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Xuezhikang Therapy Increases miR-33 Expression in Patients with Low HDL-C Levels
Author(s) -
Ruihua Cao,
Yongyi Bai,
Lan Sun,
Jin Zheng,
Mian Zu,
Guanhua Du,
Ping Ye
Publication year - 2014
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2014/781780
Subject(s) - expression (computer science) , microrna , medicine , biology , oncology , genetics , computer science , gene , programming language
Background . MicroRNA-33a and -b (miR-33a/b) have been revealed to be posttranscriptional regulators of HDL metabolism. Xuezhikang (XZK) is a marked natural HDL-raising polypill. We aim to evaluate the effects of XZK on the expression of circulating miR-33a/b in patients with low plasma HDL-C levels. Methods . A total of 42 participating patients with low baseline levels of HDL cholesterol were assigned to receive an XZK capsule, 600 mg twice daily for 6 months. The expression of circulating miR-33a/b was detected at baseline and after XZK therapy measured with quantitative reverse-transcription (RT) polymerase chain reaction (PCR). Results . The mean (SD) HDL-C level after XZK treatment was 1.19 (0.13) mmol/L, representing an increase of 11.2% from baseline ( P < 0.001). Q-PCR analysis of plasma miRNAs revealed an increase in relative miR-33a/b expression with XZK treatment. The miR-33a expression was raised from 0.81 to 1.73 ( P = 0.012); miR-33b expression was increased from 1.2 to 2.75 ( P < 0.001). The changes of miR-33a and miR-33b were inversely related to the posttreatment LDL-C levels ( r = −0.37, P = 0.019; r = −0.33, P = 0.035, resp.). Conclusion . In patients with low HDL-C levels, XZK therapy raised plasma levels of miR-33a and miR-33b, which may inhibit cellular cholesterol export and limit the HDL-raising effect of XZK.

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