Orphanet Journal of Rare Diseases· 2026Q1
Metilmalonik asidemi ve ileri evre kronik böbrek hastalığı olan yetişkin kardeşlerde uzun süreli karglumik asit tedavisi
Long-term carglumic acid therapy in adult siblings with methylmalonic acidemia and advanced chronic kidney disease
- 0atıf
- Q1SCImago
- 2026yıl
Kısa özet
Metilmalonik asidemi (MMA) ve ileri evre kronik böbrek hastalığı (KBH) olan iki yetişkin kardeş, 40 aya kadar süren uzun süreli karglumik asit (CA) tedavisi ile metabolik dekompansasyonlar ve hastaneye yatışlar açısından stabilize edildi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- MMA ve ileri evre KBH'si olan iki yetişkin kardeş, 40 aya kadar uzun süreli karglumik asit (CA) ile tedavi edildi.
- CA tedavisi, stabil plazma amonyak seviyelerine ve daha az metabolik dekompansasyon ile hastaneye yatışlara yol açtı.
- Hastalar, CA tedavisi sırasında diyet toleransı ve günlük işlevsellikte iyileşmeler gösterdi.
- Her iki hastada da CA ile ilişkili herhangi bir yan etki gözlenmedi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
Abstract Background Evidence supporting long-term carglumic acid (CA) therapy in adult patients with methylmalonic acidemia (MMA), particularly those with advanced chronic kidney disease (CKD) or dialysis dependence, is extremely limited. Adult patients with MMA frequently experience recurrent metabolic decompensation and progressive multi-organ complications, for which effective chronic stabilization strategies are lacking. We describe the long-term clinical course of two adult siblings with MMA caused by pathogenic MMUT variants who were unresponsive to vitamin B12 therapy and developed advanced CKD. Both patients experienced frequent metabolic decompensation despite standard management. CA was initiated as adjunctive long-term therapy and patients were followed for up to 40 months. Results Following CA initiation, both siblings maintained stable plasma ammonia levels and had fewer metabolic decompensation episodes and hospitalizations. Improved dietary tolerance and daily functioning were also observed during follow-up. Longitudinal urinary methylmalonic acid levels fluctuated during treatment. No adverse events considered related to CA were observed in either patient during the treatment period. Conclusions These cases describe sustained clinical stability during long-term CA treatment in two adult siblings with MMA and advanced CKD, including dialysis dependence. CA may have a role as an adjunctive therapy during prolonged waiting periods prior to liver–kidney transplantation. Because of the case-based design and concomitant supportive treatments, further studies are needed to evaluate the potential role of long-term CA in this population.
Yazarların özeti; kaynağından alınmıştır. Orphanet Journal of Rare Diseases, 2026 · DOI ↗
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Alan: Klinik Biyokimya
Clinical BiochemistryBiochemistry, Genetics and Molecular Biology