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Plasma apolipoprotein M responses to statin and fibrate administration in type 2 diabetes mellitus

Kappelle, Paul J. W. H. (author)
Ahnström, Josefin (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups
Dikkeschei, Bert D. (author)
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de Vries, Rindert (author)
Sluiter, Wim J. (author)
Wolffenbuttel, Bruce H. R. (author)
van Tol, Arie (author)
Nielsen, Lars Bo (author)
Dahlbäck, Björn (author)
Lund University,Lunds universitet,Klinisk kemi, Malmö,Forskargrupper vid Lunds universitet,Clinical Chemistry, Malmö,Lund University Research Groups
Dullaart, Robin P. F. (author)
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 (creator_code:org_t)
Elsevier BV, 2010
2010
English.
In: Atherosclerosis. - : Elsevier BV. - 1879-1484 .- 0021-9150. ; 213:1, s. 247-250
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose: Plasma apolipoprotein M (apoM) is potentially anti-atherogenic, and has been found to be associated positively with plasma total, LDL and HDL cholesterol in humans. ApoM may, therefore, be intricately related to cholesterol metabolism. Here, we determined whether plasma apoM is affected by statin or fibrate administration in patients with diabetes mellitus. Methods: Fourteen type 2 diabetic patients participated in a placebo-controlled crossover study which included three 8-week treatment periods with simvastatin (40 mg daily), bezafibrate (400 mg daily), and their combination. Results: ApoM was decreased by 7% in response to simvastatin (P < 0.05 from baseline and placebo), and remained unchanged during bezafibrate and combined simvastatin + bezafibrate administration. Plasma apoM concentrations correlated positively with apoB-containing lipoprotein measures at baseline and during placebo (P < 0.02 to P < 0.001), but these relationships were lost during all lipid lowering treatment periods. Conclusions: This study suggests that, even though plasma apoM is lowered by statins, apoM metabolism is to a considerable extent independent of statin-and fibrate-affected pathways involved in cholesterol homeostasis. (C) 2010 Elsevier Ireland Ltd. All rights reserved.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

LDL
HDL cholesterol
Bezafibrate
Apolipoprotein M
Apolipoprotein B
cholesterol
Simvastatin
Type 2 diabetes

Publication and Content Type

art (subject category)
ref (subject category)

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