医学
肾病
血管紧张素II
药理学
敌手
内皮素受体
血管紧张素II受体拮抗剂
内皮素受体拮抗剂
血管紧张素受体
血管紧张素Ⅱ受体1型
受体拮抗剂
内科学
内分泌学
受体
糖尿病
作者
Gates B. Colbert,Hector Madariaga,Anna Gaddy,Mohamed E. Elrggal,Edgar V. Lerma
标识
DOI:10.1080/17512433.2025.2532659
摘要
IgA nephropathy (IgAN) is the most common primary glomerulonephritis. For decades, the only medication treatments that were widely accepted were the use of renin-angiotensin aldosterone inhibitors and corticosteroids. The early 2020s have brought a flurry of new treatments to the once dark IgA treatment landscape. Sparsentan is a novel dual-endothelin angiotensin receptor antagonist that has been approved as an add-on therapy for the treatment of IgAN. We discuss the treatment landscape and the unmet needs for treating IgA nephropathy. Multiple clinical trials showing the efficacy of sparsentan including DUET, PROTECT, SPARTACUS, and SPARTAN will be described. Additionally, we will preview the future options for IgA patients. Sparsentan is a major step forward in improving outcomes for patients with IgAN. This once-a-day agent, in addition to other standards of care, limits proteinuria and progression to ESKD and kidney transplantation. The ability to lower proteinuria without weakening the immune system is a substantial gain for patients. As an agent that impacts the glomeruli directly, sparsentan is able to limit damage in mechanisms that previous RASi and steroids have not. Including sparsentan in the combination treatment for IgAN must be considered for adequate kidney protection.
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