DETECTION OF EARLY SYMPATHETIC CARDIOVASCULAR NEUROPATHY BY SQUATTINGTEST IN NIDDM

Citation
R. Marfella et al., DETECTION OF EARLY SYMPATHETIC CARDIOVASCULAR NEUROPATHY BY SQUATTINGTEST IN NIDDM, Diabetes care, 17(2), 1994, pp. 149-151
Citations number
11
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
Journal title
ISSN journal
01495992
Volume
17
Issue
2
Year of publication
1994
Pages
149 - 151
Database
ISI
SICI code
0149-5992(1994)17:2<149:DOESCN>2.0.ZU;2-1
Abstract
OBJECTIVE - To determine the role of the squatting test in the detecti on of early sympathetic neuropathy in patients with non-insulin-depend ent diabetes mellitus (NIDDM). RESEARCH DESIGN AND METHODS - Three gro ups of nonsmoking, nonobese subjects were studied: 10 healthy subjects , 10 NIDDM patients without autonomic neuropathy (AN), and 10 NIDDM pa tients with AN defined by the presence of a pathological deep-breathin g value. All subjects were given three postural tests: lying-to-standi ng, sitting-to-standing, and squatting test. Heart rate (HR) and finge r arterial pressure were recorded with a noninvasive technique. RESULT S - Blood pressure (BP) fall (expressed as decremental area) was not s ignificantly different among the groups at standing up after sitting o r lying. By contrast, a significantly greater BP drop occurred in NIDD M patients with AN (1,123 +/- 245 mm2) compared with NIDDM patients wi thout AN (460 +/- 232 mm2) or normal subjects (429 +/- 138 mm2, P < 0. 001). The HR increase after all the orthostatic maneuvers was smaller in diabetic patients with AN (P < 0.01) compared with that recorded in other groups. Significant correlations were observed between BP fall after squatting and either the expiration:inspiration ratio at deep br eathing (r = -0.77, P < 0.001) or the duration of diabetes (r = 0.76, P < 0.001). CONCLUSIONS - The intrinsic orthostatic load of the squatt ing test, which is greater than conventional postural maneuvers, makes the squatting test an easy and useful test to detect early orthostati c dysregulation in NIDDM.