Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 1995;92:364-370

This Article
Right arrow Full Text
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Syvänne, M.
Right arrow Articles by Taskinen, M.-R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Syvänne, M.
Right arrow Articles by Taskinen, M.-R.

(Circulation. 1995;92:364-370.)
© 1995 American Heart Association, Inc.


Articles

HDLs Containing Apolipoproteins A-I and A-II (LpA-I:A-II) as Markers of Coronary Artery Disease in Men With Non–Insulin- Dependent Diabetes Mellitus

Mikko Syvänne, MD; Juhani Kahri, MD; Kari S. Virtanen, MD; Marja-Riitta Taskinen, MD

From the First (M.S., K.S.V.) and Third (J.K., M-R.T.) Departments of Medicine, Helsinki (Finland) University Central Hospital.

Correspondence and reprint requests to Dr Mikko Syvänne, First Department of Medicine, Helsinki University Central Hospital, Haartmaninkatu 4, FIN-00290 Helsinki, Finland.

Background Abnormalities in HDL and an increased risk of coronary artery disease (CAD) coexist in non–insulin-dependent diabetes mellitus (NIDDM). HDLs can be separated by their apolipoprotein (apo) content into particles containing apoA-I but not apoA-II (LpA-I) and those containing both apoA-I and apoA-II (LpA-I:A-II). The LpA-I particles have been suggested to be more effective in conferring protection against CAD than the LpA-I:A-II particles. However, data are sparse, and no studies have defined the role of these two classes of particles in NIDDM.

Methods and Results LpA-I and LpA-I:A-II particles were quantified by a differential electroimmunoassay in four groups of men with similar age and body mass index (BMI) distributions. Group 1 consisted of 50 patients with NIDDM and angiographically verified CAD; group 2, 50 men with CAD but no diabetes; group 3, 50 men with NIDDM but no CAD; and group 4, 31 healthy men. Serum apoA-I and apoA-II concentrations were measured by immunoturbidimetry, and HDL2 and HDL3 were separated by ultracentrifugation. Concentrations of LpA-I:A-II particles in group 1 were 13.8%, 18.3%, and 26.9% lower than in groups 2 through 4, respectively. In a two-by-two factorial ANOVA, adjusted for age and BMI, the differences were significant for both CAD (P<.001) and NIDDM (P<.001), with no interaction between the factors. These results were confirmed by comparable differences in the serum concentrations of apoA-I and apoA-II. LpA-I particles were related to the presence or absence of CAD (P=.013), but the difference was lost in a multivariate analysis. A low HDL3 cholesterol concentration characterized both CAD (P=.002) and NIDDM (P=.024). HDL2 cholesterol differed significantly with regard to the presence of NIDDM (P=.033) but only borderline with respect to CAD (P=.073).

Conclusions ApoA-II–containing lipoproteins and HDL3 cholesterol are powerful markers of CAD in men with NIDDM.


Key Words: diabetes mellitus • lipoproteins • risk factors




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
C. Wolfrum, J. J. Howell, E. Ndungo, and M. Stoffel
Foxa2 Activity Increases Plasma High Density Lipoprotein Levels by Regulating Apolipoprotein M
J. Biol. Chem., June 13, 2008; 283(24): 16940 - 16949.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
E. M. M. Ooi, G. F. Watts, P. J. Nestel, D. Sviridov, A. Hoang, and P. H. R. Barrett
Dose-Dependent Regulation of High-Density Lipoprotein Metabolism with Rosuvastatin in the Metabolic Syndrome
J. Clin. Endocrinol. Metab., February 1, 2008; 93(2): 430 - 437.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
R. S. Birjmohun, G. M. Dallinga-Thie, J. A. Kuivenhoven, E. S.G. Stroes, J. D. Otvos, N. J. Wareham, R. Luben, J. J.P. Kastelein, K.-T. Khaw, and S. M. Boekholdt
Apolipoprotein A-II Is Inversely Associated With Risk of Future Coronary Artery Disease
Circulation, October 30, 2007; 116(18): 2029 - 2035.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
J. Ji, G. F. Watts, A. G. Johnson, D. C. Chan, E. M. M. Ooi, K.-A. Rye, A. P. Serone, and P. H. R. Barrett
High-Density Lipoprotein (HDL) Transport in the Metabolic Syndrome: Application of a New Model for HDL Particle Kinetics
J. Clin. Endocrinol. Metab., March 1, 2006; 91(3): 973 - 979.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
G. Luc, J.-M. Bard, J. Ferrieres, A. Evans, P. Amouyel, D. Arveiler, J.-C. Fruchart, P. Ducimetiere, and on behalf of the PRIME Study Group
Value of HDL Cholesterol, Apolipoprotein A-I, Lipoprotein A-I, and Lipoprotein A-I/A-II in Prediction of Coronary Heart Disease: The PRIME Study
Arterioscler. Thromb. Vasc. Biol., July 1, 2002; 22(7): 1155 - 1161.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
K. Miwa, N. Yoshida, K. Nakagawa, and H. Inoue
High-density lipoprotein particles are large in patients with variant angina
Cardiovasc Res, March 1, 1998; 37(3): 729 - 737.
[Abstract] [Full Text] [PDF]