New perspectives on CKD-induced dyslipidemia

被引:37
作者
Bermudez-Lopez, Marcelino [1 ]
Arroyo, David [1 ]
Betriu, Angels [1 ]
Masana, Luis [2 ]
Fernandez, Elvira [1 ]
Valdivielso, Jose M. [1 ]
机构
[1] REDinREN ISCIII, Vasc & Renal Translat Res Grp, Inst Biomed Res Lleida IRBLleida, Lleida, Spain
[2] Univ Rovira & Virgili, Unitat Med Vasc & Metab, St Joan Univ Hosp, IISPV,CIBERDEM, Reus, Spain
关键词
Atherosclerosis; cardiovascular disease; chronic kidney disease; dyslipidemia; lipoproteins; CHRONIC KIDNEY-DISEASE; CHRONIC-RENAL-FAILURE; TYPE-2; DIABETES-MELLITUS; HIGH-DENSITY-LIPOPROTEIN; CARDIOVASCULAR-DISEASE; RISK-FACTORS; SUBCLINICAL ATHEROMATOSIS; HEMODIALYSIS-PATIENTS; LIPID ABNORMALITIES; PERITONEAL-DIALYSIS;
D O I
10.1080/14728222.2017.1369961
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Chronic kidney disease (CKD) is a world-wide health concern associated with a significantly higher cardiovascular morbidity and mortality. One of the principal cardiovascular risk factors is the lipid profile. CKD patients have a more frequent and progressive atheromatous disease that cannot be explained by the classical lipid parameters used in the daily clinical practice. Areas covered: The current review summarizes prevailing knowledge on the role of lipids in atheromathosis in CKD patients, including an overview of lipoprotein metabolism highlighting the CKD-induced alterations. Moreover, to obtain information beyond traditional lipid parameters, new state-of-the-art technologies such as lipoprotein subfraction profiling and lipidomics are also reviewed. Finally, we analyse the potential of new lipoprotein subclasses as therapeutic targets in CKD. Expert opinion: The CKD-induced lipid profile has specific features distinct from the general population. Besides quantitative alterations, renal patients have a plethora of qualitative lipid alterations that cannot be detected by routine determinations and are responsible for the excess of cardiovascular risk. New parameters, such as lipoprotein particle number and size, together with new biomarkers obtained by lipidomics will personalize the management of these patients. Therefore, nephrologists need to be aware of new insights into lipoprotein metabolism to improve cardiovascular risk assessment.
引用
收藏
页码:967 / 976
页数:10
相关论文
共 82 条
[1]   Lipidomic Signature of Progression of Chronic Kidney Disease in the Chronic Renal Insufficiency Cohort [J].
Afshinnia, Farsad ;
Rajendiran, Thekkelnaycke M. ;
Karnovsky, Alla ;
Soni, Tanu ;
Wang, Xue ;
Xie, Dawei ;
Yang, Wei ;
Shafi, Tariq ;
Weir, Matthew R. ;
He, Jiang ;
Brecklin, Carolyn S. ;
Rhee, Eugene P. ;
Schelling, Jeffrey R. ;
Ojo, Akinlolu ;
Feldman, Harold ;
Michailidis, George ;
Pennathur, Subramaniam .
KIDNEY INTERNATIONAL REPORTS, 2016, 1 (04) :256-268
[2]   Circulating angiotensin converting enzyme 2 activity as a biomarker of silent atherosclerosis in patients with chronic kidney disease [J].
Anguiano, Lidia ;
Riera, Marta ;
Pascual, Julio ;
Valdivielso, Jose Manuel ;
Barrios, Clara ;
Betriu, Angels ;
Clotet, Sergi ;
Mojal, Sergi ;
Fernandez, Elvira ;
Soler, Maria Jose .
ATHEROSCLEROSIS, 2016, 253 :135-143
[3]   Observational multicenter study to evaluate the prevalence and prognosis of subclinical atheromatosis in a Spanish chronic kidney disease cohort: baseline data from the NEFRONA study [J].
Arroyo, David ;
Betriu, Angels ;
Martinez-Alonso, Montserrat ;
Vidal, Teresa ;
Manuel Valdivielso, Jose ;
Fernandez, Elvira .
BMC NEPHROLOGY, 2014, 15
[4]   Value of high-density lipoprotein (HDL) subpopulations in predicting recurrent cardiovascular events in the Veterans Affairs HDL Intervention Trial [J].
Asztalos, BF ;
Collins, D ;
Cupples, LA ;
Demissie, S ;
Horvath, KV ;
Bloomfield, HE ;
Robins, SJ ;
Schaefer, EJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2185-2191
[5]   The effects of lowering LDL cholesterol with simvastatin plus ezetimibe in patients with chronic kidney disease (Study of Heart and Renal Protection): a randomised placebo-controlled trial [J].
Baigent, Colin ;
Landray, Martin J. ;
Reith, Christina ;
Emberson, Jonathan ;
Wheeler, David C. ;
Tomson, Charles ;
Wanner, Christoph ;
Krane, Vera ;
Cass, Alan ;
Craig, Jonathan ;
Neal, Bruce ;
Jiang, Lixin ;
Hooi, Lai Seong ;
Levin, Adeera ;
Agodoa, Lawrence ;
Gaziano, Mike ;
Kasiske, Bertram ;
Walker, Robert ;
Massy, Ziad A. ;
Feldt-Rasmussen, Bo ;
Krairittichai, Udom ;
Ophascharoensuk, Vuddidhej ;
Fellstrom, Bengt ;
Holdaas, Hallvard ;
Tesar, Vladimir ;
Wiecek, Andrzej ;
Grobbee, Diederick ;
de Zeeuw, Dick ;
Gronhagen-Riska, Carola ;
Dasgupta, Tanaji ;
Lewis, David ;
Herrington, William ;
Mafham, Marion ;
Majoni, William ;
Wallendszus, Karl ;
Grimm, Richard ;
Pedersen, Terje ;
Tobert, Jonathan ;
Armitage, Jane ;
Baxter, Alex ;
Bray, Christopher ;
Chen, Yiping ;
Chen, Zhengming ;
Hill, Michael ;
Knott, Carol ;
Parish, Sarah ;
Simpson, David ;
Sleight, Peter ;
Young, Alan ;
Collins, Rory .
LANCET, 2011, 377 (9784) :2181-2192
[6]   Risk factors for atherosclerosis in patients with chronic kidney disease: recognition and management [J].
Balla, Sudarshan ;
Nusair, Maen B. ;
Alpert, Martin A. .
CURRENT OPINION IN PHARMACOLOGY, 2013, 13 (02) :192-199
[7]   Diabetic nephropathy is an independent factor associated to severe subclinical atheromatous disease [J].
Barrios, Clara ;
Pascual, Julio ;
Otero, Sol ;
Soler, Maria J. ;
Rodriguez, Eva ;
Collado, Silvia ;
Faura, Anna ;
Mojal, Sergi ;
Navarro-Gonzalez, Juan F. ;
Betriu, Angels ;
Fernandez, Elvira ;
Valdivielso, Jose M. .
ATHEROSCLEROSIS, 2015, 242 (01) :37-44
[8]   Statistical methods for the analysis of high-throughput metabolomics data [J].
Bartel, Joerg ;
Krumsiek, Jan ;
Theis, Fabian J. .
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2013, 4 (05)
[9]   Lipoprotein metabolism and CKD: overview [J].
Barter, Philip .
CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2014, 18 (02) :243-246
[10]   Statins decrease all-cause mortality only in CKD patients not requiring dialysis therapy-A meta-analysis of 11 randomized controlled trials involving 21,295 participants [J].
Barylski, Marcin ;
Nikfar, Shekoufeh ;
Mikhailidis, Dimitri P. ;
Toth, Peter P. ;
Salari, Pooneh ;
Ray, Kausik K. ;
Pencina, Michael J. ;
Rizzo, Manfredi ;
Rysz, Jacek ;
Abdollahi, Mohammad ;
Nicholls, Stephen J. ;
Banach, Maciej .
PHARMACOLOGICAL RESEARCH, 2013, 72 :35-44