Simha Vinaya, Qin Sisi, Shah Pankaj, Smith Byron H, Kremers Walter K, Kushwaha Sudhir, Wang Liewei, Pereira Naveen L
Division of Endocrinology, Mayo Clinic, Rochester, MN, USA.
Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, 200 First Street SW, Rochester, MN, 55905, USA.
J Cardiovasc Transl Res. 2017 Feb;10(1):9-15. doi: 10.1007/s12265-016-9719-8. Epub 2016 Dec 27.
Sirolimus used in transplantation is often associated with hypercholesterolemia. We measured serum lipid and PCSK9 levels in 51 heart transplant recipients who had their immunosuppressive therapy switched from calcineurin inhibitors to sirolimus. The switch resulted in a 23% increase in LDL cholesterol, and 46% increase in triglycerides and PCSK9 levels increased from 316 ± 105 ng/mL to 343 ± 107 ng/mL (p = 0.04), however the change in PCSK9 levels did not correlate with an increase in lipid levels (p = 0.2). To investigate the mechanism for the variability in the change in PCSK9 levels, lymphoblastoid cell lines were incubated with both sirolimus and everolimus, resulting in a 2-3 fold increase in PCSK9 expression and protein levels in mTOR inhibitor sensitive but not in mTOR inhibitor resistant cell lines. This first in human study demonstrates that sirolimus therapy is associated with elevation in PCSK9 levels which is not associated with sirolimus-induced hypercholesterolemia.
用于移植的西罗莫司常与高胆固醇血症相关。我们测量了51名心脏移植受者的血脂和前蛋白转化酶枯草溶菌素9(PCSK9)水平,这些受者将免疫抑制治疗从钙调神经磷酸酶抑制剂转换为西罗莫司。这种转换导致低密度脂蛋白胆固醇增加23%,甘油三酯增加46%,PCSK9水平从316±105 ng/mL增至343±107 ng/mL(p = 0.04),然而PCSK9水平的变化与血脂水平的升高并无相关性(p = 0.2)。为研究PCSK9水平变化的机制,将淋巴母细胞系与西罗莫司和依维莫司共同孵育,结果显示在对雷帕霉素靶蛋白(mTOR)抑制剂敏感的细胞系中PCSK9表达和蛋白水平增加了2至3倍,而在对mTOR抑制剂耐药的细胞系中未出现这种情况。这项首次在人体进行的研究表明,西罗莫司治疗与PCSK9水平升高相关,而这与西罗莫司诱导的高胆固醇血症无关。