Diagnostics and treatment of non-alcoholic fatty liver disease with concomitant asthenic syndrome

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Abstract

Aim. Analysis of the effectiveness of therapy for non-alcoholic fatty liver disease (NAFLD) with severe asthenic syndrome.

Materials and methods. In the period from 2017 to 2019, on the basis of the gastroenterology center of the Vishnevsky 3-rd Central Military Clinical Hospital, 247 patients with NAFLD, including those at the stage of steatohepatitis, and severe asthenic syndrome were examined and treated. The main group included 124 patients, the control group – 123 patients. All patients underwent complex laboratory and instrumental diagnostics and neuropsychological research using the subjective asthenia assessment scale (MFI-20). In both groups, domestic drugs were included in the therapy regimen: from the 1st to the 10th day, Heptrong solution 3 ml intramuscularly in the morning; from the 1st to the 60th day – UDCA 250 mg orally, 3 capsules at bedtime, Omega-3 forte 1000 mg, 2 capsules in the morning with meals. In group I patients received additionally – from the 1st to the 10th day intravenous drip Cytoflavin 10 ml + 0.9% NaCl solution 200 ml; pentoxifylline solution 5 ml + 0.9% NaCl solution 200 ml. Then, from the 11th to the 60th day, Cytoflavin inside, 2 tablets 2 times a day. Pentoxifylline inside 400 mg 1 tablet 3 times a day. All patients underwent neuropsychological examination using the subjective asthenia rating scale (MFI-20).

Results. The effectiveness of treatment in patients of both groups was assessed by clinical, laboratory data and neuropsychological studies. In the main group, a significant reduction in asthenic syndrome was achieved against the background of diagnosed NAFLD compared with the control group.

Conclusion. The early inclusion of patients with NAFLD and severe asthenic syndrome in the treatment regimen, in addition to the basic therapy of Cytoflavin, achieved a significantly high therapeutic effect in the form of normalization of the main clinical, laboratory and instrumental parameters, as well as a significant reduction in the manifestations of asthenia.

About the authors

Aleksandr I. Pavlov

Vishnevsky 3-rd Central Military Clinical Hospital

Email: Angel2503@inbox.ru
ORCID iD: 0000-0003-1836-7946

доктор медицинских наук, доцент, начальник Центра гастроэнтерологии и гепатологии, главный гастроэнтеролог 

Russian Federation, Krasnogorsk

Aleksandr F. Ivolgin

Vishnevsky 3-rd Central Military Clinical Hospital

Email: Angel2503@inbox.ru
ORCID iD: 0000-0002-8849-680X

начальник неврологического центра, главный невролог

Russian Federation, Krasnogorsk

Sergei V. Katenko

Vishnevsky 3-rd Central Military Clinical Hospital

Email: Angel2503@inbox.ru

врач консультант-психотерапевт

Russian Federation, Krasnogorsk

Mikhail N. Eremin

Yevdokimov Moscow State University of Medicine and Dentistry

Email: Angel2503@inbox.ru
ORCID iD: 0000-0002-8798-5011

кандидат медицинских наук, ассистент кафедры пропедевтики внутренних болезней и гастроэнтерологии

Russian Federation, Moscow

Alevtina I. Molodova

Vishnevsky 3-rd Central Military Clinical Hospital

Author for correspondence.
Email: Angel2503@inbox.ru
ORCID iD: 0000-0003-3302-6541

старший лаборант каф. пропедевтики внутренних болезней и гастроэнтерологии

Russian Federation, Krasnogorsk

Olga B. Levchenko

Yevdokimov Moscow State University of Medicine and Dentistry

Email: Angel2503@inbox.ru
ORCID iD: 0000-0002-6594-7006

ассистент кафедры пропедевтики внутренних болезней и гастроэнтерологии

Russian Federation, Moscow

Aram G. Karakozov

Yevdokimov Moscow State University of Medicine and Dentistry

Email: Angel2503@inbox.ru
ORCID iD: 0000-0002-3196-4457

доктор медицинских наук, профессор, профессор каф. пропедевтики внутренних болезней и гастроэнтерологии

Russian Federation, Moscow

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Study design.

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3. Fig. 2.1. The dynamics of the indices of the general blood analysis (group 1, the main group).

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4. Fig. 2.2. The dynamics of the indices of the general blood analysis (group 2 – control).

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5. Fig. 3.1. Changes in biochemical blood count (group 1 – baseline).

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6. Fig. 3.2. Dynamics of biochemical blood count (group 2 – control).

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7. Fig. 4. Dynamics of oblique vertical dimension parameters of the right lobe of the liver according to ultrasound examination (cm).

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8. Fig. 5. The dynamics of non-alcoholic fatty liver disease ultrasound signs against the background of treatment, n (%).

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9. Fig. 6. Data on liver puncture biopsy in patients with non-alcoholic fatty liver disease, n (%).

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10. Fig. 7.1. Downward trend of MFI-20 subscale scores in group 1 (12 points are marked in red).

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11. Fig. 7.2. Evolution of MFI-20 subscale score reduction in group 2 (12 points drawn in red).

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12. Fig. 8. Comparison of the dynamics of MFI-20 subscale score reduction in group 1 and group 2.

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13. Fig. 9.1. Evolution of MFI-20 subscale score reduction and total MFI-20 score reduction in group 1.

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14. Fig. 9.2. Evolution of MFI-20 subscale scores and total MFI-20 scores in group 2.

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