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  • 标题:Altered lipoprotein subclass distribution and PAF-AH activity in subjects with generalized aggressive periodontitis
  • 作者:Miguel L. Rufail ; Harvey A. Schenkein ; Suzanne E. Barbour
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2005
  • 卷号:46
  • 期号:12
  • 页码:2752-2760
  • DOI:10.1194/jlr.M500389-JLR200
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:In this study, we examined whether the documented increase of plasma triglycerides in patients with generalized aggressive periodontitis (GAgP) is associated with changes in lipoprotein subclass distribution and/or LDL-associated platelet-activating factor acetylhydrolase (PAF-AH) activity. Lipoprotein subclasses were analyzed in whole plasma samples using nuclear magnetic resonance methods. Compared with subjects without periodontitis (NP subjects; n = 12), GAgP subjects (n = 12) had higher plasma levels of large, medium, and small VLDL (35.0 ± 6.7 vs. 63.1 ± 9.6 nmol/l; P = 0.025), higher levels of intermediate density lipoprotein (24.8 ± 11.6 vs. 87.2 ± 16.6 nmol/l; P = 0.006), lower levels of large LDL (448.3 ± 48.5 vs. 315.8 ± 59.4 nmol/l; P = 0.098), and higher levels of small LDL (488.2 ± 104.2 vs. 946.7 ± 151.6 nmol/l; P = 0.021). The average size of LDL from NP and GAgP subjects was 21.4 ± 0.2 and 20.6 ± 0.3 nm, respectively ( P = 0.031). Compared with NP subjects, GAgP subjects had a greater number of circulating LDL particles (961.3 ± 105.3 vs. 1,349.0 ± 133.2 nmol/l; P = 0.032). Differences in the plasma levels of large, medium, and small HDL were not statistically significant. NP and GAgP subjects had similar plasma levels of total LDL-associated PAF-AH activity; however, LDL of GAgP subjects contained less PAF-AH activity per microgram of LDL protein (1,458.0 ± 171.0 and 865.2 ± 134 pmol/min/μg; P = 0.014). These results indicate that, in general, GAgP subjects have a more atherogenic lipoprotein profile and lower LDL-associated PAF-AH activity than NP subjects. These differences may help explain the increased risk of GAgP subjects for cardiovascular disease.
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