A case of using specialized medical nutrition product containing anhydrous betaine in patient with homocystinuria
- 作者: Agafonova A.A.1, Mikhaylova S.V.2, Votyakova N.A.2, Zazhivikhina M.V.2, Minaycheva L.I.1, Seitova G.N.2
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隶属关系:
- Tomsk National Research Medical Center
- Russian Children’s Clinical Hospital
- 期: 卷 6, 编号 1 (2025)
- 页面: 43-50
- 栏目: Case reports
- URL: https://journals.rcsi.science/2658-4433/article/view/348394
- DOI: https://doi.org/10.17816/clinutr686633
- EDN: https://elibrary.ru/PAJNTQ
- ID: 348394
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BACKGROUND: Although homocystinuria is a rare disorder, its management remains an important issue in modern pediatrics. Diet therapy is the main pathogenetic treatment for patients with homocystinuria. The use of betaine as part of combination therapy helps reduce plasma homocysteine concentrations, particularly in patients who do not respond to other treatment approaches.
A CASE REPORT: A 12-year-old child with genetically confirmed pyridoxine-responsive homocystinuria underwent substitution of an imported preparation containing anhydrous betaine with a specialized medical nutrition product, Amino Acid Module Betaine (ORPHANIC® trademark). The previously effective combination therapy regimen remained unchanged.
CONCLUSION: Replacement of anhydrous betaine within the previously established treatment regimen, followed by 30 days of administration of the medical nutrition product Amino Acid Module Betaine (ORPHANIC® trademark) containing betaine anhydrous, demonstrated a good safety profile. This substitution did not significantly affect the patient’s general condition, disease course, or key parameters of sulfur-containing amino acid metabolism.
Prescription of the medical nutrition product Amino Acid Module Betaine (ORPHANIC® trademark) containing anhydrous betaine, or transition of a patient to this product, requires monitoring of the patient’s general condition and regular determination of sulfur-containing amino acid metabolism parameters. This study represents the first clinical evaluation of anhydrous betaine produced in Russia. The obtained results indicate its efficacy and safety in the treatment of a patient with homocystinuria.
作者简介
Anna Agafonova
Tomsk National Research Medical Center
编辑信件的主要联系方式.
Email: anna.agafonova@medgenetics.ru
ORCID iD: 0009-0001-2797-2737
SPIN 代码: 8596-9192
MD
俄罗斯联邦, 3 Moskovsky Trakt, Tomsk, 634050Svetlana Mikhaylova
Russian Children’s Clinical Hospital
Email: svetychvital@mail.ru
ORCID iD: 0000-0002-2115-985X
MD, Dr. Sci. (Medicine)
俄罗斯联邦, MoscowNatalya Votyakova
Russian Children’s Clinical Hospital
Email: voina-86@mail.ru
ORCID iD: 0009-0007-4734-6526
MD
俄罗斯联邦, MoscowMayya Zazhivikhina
Russian Children’s Clinical Hospital
Email: maya2690@gmail.com
ORCID iD: 0000-0002-7595-9860
MD
俄罗斯联邦, MoscowLarisa Minaycheva
Tomsk National Research Medical Center
Email: larisa.minaycheva@medgenetics.ru
ORCID iD: 0000-0002-1752-2521
SPIN 代码: 4638-7372
MD, Dr. Sci. (Medicine)
俄罗斯联邦, TomskGulnara Seitova
Russian Children’s Clinical Hospital
Email: gulnara.seitova@medgenetics.ru
ORCID iD: 0000-0001-7525-0176
SPIN 代码: 7393-7228
MD, Cand. Sci. (Medicine)
俄罗斯联邦, Tomsk参考
- Semyachkina AN, Voskoboeva EYu, Voinova VYu, et al. The clinical and genetic aspects and pathogenic mechanisms of classical homocystinuria in children. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2013;58(3):30-37. EDN: QCKHMH
- Moiseev S, Chebotareva N, Bulanov N, et al. Classic homocystinuria: etiology, natural history and treatment. Klinicheskaya farmakologiya i terapiya = Clin Pharmacol Ther. 2022;31(3):30-37. doi: 10.32756/0869-54902022-3-30-37 EDN: HIZDWX
- Buchinskaya NV, Isupova EA, Kostik MM. Homocystinuria: literature review and clinical case description. Current Pediatrics. 2019;18(3):187-195. doi: 10.15690/vsp.v18i3.2036 EDN: NHOTMD
- Hoss GRW, Poloni S, Blom HJ, Schwartz IVD. Three main causes of homocystinuria: CBS, cblC and MTHFR deficiency. What do they have in common? JIEMS. 2019;7. doi: 10.1590/2326-4594-jiems-2019-0007
- Morris AAM, Kožich V, Santra S, et al. Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency. J. Inherited Metab. Dis. 2017;40(1):49-74. doi: 10.1007/s10545-016-9979-0
- Gan-Schreier H, Kebbewar M, Fang-Hoffmann J, et al. Newborn population screening for classic homocystinuria by determination of total homocysteine from guthrie cards. J. Pediatr. 2010;156(3):427–32. doi: 10.1016/j.jpeds.2009.09.054
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