USEFULNESS OF PLASMA BETA-ENDORPHIN LEVEL, PAIN THRESHOLD AND AUTONOMIC FUNCTION IN ASSESSING SILENT-MYOCARDIAL-ISCHEMIA IN PATIENTS WITH AND WITHOUT DIABETES-MELLITUS
Citation
H. Hikita et al., USEFULNESS OF PLASMA BETA-ENDORPHIN LEVEL, PAIN THRESHOLD AND AUTONOMIC FUNCTION IN ASSESSING SILENT-MYOCARDIAL-ISCHEMIA IN PATIENTS WITH AND WITHOUT DIABETES-MELLITUS, The American journal of cardiology, 72(2), 1993, pp. 140-143
Categorie Soggetti
Cardiac & Cardiovascular System
SICI code
0002-9149(1993)72:2<140:UOPBLP>2.0.ZU;2-3
Abstract
The differences between diabetic and nondiabetic Patients with silent
myocardial ischemia were investigated. Based on the results of previou
s exercise testing, a total of 110 patients (15 diabetic and 95 nondia
betic) with exercise-induced myocardial ischemia were divided into the
following 3 groups: 15 diabetics with silent myocardial ischemia, 49
nondiabetics with silent myocardial ischemia, and 46 nondiabetics with
anginal symptoms. All patients underwent treadmill exercise testing a
nd 24-hour ambulatory electrocardiographic recording. Before and durin
g exercise, blood samples from the antecubital vein were obtained to d
etermine the beta-endorphin levels, and the pain threshold of each pat
ient was measured with the electrical skin stimulation test. Furthermo
re, with regard to the ambulatory electrocardiographic recording, the
mean of the SDs of all normal sinus RR intervals during successive 5-m
inute recording periods over 24 hours was analyzed and considered as a
n index of the autonomic function. The beta-endorphin level during exe
rcise was significantly greater in nondiabetic patients with silent is
chemia than in diabetic ones. The SD mean was significantly less in th
e diabetic group than in the 2 nondiabetic ones. The findings suggest
that the role of beta endorphin in diabetic patients with silent myoca
rdial ischemia may be less significant than in nondiabetic ones; there
fore, a diabetic neuropathy that affects the autonomic pain fibers tha
t innervate the heart may be involved in the mechanism of silent myoca
rdial ischemia in diabetics.