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DOI 10.1016/j.aohep.2024.101762

Медицинская библиотека · Annals of hepatology · 2024

Factors associated with obtaining lower IQR-CAP values in the detection of hepatic steatosis by transient elastography.

López-Mendez Iván, Romero-Flores Juan Luis, Castro-Narro Graciela, Uribe Misael, Juárez-Hernández Eva

СтатьяПеревод пока не подготовлен

Аннотация

INTRODUCTION AND

OBJECTIVES

Controlled attenuation parameter (CAP) has been developed as a non-invasive method for detecting liver steatosis. The aim of the study was to determine factors associated with non-obtaining lower IQR-CAP values.

MATERIALS AND

METHODS

Retrospective revision of medical records of CAP studies for steatosis screening. Anthropometrical, biochemical, and quality variables were collected. A logistic regression analysis was performed to determine independent associations with non-obtaining IQR-CAP <30, <20, and <10 in all patients and then adjusted for obesity/overweight and severity of steatosis.

RESULTS

5061 studies were analyzed. Median IQR-CAP was 26 [IQR 20-33] dB/m. Steatosis prevalence was 39.4 % (n = 1996). In overweight patients, significant alcohol consumption was an independent factor for non-obtaining IQR-CAP <30; meanwhile, in obese patients glucose impairment, AST, skPa>8 and steatosis severity were independent factors for non-obtaining lower IQR-CAP values. According to steatosis severity, the presence of anthropometric characteristics of obesity and significant alcohol consumption were independent factors for non-obtaining lower IQR-CAP values.

CONCLUSIONS

In steatosis detection by CAP, obesity, significant alcohol consumption, glucose impairments, and minimal liver function test alterations were independent factors associated with non-obtaining lower values of IQR-CAP.

Для цитирования: López-Mendez Iván, Romero-Flores Juan Luis, Castro-Narro Graciela, Uribe Misael, Juárez-Hernández Eva. Factors associated with obtaining lower IQR-CAP values in the detection of hepatic steatosis by transient elastography.. Annals of hepatology. 2024. DOI: 10.1016/j.aohep.2024.101762.

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