Wang Wei, Tran Pamela V
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas, USA; The Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas, USA.
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas, USA; The Jared Grantham Kidney Institute, University of Kansas Medical Center, Kansas City, Kansas, USA.
Kidney Int. 2022 May;101(5):870-872. doi: 10.1016/j.kint.2022.02.008.
Pharmacotherapies that are safe during pregnancy are lacking for patients with autosomal dominant polycystic kidney disease. In this issue, Daneshgar et al. reveal that administration of the mitochondrial-protective peptide, elamipretide, during pregnancy and lactation in a mouse model with autosomal dominant polycystic kidney disease, is nonteratogenic and attenuates disease severity in both mothers and their affected offspring. This finding suggests therapeutic potential of elamipretide during pregnancy, in utero, and in early postnatal life.
对于患有常染色体显性多囊肾病的患者而言,孕期安全的药物治疗方法尚不存在。在本期杂志中,达内什加尔等人揭示,在患有常染色体显性多囊肾病的小鼠模型中,孕期和哺乳期给予线粒体保护肽艾拉米肽,不会产生致畸作用,并且会减轻母亲及其患病后代的疾病严重程度。这一发现表明艾拉米肽在孕期、子宫内及出生后早期具有治疗潜力。