Reliability of peripheral arterial tonometry in patients with heart failure, diabetic nephropathy and arterial hypertension

被引:16
|
作者
Weisrock, Fabian [1 ]
Fritschka, Max [2 ]
Beckmann, Sebastian [1 ]
Litmeier, Simon [1 ]
Wagner, Josephine [1 ]
Tahirovic, Elvis [1 ]
Radenovic, Sara [1 ]
Zelenak, Christine [1 ]
Hashemi, Djawid [1 ,3 ]
Busjahn, Andreas [4 ]
Krahn, Thomas [5 ]
Pieske, Burkert [1 ,2 ,3 ]
Dinh, Wilfried [6 ,7 ]
Duengen, Hans-Dirk [1 ]
机构
[1] Charite, Dept Cardiol, Campus Virchow Klinikum, Berlin, Germany
[2] Deutsch Herzzentrum Berlin, Dept Internal Med Cardiol, Berlin, Germany
[3] DZHK German Ctr Cardiovasc Res, Partner Site Berlin, Berlin, Germany
[4] HealthTwiSt GmbH, Berlin, Germany
[5] BAYER Pharma AG, Dept Head Global Biomarker Res, Wuppertal, Germany
[6] Bayer AG, Clin Sci Expt Med, Drug Discovery, Wuppertal, Germany
[7] Univ Hosp Witten Herdecke, Dept Cardiol, HELIOS Clin Wuppertal, Witten, Germany
关键词
EndoPAT; endothelial dysfunction; heart failure; diabetic nephropathy; peripheral arterial tonometry; pulse amplitude tonometry; reactive hyperaemic index; test-retest reliability; VENTRICULAR EJECTION FRACTION; TEST-RETEST RELIABILITY; INCREMENTAL PROGNOSTIC-SIGNIFICANCE; ENDOTHELIAL FUNCTION; NITRIC-OXIDE; DYSFUNCTION; REPRODUCIBILITY; AMPLITUDE; DISEASE; RISK;
D O I
10.1177/1358863X17706752
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Endothelial dysfunction plays a major role in cardiovascular diseases and pulse amplitude tonometry (PAT) offers a non-invasive way to assess endothelial dysfunction. However, data about the reliability of PAT in cardiovascular patient populations are scarce. Thus, we evaluated the test-retest reliability of PAT using the natural logarithmic transformed reactive hyperaemia index (LnRHI). Our cohort consisted of 91 patients (mean age: 65 +/- 9.7 years, 32% female), who were divided into four groups: those with heart failure with preserved ejection fraction (HFpEF) (n=25), heart failure with reduced ejection fraction (HFrEF) (n=22), diabetic nephropathy (n=21), and arterial hypertension (n=23). All subjects underwent two separate PAT measurements at a median interval of 7 days (range 4-14 days). LnRHI derived by PAT showed good reliability in subjects with diabetic nephropathy (intra-class correlation (ICC) = 0.863) and satisfactory reliability in patients with both HFpEF (ICC = 0.557) and HFrEF (ICC = 0.576). However, in subjects with arterial hypertension, reliability was poor (ICC = 0.125). We demonstrated that PAT is a reliable technique to assess endothelial dysfunction in adults with diabetic nephropathy, HFpEF or HFrEF. However, in subjects with arterial hypertension, we did not find sufficient reliability, which can possibly be attributed to variations in heart rate and the respective time of the assessments. Clinical Trial Registration Identifier: NCT02299960.
引用
收藏
页码:292 / 300
页数:9
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