Update on the role of the atherogenic lipoprotein phenotype in cardiovascular prevention

被引:1
作者
Rizzo, Manfredi [1 ]
Berneis, Kaspar [2 ]
机构
[1] Univ Palermo, Dipartimento Med Clin & Patol Emergenti, Via Vespro 141, I-90127 Palermo, Italy
[2] Univ Hosp Zurich, Clin Endocrinol Diabet & Clin Nutr, Zurich, Switzerland
关键词
atherogenic lipoprotein phenotype; dense LDL; gradient gel electrophoresis; HDL-cholesterol; triglycerides;
D O I
10.2217/14796678.3.5.553
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Higher plasma triglyceride levels and decreased HDL-cholesterol concentrations are usually accompanied by the presence of small, dense LDL in the so-called lipid triad or 'atherogenic lipoprotein phenotype'. This phenotype is highly atherogenic and its prevalence may suggest an even higher overall burden of atherosclerotic disease as compared with that associated with hypercholesterolemia. As stated by the National Cholesterol Education Program Adult Treatment Panel III, there is evidence suggesting each component of this lipid triad is individually atherogenic. However, the relative contribution of each component cannot be easily determined. Therefore, it has been suggested to consider the atherogenic lipoprotein phenotype as a whole as a risk factor. This is supported by data from epidemiological studies considering high-risk populations, which showed that the contribution to cardiovascular risk of each individual component cannot be dissected from the sum of all factors. We recently investigated the prevalence of the atherogenic lipoprotein phenotype in different categories of patients at higher cardiovascular risk: with coronary and noncoronary forms of atherosclerosis or metabolic diseases, including Type 2 diabetes, polycystic ovary syndrome and growth hormone deficiency. Subjects with higher triglyceride levels, decreased HDL-cholesterol concentrations and increased levels of small, dense LDL (i.e., subjects with the atherogenic lipoprotein phenotype) are common in coronary and noncoronary forms of atherosclerosis. In the future, it may be possible to measure the presence of small, dense LDL to identify subgroups at higher cardiovascular risk.
引用
收藏
页码:553 / 558
页数:6
相关论文
共 24 条
  • [1] ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK
    AUSTIN, MA
    KING, MC
    VRANIZAN, KM
    KRAUSS, RM
    [J]. CIRCULATION, 1990, 82 (02) : 495 - 506
  • [2] Low-density lipoprotein size and subclasses are markers of clinically apparent and non-apparent atherosclerosis in type 2 diabetes
    Berneis, K
    Jeanneret, C
    Muser, E
    Felix, B
    Miserez, AR
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2005, 54 (02): : 227 - 234
  • [3] Atherogenic lipoprotein phenotype and low-density lipoproteins size and subclasses in women with polycystic ovary syndrome
    Berneis, Kaspar
    Rizzo, Manfredi
    Lazzaroni, Veronica
    Fruzzetti, Franca
    Carmina, Enrico
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (01) : 186 - 189
  • [4] Metabolic origins and clinical significance of LDL heterogeneity
    Berneis, KK
    Krauss, RM
    [J]. JOURNAL OF LIPID RESEARCH, 2002, 43 (09) : 1363 - 1379
  • [5] Type 2 diabetes, dyslipidemia, and vascular risk: Rationale and evidence for correcting the lipid imbalance
    Carmena, R
    [J]. AMERICAN HEART JOURNAL, 2005, 150 (05) : 859 - 870
  • [6] Clinical importance and therapeutic modulation of small dense low-density lipoprotein particles
    Gazi, Irene F.
    Tsimihodimos, Vasilis
    Tselepis, Alexandros D.
    Elisaf, Moses
    Mikhailidis, Dimitri P.
    [J]. EXPERT OPINION ON BIOLOGICAL THERAPY, 2007, 7 (01) : 53 - 72
  • [7] Clinical review: Growth hormone and cardiovascular risk factors
    Gola, M
    Bonadonna, S
    Doga, M
    Giustina, A
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (03) : 1864 - 1870
  • [8] 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) Final Report
    Grundy, SM
    Becker, D
    Clark, LT
    Cooper, RS
    Denke, MA
    Howard, WJ
    Hunninghake, DB
    Illingworth, R
    Luepker, RV
    McBride, P
    McKenney, JM
    Pasternak, RC
    Stone, NJ
    Van Horn, L
    Brewer, HB
    Cleeman, JI
    Ernst, ND
    Gordon, D
    Levy, D
    Rifkind, B
    Rossouw, JE
    Savage, P
    Haffner, SM
    Orloff, DG
    Proschan, MA
    Schwartz, JS
    Sempos, CT
    Shero, ST
    Murray, EZ
    Keller, SA
    Jehle, AJ
    [J]. CIRCULATION, 2002, 106 (25) : 3143 - 3421
  • [9] Diagnosis and management of the metabolic syndrome - An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement
    Grundy, SM
    Cleeman, JI
    Daniels, SR
    Donato, KA
    Eckel, RH
    Franklin, BA
    Gordon, DJ
    Krauss, RM
    Savage, PJ
    Smith, SC
    Spertus, JA
    Costa, F
    [J]. CIRCULATION, 2005, 112 (17) : 2735 - 2752
  • [10] KRAUSS RM, 1982, J LIPID RES, V23, P97