Lipids in Health and Disease | |
Nutraceutical pill containing berberine versus ezetimibe on plasma lipid pattern in hypercholesterolemic subjects and its additive effect in patients with familial hypercholesterolemia on stable cholesterol-lowering treatment | |
Stefano Bertolini1  Antonella Bellocchio1  Livia Pisciotta1  | |
[1] Department of Internal Medicine, University of Genoa, Viale Benedetto XV n. 6, 16132, Genoa, Italy | |
关键词: PCSK9; Familial Hypercholesterolemia; Primary polygenic hypercholesterolemia; Ezetimibe; Berberine; | |
Others : 1160195 DOI : 10.1186/1476-511X-11-123 |
|
received in 2012-04-27, accepted in 2012-09-21, 发布年份 2012 | |
【 摘 要 】
Background
Although statins (STs) are drugs of first choice in hypercholesterolemic patients, especially in those at high cardiovascular risk, some of them are intolerant to STs or refuse treatment with these drugs. In view of this, we have evaluated the lipid-lowering effect of a nutraceutical pill containing berberine (BBR) and of ezetimibe, as alternative treatments, in monotherapy or in combination, in 228 subjects with primary hypercholesterolemia (HCH), with history of STs intolerance or refusing STs treatment. In addition, since PCSK9 was found up-regulated by STs dampening their effect through an LDL receptors (LDLRs) degradation, and BBR suppressed PCSK9 expression in cellular studies, we supplemented the stable lipid-lowering therapy of 30 genotype-confirmed Familial Hypercholesterolemia heterozygotes (HeFH) with BBR, searching for a further plasma cholesterol reduction. Plasma lipid pattern was evaluated at baseline and during treatments.
Results
In HCH subjects the nutraceutical pill resulted more effective than EZE in lowering LDL cholesterol (−31.7% vs −25.4%, P < 0.001) and better tolerated. On treatment, LDL-C level below 3.36 mmol/L (≤130 mg/dl) was observed in 28.9% of subjects treated with the nutraceutical pill and 11.8% of those treated with EZE (P <0.007). In the group treated with EZE the subjects carrying the G allele of the g.1679 C > G silent polymorphism of NPC1L1 gene showed a higher response to EZE than homozygous for the common allele (GG + CG: LDL-C −29.4±5.0%, CC −23.6±6.5%, P <0.001). Combined treatment with these drugs was as effective as STs in moderate doses (LDL cholesterol −37%, triglycerides −23%). In HeFH patients the addition of BBR resulted in LDL cholesterol reductions inversely related to those induced by the stable therapy (r = −0.617, P <0.0001), with mean 10.5% further decrease.
Conclusions
The alternative treatments tested in our HCH subjects were rather effective and safe. The findings in HeFH patients suggest that BBR might act in vivo increasing expression and stability of LDLRs and/or suppressing PCSK9 expression.
【 授权许可】
2012 Pisciotta et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20150410095558643.pdf | 321KB | download | |
Figure 5. | 78KB | Image | download |
Figure 1 . | 35KB | Image | download |
【 图 表 】
Figure 1 .
Figure 5.
【 参考文献 】
- [1]Cleeman JI: Executive summary of the third report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). JAMA 2001, 285:2486-2497.
- [2]Catapano AL, Reiner Z, De Backer G, Grahan I, Taskinen M-R, Wiklund O, Agewall S, Alegria E, Chapman MJ, Durrington P, Erdine S, Halcox J, Hobbs R, Kjekshus J, Perrone Filardi P, Riccardi G, Storey R, Wood D: ESC/EAS guidelines for the management of dyslipidaemias. The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). Atherosclerosis 2011, 217S:S1-S44.
- [3]Lewis SJ: Lipid-lowering therapy: who can benefit? Vasc Health Risk Manag 2011, 7:525-534.
- [4]Cholesterol Treatment Trialists’ (CTT) Collaboration: Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomized trial. Lancet 2010, 376:1670-1681.
- [5]Mills EJ, O’Regan C, Eyawo O, Wu P, Mills F, Berwanger O, Briel M: Intensive statin therapy compared with moderate dosing for prevention of cardiovascular events: a meta-analysis of >40 000 patients. Eur Heart J 2011, 32:1409-1415.
- [6]Abd TT, Jacobson TA: Statin-induced myopathy : a review and update. Expert Opin Drug Saf 2011, 10:373-387.
- [7]Arca M, Pigna G: Treating statin-intolerant patients. Diabetes Metab Syndr Obes 2011, 4:155-166.
- [8]Costet P: Molecular pathways and agents for lowering LDL-cholesterol in addition to statins. Pharmacol Ther 2010, 126:263-278.
- [9]Adouridis A, Filippatos TD, Tsimihodimos V, Elisaf MS: Combinations of ezetimibe with nonstatin drug regimens affecting lipid metabolism. Expert Rev Cardiovasc Ther 2011, 9:355-366.
- [10]Cariou B, Le May C, Costet P: Clinical aspects of PCSK9. Atherosclerosis 2011, 216:258-265.
- [11]Cameron J, Ranheim T, Kulseth MA, Leren TP, Berge KE: Berberine decrease PCSK9 expression in HepG2 cells. Atherosclerosis 2008, 201:266-273.
- [12]Bertolini S, Cantafora A, Averna M, Cortese C, Motti C, Martini S, Pes G, Postiglione A, Stefanutti C, Blotta I, Pisciotta L, Rolleri M, Langheim S, Ghibellini M, Rabbone I, Calandra S: Clinical expression of Familial Hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype. Arterioscler Thromb Vasc Biol 2000, 20:e41-e52.
- [13]Simon JS, Karnoub MC, Devlin DJ, Arreaza MG, Qiu P, Monks SA, Severino ME, Deutsch P, Palmisano J, Sachs AB, Bayne ML, Plump AS, Schadt EE: Sequence variation in NPC1L1 and association with improved LDL-cholesterol lowering in response to ezetimibe treatment. Genomics 2005, 86:648-656.
- [14]Pisciotta L, Fasano T, Bellocchio A, Bocchi L, Sallo R, Fresa R, Col angeli I, Cantafora A, Calandra S, Bertolini S: Effect of ezetimibe coadministered with statins in genotype-confirmed heterozygous FH patients. Atherosclerosis 2007, 194:e116-e122.
- [15]Cicero AFG, Rovati L, Setnikar I: Eulipidemic effects of berberine administered alone or in combination with other natural cholesterol-lowering agents in humans. Arzneimittelforschung 2007, 57:26-30.
- [16]Affuso F, Ruvolo A, Micillo F, Saccà L, Fazio S: Effects of a nutraceutical combination (berberine, red yeast rice and policosanols) on lipid levels and endothelial function randomized, double-blind, placebo-controlled study. Nutr Metab Cardiovasc Dis 2010, 20:656-661.
- [17]Marazzi G, Cacciotti L, Pelliccia F, Iaia L, Volterrani M, Caminiti G, Sposato B, Massaro R, Greco F, Rosano G: Long-term effects of Nutraceuticals (Berberine, red yeast rice, policosanol) in elderly hypercholesterolemic patients. Adv Ther 2011, 28:1105-1113.
- [18]Trimarco B, Benvenuti C, Rozza F, Cimmino CS, Giudice R, Crispo S: Clinical evidence of efficacy of red yeast rice and berberine in a large controlled study versus diet. Mediterr J Nutr Metab 2011, 4:133-139.
- [19]Huang J, Frohlich J, Ignaszewski AP: The impact of dietary changes and dietary supplements on lipid profile. Can J Cardiol 2011, 27:488-505.
- [20]Halbert SC, French B, Gordon RY, Farrar JT, Schmitz K, Morris PB, Thompson PD, Rader DJ, Becker DJ: Tolerability of red yeast rice (2,400 mg twice daily) versus pravastatin (20 mg twice daily) in patients with previous statin intolerance. Am J Cardiol 2010, 105:198-204.
- [21]Venero CV, Venero JV, Wortham DC, Thompson PD: Lipid-lowering efficacy of red yeast rice in a population intolerant to statins. Am J Cardiol 2010, 105:664-666.
- [22]Gordon RY, Cooperman T, Obermeyer W, Becker DJ: Marked variability of monacolin levels in commercial red yeast rice products. Arch Intern Med 2010, 170:1722-1727.
- [23]Berthold HK, Unverdorben S, Degenhardt R, Bulitta M, Gouni-Berthold I: Effect of policosanol on lipid levels among patients with hypercholesterolemia or combined hyperlipidemia. JAMA 2006, 295:2262-2269.
- [24]Backes JM, Gibson CA, Ruisinger JF, Moriarty PM: Modified-policosanol does not reduce plasma lipoproteins in hyperlipidemic patients when used alone or in combination with statin therapy. Lipids 2011, 46:923-929.
- [25]Kong W, Wei J, Abidi P, Lin M, Inaba S, Li C, Wang Y, Wang Z, Si S, Pan H, Wang S, Wu J, Wang Y, Li Z, Liu J, Jiang J-D: Berberine is a novel cholesterol-lowering drug working through a unique mechanism distinct from statins. Nat Med 2004, 10:1344-1351.
- [26]Li H, Chen W, Zhou Y, Abidi P, Sharpe O, Robinson WH, Kraemer FB, Liu J: Identification of mRNA binding proteins that regulate the stability of LDL receptor mRNA through AU-rich elements. J Lipid Res 2009, 50:820-831.
- [27]Lee S, Lim HJ, Park JH, Lee KS, Jang Y, Park HY: Berberine induced LDLR up-regulation involves JNK pathway. Biochem Biophys Res Commun 2007, 362:853-857.
- [28]Brusq JM, Ancellin N, Grondin P, Guillard R, Martin S, Saintillan Y, Issandou M: Inhibition of lipid synthesis through activation of AMP kinase: an additional mechanism for the hypolipidemic effects of berberine. J Lipid Res 2006, 47:1281-1288.
- [29]Phan BAP, Dayspring TD, Toth PP: Ezetimibe therapy: mechanism of action and clinical update. Vasc Health Risk Manag 2012, 8:415-427.
- [30]Tremblay AJ, Lamarche B, Cohn JS, Hogue JC, Couture P: Effect of ezetimibe on the in vivo kinetics of apoB-48 and apoB-100 in men with primary hypercholesterolemia. Arterioscler Thromb Vasc Biol 2006, 26:1101-1106.
- [31]Descamps OS, De Sutter J, Guillaume M, Missault L: Where does the interplay between cholesterol absorption and synthesis in the context of statin and/or ezetimibe treatment stand today? Atherosclerosis 2011, 217:308-321.
- [32]Mikhailidis DP, Lawson RW, McCormick AL, Sibbring GC, Tershakovec AM, Davies GM, Tunceli K: Comparative efficacy of the addition of ezetimibe to statin vs statin titration in patients with hypercholesterolemia: systematic review and meta-analysis. Curr Med Res Opin 2011, 27:1191-1210.
- [33]Pandor A, Ara RM, Tumur I, Wilkinson AJ, Paisley S, Duenas A, Durrington PN, Chilcott J: Ezetimibe monotherapy for cholesterol lowering in 2,722 people: systematic review and meta-analysis of randomized controlled trials. J Intern Med 2009, 265:568-580.
- [34]Derdemezis CS, Filippatos TD, Tselepis AD, Mikhailidis DP, Elisaf MS: Effect of ezetimibe, either alone or in combination with atorvastatin, on serum vistatin levels: a pilot study. Expert Opin Pharmacother 2008, 9:1829-1837.
- [35]Weng TC, Yang YHK, Lin S-J, Tai SH: A systematic review and meta-analysis on the therapeutic equivalence of statins. J Clin Pharm Ther 2010, 35:139-151.
- [36]Horton JD, Cohen JC, Hobbs HH: PCSK9: a convertase that coordinates LDL catabolism. J Lipid Res 2009, 50:S172-S177.
- [37]Li H, Dong B, Park SW, Lee HS, Chen W, Liu J: Hepatocyte nuclear factor 1α plays a critical role in PCSK9 gene transcription and regulation by the natural hypocholesterolemic compound berberina. J Biol Chem 2009, 42:28885-28895.
- [38]Dubuc G, Chamberland A, Wassef H, Davignon J, Seidah NG, Bernier L, Prat A: Statins upregulate PCSK9, the gene encoding the proprotein convertase neural apoptosis-regulated convertase-1 implicated in Familial Hypercholesterolemia. Arterioscler Thromb Vasc Biol 2004, 24:1454-1459.
- [39]Dubuc G, Tremblay M, Paré G, Jacques H, Hamelin J, Benjannet S, Boulet L, Genest J, Bernier L, Seidah NG, Davignon J: A new method for measurement of total plasma PCSK9: clinical applications. J Lipid Res 2010, 51:140-149.
- [40]Konrad RJ, Troutt JS, Cao G: Effects of currently prescribed LDL-C lowering drugs on PCSK9 and implications for the next generation of LDL-C lowering agents. Lipids Health Dis 2011, 10:38. BioMed Central Full Text
- [41]Rashid S, Curtis DE, Garuti R, Anderson NN, Bashmakov Y, Ho YK, Hammer RE, Moon YA, Horton JD: Decreased plasma cholesterol and hypersensitivity to statins in mice lacking PCSK9. Proc Natl Acad Sci USA 2005, 102:5374-5379.
- [42]Berge KE, Ose L, Leren TP: Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy. Arterioscler Thromb Vasc Biol 2006, 26:1094-1100.
- [43]Tibolla G, Norata GD, Artali R, Meneghetti F, Catalano AL: Proprotein convertase subtilisin/kexin type 9 (PCSK9): from structure-function relation to therapeutic inhibition. Nutr Metab Cardiovasc Dis 2011, 21:835-843.
- [44]Dong B, Wu M, Li H, Kraemer FB, Adeli K, Seidah NG, Park SW, Liu J: Strong induction of PCSK9 gene expression through HNF1α and SREBP2: mechanism for the resistance to LDL-cholesterol lowering effect of statins in dyslipidemic hamster. J Lipid Res 2010, 51:1486-1495.
- [45]Kong WJ, Wei J, Zuo ZY, Wang YM, Song DQ, You XF, Zhao LX, Pan HN, Jiang JD: Combination of simvastatin with berberine improves the lipid-lowering effect. Metabolism 2008, 57:1029-1037.
- [46]Awan Z, Seidah NG, MacFadyen JG, Benjannet S, Chasman DI, Ridker PM, Genest J: Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER Trial. Clin Chem 2012, 58:183-189.