breath as a source of internal dose; resultant blood, breath and urinary biomarkers linked to inhalation pathway. Cellular and molecular level in vitro studies. Clinical, pharmacological and forensic applications. Mathematical, statistical and graphical data interpretation.
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