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Annals of Hepatology Prevalence of fibrosis and steatosis determined by transient elastography and co...
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Vol. 30. Issue S1.
Abstracts Asociación Mexicana de Hepatología (AMH) 2024
(April 2025)
Vol. 30. Issue S1.
Abstracts Asociación Mexicana de Hepatología (AMH) 2024
(April 2025)
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Prevalence of fibrosis and steatosis determined by transient elastography and controlled attenuation parameter (Fibroscan®) in diabetic patients
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Kevin S. Vázquez-Hernández1, Andres Burak-Leipuner1, Alfredo I. Servin-Caamaño2, Javier A. Romero-Bermúdez2, Laura E. Ceceña-Martínez2, José L. Pérez-Hernández1, María C. Castañeda-Aguilar3, Fátima Higuera-de la Tijera1
1 Gastroenterology, General Hospital of México Dr Eduardo Liceága, Mexico
2 Internal Medicine, General Hospital of México Dr Eduardo Liceága, Mexico
3 Clinical Nutrition, Hospital, General Hospital of México Dr Eduardo Liceága, Mexico
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Table 1. Biochemical Characteristics of the Cohort of Patients with Diabetes.
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Vol. 30. Issue S1

Abstracts Asociación Mexicana de Hepatología (AMH) 2024

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Introduction and Objectives

Globally, a higher prevalence of metabolic dysfunction-associated fatty liver disease (MAFLD) has been reported in diabetics (55.5%) compared to the general population (25%). In Mexico, there is a lack of studies on diabetes (DM2) in this subgroup. Objective: To determine the prevalence of hepatic fibrosis and steatosis determined by FibroScanâ in patients with DM2.

Materials and Patients

An observational, descriptive, cross-sectional study included patients who attended the clinic for DM2 between August 2018 and March 2024 and underwent FibroScan® to determine the absence/presence and degree of fibrosis and steatosis. Patients were excluded if they had risky alcohol consumption, hepatitis B/C, any type of previously diagnosed hepatopathy or cirrhosis, or consumption of medications other than those for metabolic syndrome (MS). Descriptive statistics were used, and the prevalence of FibroScan® determined steatosis and fibrosis was estimated.

Results

A total of 298 patients were evaluated, 195 (64.5%) women, with a mean age of 55.6±10.8 years. Of these, 284 (95.3%) agreed to undergo FibroScan® examination, none had risky alcohol consumption, 146 (51.4%) were smokers, 114 (40.1%) were overweight, 75 (25.6%) had grade I obesity, 34 (12%) had grade II obesity, and 14 (4.9%) had grade III obesity. 106 (56.3%) were hypertensive, 177 (62.3%) had dyslipidemia, and 168 (59.2%) met the criteria for MS. Regarding the FibroScan® parameters, 109 (38.4%) had steatosis: S1 in 34 (12%), S2 in 33 (11.6%), and S3 in 42 (14.8%). There was fibrosis in 155 (56.4%): F1 in 42 (14.8%), F2 in 40 (14.1%), F3 in 26 (9.2%), and F4 in 47 (16.5%). The biochemical parameters of this cohort are shown in Table 1. There was no relationship between the duration of DM2, the stage of disease control, recent adherence to treatment, and the presence or stage of steatosis or fibrosis (p=N.S.).

Conclusions

The prevalence of MASLD associated steatosis and fibrosis is high in Mexican diabetic patients and occurs independently of disease control, disease duration, and recent adherence to treatment.

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Ethical Statement: This study was conducted following the principles and ethical standards of our institution in accordance with the Declaration of Helsinki.

Declaration of Interests: None.

Funding: This project was financed through the “Young Researchers Scholarship” awarded to Dr. Kevin Sergio Vázquez Hernández by Grupo Medifarma S.A. de C.V.

Table 1.

Biochemical Characteristics of the Cohort of Patients with Diabetes.

Variable  Mean (± Standard Deviation)  Range 
Glucose (mg/dL)  129 ± 48  51 – 360 
HbA1c (%)  7.42 ± 2  4 – 16.7 
Creatinine (mg/dL)  0.88 ± 0.46  0.4 – 4.08 
Aspartate Aminotransferase (U/L)  28 ± 18.5  10 – 180 
Alanine Aminotransferase (U/L)  29.5 ± 20.3  8.8 – 139 
Gamma-glutamil transferase (U/L)  61.5 ± 79.2  9 – 508 
Body Mass Index (kg/m229.88 ± 5.07  18.88 – 48.99 
Triglycerides (mg/dL)  185.9 ± 147.8  40 – 1385 
Total Cholesterol (mg/dL)  172.42 ± 44.24  39 – 295 
High Density Lipoproteins (mg/dL)  44.56 ± 12.65  2 – 132 
Low Density Lipoproteins (mg/dL)  104.46 ± 35  22 – 230 

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