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Orphanet journal of rare diseases · 2013

Weekly oral alendronate in mevalonate kinase deficiency.

Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Cantarini Luca, Vitale Antonio, Magnotti Flora, Lucherini Orso Maria, Caso Francesco, Frediani Bruno, Galeazzi Mauro, Rigante Donato

Аннотация

BACKGROUND: Mevalonate kinase deficiency (MKD) is caused by mutations in the MVK gene, encoding the second enzyme of mevalonate pathway, which results in subsequent shortage of downstream compounds, and starts in childhood with febrile attacks, skin, joint, and gastrointestinal symptoms, sometimes induced by vaccinations.

METHODS: For a history of early-onset corticosteroid-induced reduction of bone mineral density in a 14-year-old boy with MKD, who also had presented three bone fractures, we administered weekly oral alendronate, a drug widely used in the management of osteoporosis and other high bone turnover diseases, which blocks mevalonate and halts the prenylation process.

RESULTS: All of the patient's MKD clinical and laboratory abnormalities were resolved after starting alendronate treatment.

CONCLUSIONS: This observation appears enigmatic, since alendronate should reinforce the metabolic block characterizing MKD, but is crucial because of the ultimate improvement shown by this patient. The anti-inflammatory properties of bisphosphonates are a new question for debate among physicians across various specialties, and requires further biochemical and clinical investigation.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты