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Your search keyword '"Sheptulina, Anna F."' showing total 12 results
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12 results on '"Sheptulina, Anna F."'

1. Sonographic Features of Rectus Femoris Muscle in Patients with Metabolic Dysfunction-Associated Fatty Liver Disease and Their Correlation with Body Composition Parameters and Muscle Strength: Results of a Single-Center Cross-Sectional Study.

Author

Sheptulina, Anna F., Yafarova, Adel A., Mamutova, Elvira M., and Drapkina, Oxana M.

Subjects
RECTUS femoris muscles, DUAL-energy X-ray absorptiometry, MUSCLE strength measurement, FATTY liver, BONE density
Abstract

This study aimed to describe sonographic features of rectus femoris muscle (RFM) in patients with metabolic dysfunction-associated fatty liver disease (MASLD) and their correlation with body composition parameters and muscle strength. A total of 67 patients with MASLD underwent dual-energy X-ray absorptiometry (DEXA), bioimpedance analysis (BIA), muscle strength measurement (grip strength [GS] and chair stand test [CST]), and ultrasound (US) investigation of the RFM in the dominant thigh using a 4 to 18 MHz linear probe. MASLD patients exhibited increased RFM echogenicity, possibly due to fatty infiltration. We confirmed that the greater the subcutaneous fat thickness, the smaller was the muscle mass (p < 0.001), and the lower was the muscle strength (p < 0.001 for GS and p = 0.002 for CST). On the contrary, the greater the anteroposterior diameter (APD) of RFM, the higher was the muscle mass (p < 0.001), and the greater was the muscle strength (p < 0.001 for GS and p = 0.007 for CST). In addition, APD of the RFM and stiffness of RFM exhibited direct correlation with bone mineral density values of the lumbar spine (p = 0.005 for both GS and CST). We concluded that US investigation of the RFM in the dominant thigh can be helpful in identifying MASLD patients at a high risk of musculoskeletal disorders given repeated point-of-care clinical evaluations. [ABSTRACT FROM AUTHOR]

Published
2024
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2. Gut Microbiota Patterns in Patients with Non-Alcoholic Fatty Liver Disease: A Comprehensive Assessment Using Three Analysis Methods

Author

Korobeinikova, Anna V., primary, Zlobovskaya, Olga A., additional, Sheptulina, Anna F., additional, Ashniev, German A., additional, Bobrova, Maria M., additional, Yafarova, Adel A., additional, Akasheva, Dariga U., additional, Kabieva, Shuanat Sh., additional, Bakoev, Siroj Yu., additional, Zagaynova, Anjelica V., additional, Lukashina, Maria V., additional, Abramov, Ivan A., additional, Pokrovskaya, Mariya S., additional, Doludin, Yurii V., additional, Tolkacheva, Larisa R., additional, Kurnosov, Alexander S., additional, Zyatenkova, Elena V., additional, Lavrenova, Evgeniya A., additional, Efimova, Irina A., additional, Glazunova, Evgeniya V., additional, Kiselev, Anton R., additional, Shipulin, German A., additional, Kontsevaya, Anna V., additional, Keskinov, Anton A., additional, Yudin, Vladimir S., additional, Makarov, Valentin V., additional, Drapkina, Oxana M., additional, and Yudin, Sergey M., additional

Published
2023
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8. Diversities in the Gut Microbial Patterns in Patients with Atherosclerotic Cardiovascular Diseases and Certain Heart Failure Phenotypes

Author

Drapkina, Oxana M., primary, Ashniev, German A., additional, Zlobovskaya, Olga A., additional, Yafarova, Adel A., additional, Dementeva, Elena V., additional, Kaburova, Anastasia N., additional, Meshkov, Ivan O., additional, Sheptulina, Anna F., additional, Kiselev, Anton R., additional, Kontsevaya, Anna V., additional, Zhamalov, Linar M., additional, Koretskiy, Sergey N., additional, Pokrovskaya, Mariya S., additional, Akinshina, Alexandra I., additional, Zagaynova, Anjelica V., additional, Lukashina, Mariia V., additional, Kirillov, Andrey V., additional, Abramov, Ivan A., additional, Tolkacheva, Larisa R., additional, Bikaeva, Irina O., additional, Glazunova, Evgeniya V., additional, Shipulin, German A., additional, Bobrova, Maria M., additional, Makarov, Valentin V., additional, Keskinov, Anton A., additional, Yudin, Vladimir S., additional, and Yudin, Sergey M., additional

Published
2022
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12. Bioelectrical Impedance Analysis Demonstrates Reliable Agreement with Dual-Energy X-ray Absorptiometry in Identifying Reduced Skeletal Muscle Mass in Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease and Hypertension.

Author

Sheptulina AF, Lyusina EO, Mamutova EM, Yafarova AA, Kiselev AR, and Drapkina OM

Abstract

Background/Objectives: Body composition (BC) affects the risk of developing metabolic dysfunction-associated steatotic liver disease (MASLD) and hypertension (HTN). Currently, dual-energy X-ray absorptiometry (DEXA) is considered the gold standard for assessing BC, even though it has some limitations, including immobility, ionizing radiation, and patient weight restrictions. The aim of the study was to evaluate the correlations of BC parameters measured by bioelectrical impedance analysis (BIA) with those measured by DEXA in patients with MASLD and HTN. Methods: Overall, 78 patients with MASLD and HTN underwent the following study procedures: compilation of an anamnesis, physical examination of a patient, laboratory tests, abdominal ultrasound, BIA, DEXA, and anthropometric measurements. Results: The agreement between BIA and DEXA in diagnosing reduced skeletal muscle mass (SMM) in patients with MASLD and HTN was moderate (kappa values were 0.440 and 0.404 in males and females, respectively). Significant strong direct correlations were found between fat mass (FM) and body fat percentage measured by BIA with corresponding measurements by DEXA ( p < 0.001 for both). The area under the receiver operating characteristic curves (AUC) of SMM to body weight ratios calculated using BIA data were 0.834 and 0.929 for reduced appendicular SMM determined by DEXA in males and females with MASLD and HTN, respectively. Conclusions: In conclusion, BIA is an easy-to-use and widely available tool for assessing SMM and FM in patients with MASLD and HTN, demonstrating reliable agreement with DEXA measurement results and completely free of its limitations.

Published
2024
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