Combined intake of glucose-and lipid-lowering medications further elevates plasma levels of PCSK9 in type 2 diabetes patients

被引:6
作者
Awadallah, Samir [1 ,2 ]
Taneera, Jalal [1 ,3 ]
Mohammed, Abdul Khader [1 ]
Unnikannan, Hema [1 ]
Sulaiman, Nabil [1 ,4 ]
机构
[1] Univ Sharjah, Sharjah Inst Med Res, Sharjah, U Arab Emirates
[2] Univ Sharjah, Coll Hlth Sci, Sharjah, U Arab Emirates
[3] Univ Sharjah, Dept Basic Med Sci, Coll Med, Sharjah, U Arab Emirates
[4] Univ Sharjah, Dept Family Med, Coll Med, Sharjah, U Arab Emirates
关键词
Diabetes mellitus; PCSK9; Statins; Insulin; Metformin; SUBTILISIN/KEXIN TYPE 9; CIRCULATING PCSK9; ASSOCIATION; CHOLESTEROL; INSULIN; LDL; ATORVASTATIN; FENOFIBRATE; EXPRESSION; CHILDREN;
D O I
10.1016/j.dsx.2020.10.028
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aim: This study examined the status of plasma levels of protein convertase subtilisin/kexin 9 (PCSK9) in association with glucose-and lipid-lowering medications in subjects with type 2 diabetes (T2D). Methods: This study comprised 177 diabetics and 115 non-diabetic subjects recruited from the United Arab Emirates National Diabetes Study (UAEDIAB). Clinical and biomedical data were collected by standard techniques. Plasma levels of PCSK9 were determined using ELISA. Results: PCSK9 levels were higher in diabetics than non-diabetics (P < 0.001). Diabetics with disease duration >5 years, HbA1c > 7.0%, or male subjects, had significantly higher levels of PCSK9 than their counterparts (P < 0.05). Regression analysis revealed that HbA1c and age are predictors for PCSK9 in T2D subjects. Diabetic subjects with abnormal lipids profile on lipid-lowering medications had a higher level of PCSK9 compared to those with normal lipids profile (85.6 +/- 40.5 vs. 63.7 +/- 39.5 ng/ml, respectively; P < 0.01). Diabetics on combined intake of insulin and oral glucose-lowering drugs had higher levels of PCSK9 than those not taking any (86.1 +/- 41.6 vs 69.7 +/- 36.1 ng/ml, respectively; P < 0.05). The highest levels of PCSK9 however, were in diabetics on combined lipid- and glucose-lowering therapy when compared to those, not on any (96.2 +/- 34.0 vs 66.0 +/- 35.1 ng/ml, respectively; P < 0.01). Conclusions: Age and HbA1c are the most predictors for the elevated levels of PCSK9 in Emirati T2D subjects. Combined therapy of glucose-and lipid-lowering medications further elevates plasma levels of PCSK9 in diabetic subjects. (C) 2020 Diabetes India. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2087 / 2092
页数:6
相关论文
共 44 条
[1]   Mutations in PCSK9 cause autosomal dominant hypercholesterolemia [J].
Abifadel, M ;
Varret, M ;
Rabès, JP ;
Allard, D ;
Ouguerram, K ;
Devillers, M ;
Cruaud, C ;
Benjannet, S ;
Wickham, L ;
Erlich, D ;
Derré, A ;
Villéger, L ;
Farnier, M ;
Beucler, I ;
Bruckert, E ;
Chambaz, J ;
Chanu, B ;
Lecerf, JM ;
Luc, G ;
Moulin, P ;
Weissenbach, J ;
Prat, A ;
Krempf, M ;
Junien, C ;
Seidah, NG ;
Boileau, C .
NATURE GENETICS, 2003, 34 (02) :154-156
[2]   The effect of insulin on circulating PCSK9 in postmenopausal obese women [J].
Awan, Zuhier ;
Dubuc, Genevieve ;
Faraj, May ;
Dufour, Robert ;
Seidah, Nabil G. ;
Davignon, Jean ;
Rabasa-Lhoret, Remi ;
Baass, Alexis .
CLINICAL BIOCHEMISTRY, 2014, 47 (12) :1033-1039
[3]   Plasma PCSK9 Is Associated with Age, Sex, and Multiple Metabolic Markers in a Population-Based Sample of Children and Adolescents [J].
Baass, Alexis ;
Dubuc, Genevieve ;
Tremblay, Michel ;
Delvin, Edgard E. ;
O'Loughlin, Jennifer ;
Levy, Emile ;
Davignon, Jean ;
Lambert, Marie .
CLINICAL CHEMISTRY, 2009, 55 (09) :1637-1645
[4]   Association between proprotein convertase subtilisin/kexin 9 (PCSK9) and lipoprotein subclasses in children with type 1 diabetes mellitus: Effects of glycemic control [J].
Bojanin, Dragana ;
Vekic, Jelena ;
Milenkovic, Tatjana ;
Vukovic, Rade ;
Zeljkovic, Aleksandra ;
Stefanovic, Aleksandra ;
Janac, Jelena ;
Ivanisevic, Jasmina ;
Mitrovic, Katarina ;
Miljkovic, Milica ;
Spasojevic-Kalimanovska, Vesna .
ATHEROSCLEROSIS, 2019, 280 :14-20
[5]   Plasma proprotein convertase subtilisin kexin type 9 is not altered in subjects with impaired glucose metabolism and type 2 diabetes mellitus, but its relationship with non-HDL cholesterol and apolipoprotein B may be modified by type 2 diabetes mellitus: The CODAM study [J].
Brouwers, M. C. G. J. ;
Troutt, J. S. ;
van Greevenbroek, M. M. J. ;
Ferreira, I. ;
Feskens, E. J. ;
van der Kallen, C. J. H. ;
Schaper, N. C. ;
Schalkwijk, C. G. ;
Konrad, R. J. ;
Stehouwer, C. D. A. .
ATHEROSCLEROSIS, 2011, 217 (01) :263-267
[6]   Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9 [J].
Careskey, Holly E. ;
Davis, R. Aleks ;
Alborn, William E. ;
Troutt, Jason S. ;
Cao, Guoqing ;
Konrad, Robert J. .
JOURNAL OF LIPID RESEARCH, 2008, 49 (02) :394-398
[7]   Association between plasma PCSK9 and gamma-glutamyl transferase levels in diabetic patients [J].
Cariou, Bertrand ;
Le Bras, Maelle ;
Langhi, Cedric ;
Le May, Cedric ;
Guyomarc'h-Delasalle, Beatrice ;
Krempf, Michel ;
Costet, Philippe .
ATHEROSCLEROSIS, 2010, 211 (02) :700-702
[8]   Plasma PCSK9 is increased by Fenofibrate and Atorvastatin in a non-additive fashion in diabetic patients [J].
Costet, P. ;
Hoffmann, M. M. ;
Cariou, B. ;
Delasalle, B. Guyomarc'h ;
Konrad, T. ;
Winkler, K. .
ATHEROSCLEROSIS, 2010, 212 (01) :246-251
[9]   Hepatic PCSK9 expression is regulated by nutritional status via insulin and sterol regulatory element-binding protein 1c [J].
Costet, P ;
Cariou, B ;
Lambert, G ;
Lalanne, F ;
Lardeux, B ;
Jarnoux, AL ;
Grefhorst, A ;
Stels, B ;
Krempf, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (10) :6211-6218
[10]   PCSK9 and its modulation [J].
Cui, Chuan-Jue ;
Li, Sha ;
Li, Jian-Jun .
CLINICA CHIMICA ACTA, 2015, 440 :79-86