Effect of family history of type-2 diabetes on coronary flow reserve and it's relationship with insulin resistance: an observational study

被引:2
作者
Caliskan, Mustafa [1 ]
Pamuk, Baris Onder [2 ]
Gullu, Hakan [1 ]
Ciftci, Ozgur [1 ]
Caliskan, Zuhal [3 ]
Erdogan, Dogan [1 ]
Guven, Aytekin [1 ]
Polat, Ezgi [1 ]
Muderrisoglu, Haldun [1 ]
机构
[1] Baskent Univ, Dept Cardiol, Fac Med, TR-06490 Ankara, Turkey
[2] Baskent Univ, Fac Med, Dept Endocrinol, TR-06490 Ankara, Turkey
[3] Baskent Univ, Fac Med, Dept Internal Med, TR-06490 Ankara, Turkey
关键词
Coronary flow reserve; diabetes; heritage; regression analysis; CARDIOVASCULAR-DISEASE; GLUCOSE-TOLERANCE; PLASMA-GLUCOSE; BLOOD-GLUCOSE; HEART-DISEASE; RISK; MORTALITY;
D O I
10.5152/akd.2013.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Coronary microvascular function among offspring of patients with diabetes mellitus might be compromised when compared to persons with no first-degree relative with diabetes mellitus. The aim of the study was to evaluate effect of family history of type-2 diabetes on coronary flow reserve. Methods: In this observational study, we evaluated coronary flow reserve (CFR) via echocardiography of 95 subjects having a biological parent with type-2 diabetes and 34 healthy volunteers without any biological parent with type-2 diabetes. We have analyzed possible association with CFR and homeostasis model assessment - insulin resistance (HOMA-IR). Comparison analyses were made using independent samples t test, Chi-square test and one-way ANOVA. Association of independent variables with CFR was obtained by correlation analysis and stepwise linear regression model including potential confounders. Results: CFR was significantly lower in the positive family history group than in the controls. Moreover, when compared with controls, the subgroup of insulin-sensitive subjects in the positive family history group also had significantly reduced CFR (2.67 +/- 0.28 vs. 2.83 +/- 0.19; p=0.01). Correlation analysis revealed that CFR was inversely correlated with HOMA-IR, (r=-0.433), fasting glucose (r=-0.331), fasting insulin (r=-0.396), and hemoglobin (Hb)A1c (r=-0.405). When the positive family history group was divided into tertiles of insulin resistance (HOMAIR <1.3, 1.3-2.6, and >2.6; Groups 1-2, and 3), there was a significant difference in CFR between Groups 1 and 2 and between Groups 1 and 3 (p<0.05 for all). Though statistically not significant, there was also a difference in CFR between Groups 2 and 3. In a linear regression model, only fasting glucose level was independent predictor of CFR (beta=-677; p value =0.001, 95% CI: -0.061 and -0.019). Conclusion: Nondiabetic first-degree relatives of patients with type-2 diabetes are at increased risk of developing coronary microvascular dysfunction. (Anadolu Kardiyol Derg 2013; 13: 48-56)
引用
收藏
页码:48 / 56
页数:9
相关论文
共 25 条
[1]   High blood glucose concentration is a risk factor for mortality in middle-aged nondiabetic men -: 20-year follow-up in the Whitehall Study, the Paris Prospective Study, and the Helsinki Policemen Study [J].
Balkau, B ;
Shipley, M ;
Jarrett, RJ ;
Pyörälä, K ;
Pyörälä, M ;
Forhan, A ;
Eschwège, E .
DIABETES CARE, 1998, 21 (03) :360-367
[2]   METABOLIC AND GENETIC-CHARACTERIZATION OF PREDIABETIC STATES - SEQUENCE OF EVENTS LEADING TO NON-INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BECKNIELSEN, H ;
GROOP, LC .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :1714-1721
[3]   Novel clinical markers of vascular wall inflammation [J].
Blake, GJ ;
Ridker, PM .
CIRCULATION RESEARCH, 2001, 89 (09) :763-771
[4]   A1C Is Associated With Intima-Media Thickness in Individuals With Normal Glucose Tolerance [J].
Bobbert, Thomas ;
Mai, Knut ;
Fischer-Rosinsky, Antje ;
Pfeiffer, Andreas F. H. ;
Spranger, Joachim .
DIABETES CARE, 2010, 33 (01) :203-204
[5]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[6]   Microvascular and macrovascular reactivity is reduced in subjects at risk for type 2 diabetes [J].
Caballero, AE ;
Arora, S ;
Saouaf, R ;
Lim, SC ;
Smakowski, P ;
Park, JY ;
King, GL ;
LoGerfo, FW ;
Horton, ES ;
Veves, A .
DIABETES, 1999, 48 (09) :1856-1862
[7]   ECHOCARDIOGRAPHIC DETERMINATION OF LEFT-VENTRICULAR MASS IN MAN - ANATOMIC VALIDATION OF METHOD [J].
DEVEREUX, RB ;
REICHEK, N .
CIRCULATION, 1977, 55 (04) :613-618
[8]   The non-invasive documentation of coronary microcirculation impairment: Role of transthoracic echocardiography [J].
Dimitrow P.P. ;
Galderisi M. ;
Rigo F. .
Cardiovascular Ultrasound, 3 (1)
[9]  
ESCHWEGE E, 1985, HORM METAB RES, V15, P41
[10]   Chronic subclinical inflammation as part of the insulin resistance syndrome -: The Insulin Resistance Atherosclerosis Study (IRAS) [J].
Festa, A ;
D'Agostino, R ;
Howard, G ;
Mykkänen, L ;
Tracy, RP ;
Haffner, SM .
CIRCULATION, 2000, 102 (01) :42-47