From the Department of Pediatrics, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora (S.J.N., S.D.M.); Cardiology Section, Veterans Affairs Salt Lake City Health Care System and the Departments of Internal Medicine (Cardiology) and Pharmacology, University of Utah School of Medicine (M.M.); Division of Cardiology, Department of Medicine, University of Colorado Denver, Aurora (P.N., B.L.S., C.C.S.); and Division of Cardiology, Department of Medicine, Denver Health and Hospital Authority, CO (B.L.S.).
Circ Heart Fail. 2015 Jan;8(1):57-63. doi: 10.1161/CIRCHEARTFAILURE.114.001218. Epub 2014 Oct 2.
Despite the application of proven adult heart failure therapies to children with idiopathic dilated cardiomyopathy (IDC), prognosis remains poor. Clinical experience with phosphodiesterase 3 inhibitors (PDE3i) in pediatric patients with IDC, however, demonstrates improved heart failure symptoms without the increased incidence of sudden death seen in adults treated with PDE3i. We sought to determine age-related differences in PDE activity and associated intracellular signaling responsible for the efficacy and relative safety of chronic PDE3i in pediatric heart failure.
cAMP levels, PDE activity, and phospholamban phosphorylation (pPLB) were determined in explanted human left ventricular myocardium (pediatric n=41; adult n=88). Adults and children with IDC (not treated with PDE3i) had lower cAMP and pPLB compared with nonfailing controls. In contrast to their adult counterparts, pediatric IDC patients chronically treated with PDE3i had elevated cAMP (P=0.0403) and pPLB (P=0.0119). In addition, total PDE- and PDE3-specific activities were not altered in pediatric IDC patients on PDE3i, whereas adult IDC patients on PDE3i demonstrated higher total PDE-specific (74.6±13.8 pmol/mg per minute) and PDE3-specific (48.2±15.9 pmol/mg per minute) activities in comparison with those of nonfailing controls (59.5±14.4 and 35.5±12.8 pmol/mg per minute, respectively).
Elevated cAMP and higher pPLB may contribute to sustained hemodynamic benefits in pediatric IDC patients treated with PDE3i. In contrast, higher total PDE and PDE3 activities in adult IDC patients treated with PDE3i may perpetuate lower myocardial cAMP and pPLB levels, limiting the potential benefits of PDE3i therapy.
尽管已将成熟的成人心力衰竭治疗方法应用于特发性扩张型心肌病(IDC)患儿,但预后仍然不佳。然而,在患有 IDC 的儿科患者中应用磷酸二酯酶 3 抑制剂(PDE3i)的临床经验表明,心力衰竭症状得到改善,而接受 PDE3i 治疗的成年人中未见增加的猝死发生率。我们试图确定 PDE 活性和相关细胞内信号转导在小儿心力衰竭中慢性 PDE3i 疗效和相对安全性中的年龄相关差异。
在离体人心肌组织(儿科 n=41;成人 n=88)中测定 cAMP 水平、PDE 活性和磷蛋白磷酸化(pPLB)。与非衰竭对照组相比,IDC 患儿和成人 IDC 患者的 cAMP 和 pPLB 水平较低。与成人 IDC 患者相比,接受 PDE3i 慢性治疗的小儿 IDC 患者的 cAMP(P=0.0403)和 pPLB(P=0.0119)升高。此外,在接受 PDE3i 治疗的小儿 IDC 患者中,总 PDE-和 PDE3 特异性活性并未改变,而接受 PDE3i 治疗的成人 IDC 患者的总 PDE 特异性(74.6±13.8 pmol/mg·min)和 PDE3 特异性(48.2±15.9 pmol/mg·min)活性均高于非衰竭对照组(分别为 59.5±14.4 和 35.5±12.8 pmol/mg·min)。
在接受 PDE3i 治疗的小儿 IDC 患者中,cAMP 升高和 pPLB 升高可能有助于维持血液动力学获益。相反,接受 PDE3i 治疗的成人 IDC 患者中总 PDE 和 PDE3 活性更高可能会导致心肌 cAMP 和 pPLB 水平降低,限制 PDE3i 治疗的潜在获益。