Microvascular effects of the inhibition of dipeptidylpeptidase IV by linagliptin in nondiabetic hypertensive patients

被引:11
作者
Forst, Thomas [1 ,2 ]
Michelson, Georg [3 ]
Diessel, Stephan [1 ]
Jahnke, Johannes [1 ]
Kapitza, Christoph [4 ]
机构
[1] Johannes Gutenberg Univ Mainz, Profil Mainz Rheinstr, Endocrinology Langenbeckstr, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Dept Med 1, Endocrinology Langenbeckstr, Mainz, Germany
[3] Univ Erlangen Nurnberg, Interdisciplinary Ctr Ophthalm Prevent Med & Imag, Erlangen Nuernberg, Germany
[4] Profil Inst Metab Res, Hellersbergstr, Neuss, Germany
关键词
dipeptidylpeptidase-IV inhibition; hypertension; renal function; retinal microvascular blood flow; transforming growth factor beta; TYPE-2; DIABETES-MELLITUS; BLOOD-RETINAL BARRIER; PEPTIDASE-4; INHIBITOR; PRESSURE; SITAGLIPTIN; VILDAGLIPTIN; ALBUMINURIA; METFORMIN; INJURY; GLP-1;
D O I
10.1097/HJH.0000000000000776
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background:Recent studies suggest vascular benefits of dipeptidylpeptidase IV (DPP-IV) inhibition in patients with diabetes mellitus. Only little is known about potential vascular effects of DPP-IV inhibitors in nondiabetic individuals. The aim of this study was to investigate the effect of DPP-IV inhibition in a nondiabetic hypertensive population.Method:This was a double-blinded, randomized, placebo-controlled, mechanistic study, comparing microvascular effects of the DPP-IV inhibitor linagliptin with placebo in nondiabetic individuals with a history of arterial hypertension. Twenty-one patients received 5mg linagliptin (5 women; age 67.66.0 years; meanSD), whereas 22 patients were randomized to placebo (5 women; age 64.8 +/- 7.1 years).Results:At baseline, after 6 and 12 weeks, retinal microcirculation and arterial blood pressure profiles were assessed. Moreover, blood samples were taken for the measurement of HbA1c, asymmetric dimethylarginine, C-reactive peptide, cyclic guanosinmonophosphate, transforming growth factor beta (TGF-ss 1) and cystatin C. Retinal capillary perfusion increased by 23.7 +/- 10.3% (mean +/- SEM; P<0.05), retinal arterial flow by 7.6 +/- 0.6 (P<0.05) and the retinal hyperemic response by 290 +/- 263% (P<0.05) during treatment with linagliptin. No change in retinal blood flow was found in the placebo group. Although blood pressure declined in both groups, a significant decline in TGF-ss 1 by 9.3 +/- 4.5% (P<0.05) could only be observed in the linagliptin group. No significant change in other laboratory parameters could be observed in both groups.Conclusion:Our study suggests microvascular and antifibrotic effects of linagliptin in a nondiabetic, hypertensive population.
引用
收藏
页码:345 / 350
页数:6
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