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the Egyptian Journal of Internal Medicine ;
Springer nature
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Abstract: |
Background: The relation between metabolic syndrome (M.S.)and the coronary artery disease (CAD) is multifactorial, and the well-known risk factors can explain only about 25% of the disease as the relation between insulin resistance(IR) on top of MS versus severity of CAD still a subject of debate with conflicting data. Also IR and glucose intolerance are included in the definition of metabolic syndrome only by some associations. So the aim of this research was to analyze the the relation between CAD severity (measured by the modified Gensini score) and the different components of the Metabolic Syndrome including insulin resistance and glucose intolerance.
Results: Out of 70 patients enrolled; 71.4 % represented impaired glucose tolerance group (IGT group; n = 50) and 28.6% represented normal Glucose tolerance group (NGT group; n = 20). The following variables were significantly greater among the IGT group including: BMI (30.192.27vs 23.622.92; P< 0.001), waist circumference (105.098.02vs 92.8919.92; P<0.001). frequency of hypertension (80 % vs 50% ; P = 0.012), 2h post prandial glucose (16430 vs 11020; P<0. 04), Fasting insulin (9.21.2 vs 5.1 4. 3; P = 0.003), HOMA-IR (3.030.12 % vs 1.90.12 , P <0.001) , Serum uric acid (4.81.3 vs 5.82.6, P = 0.03 ), mean modified Gensini score (22.39.2 vs 15.46.8, P <0.001 ) , while the mean serum HDL was significantly higher among the NGT group (40.810.1 vs 50.610.2 , P <0.001). There was a positive correlation between HOMA –IR; hs-CRP; M.S.-related variables(including waist circumflex; BMI; serum uric acid; HDL; TG ) ;and the modified Gensini score . (for HOMA, r=0.63 ; P<0.001). Several predictors for high score of modified Gensini were noted in multiple regression analysis, however out of those several predictors; HOMA-IR was the strongest one. (OR = 4.0, 95%CI = (2.04-7.08 ) .
Conclusion: IR is an independent risk factor for CAD severity in patients with IGT and M.S. In patients with IR; those with aggressive CAD (or with a positive family history of premature CAD), IGT should be managed aggressively even before any evidence of frank diabetes. IR work up should be recommended among the other standard workup for those patients, if documented, interventions targeted against IR should be considered among the other standard management.
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