Improved Preservation of Residual Beta Cell Function by Atorvastatin in Patients with Recent Onset Type 1 Diabetes and High CRP Levels (DIATOR Trial)

被引:17
作者
Strom, Alexander [1 ]
Kolb, Hubert [2 ]
Martin, Stephan [3 ]
Herder, Christian [1 ]
Simon, Marie-Christine [1 ]
Koenig, Wolfgang [4 ]
Heise, Tim [5 ]
Heinemann, Lutz [5 ]
Roden, Michael [1 ,6 ]
Schloot, Nanette C. [1 ,6 ]
机构
[1] Univ Dusseldorf, Leibniz Ctr Diabet Res, German Diabet Ctr, Inst Clin Diabetol, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Univ Hosp, Immunobiol Res Grp, D-40225 Dusseldorf, Germany
[3] Verbund Katholischer Kliniken Dusseldorf, W German Ctr Diabet & Hlth, Dusseldorf, Germany
[4] Univ Ulm, Med Ctr, Dept Internal Med Cardiol 2, Ulm, Germany
[5] Profil Inst Metab Res, Neuss, Germany
[6] Univ Hosp, Dept Metab Dis, Dusseldorf, Germany
关键词
ACUTE-PHASE PROTEINS; C-REACTIVE PROTEIN; STATINS; ACTIVATION; REDUCTASE; RECEPTOR; INFLAMMATION; TOLERANCE; DIAGNOSIS; DISEASE;
D O I
10.1371/journal.pone.0033108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: A recent randomized placebo-controlled trial of the effect of atorvastatin treatment on the progression of newly diagnosed type 1 diabetes suggested a slower decline of residual beta cell function with statin treatment. Aim of this secondary analysis was to identify patient subgroups which differ in the decline of beta cell function during treatment with atorvastatin. Methodology/Principal Findings: The randomized placebo-controlled Diabetes and Atorvastatin (DIATOR) Trial included 89 patients with newly diagnosed type 1 diabetes and detectable islet autoantibodies (mean age 30 years, 40% females), in 12 centers in Germany. Patients received placebo or 80 mg/d atorvastatin for 18 months. As primary outcome stimulated serum C-peptide levels were determined 90 min after a standardized liquid mixed meal. For this secondary analysis patients were stratified by single baseline characteristics which were considered to possibly be modified by atorvastatin treatment. Subgroups defined by age, sex or by baseline metabolic parameters like body mass index (BMI), total serum cholesterol or fasting C-peptide did not differ in C-peptide outcome after atorvastatin treatment. However, the subgroup defined by high (above median) baseline C-reactive protein (CRP) concentrations exhibited higher stimulated C-peptide secretion after statin treatment (p = 0.044). Individual baseline CRP levels correlated with C-peptide outcome in the statin group (r(2) = 0.3079, p<0.004). The subgroup with baseline CRP concentrations above median differed from the corresponding subgroup with lower CRP levels by higher median values of BMI, IL-6, IL-1RA, sICAM-1 and E-selectin. Conclusions/Significance: Atorvastatin treatment may be effective in slowing the decline of beta cell function in a patient subgroup defined by above median levels of CRP and other inflammation associated immune mediators.
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页数:6
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