Influencing factors on cardiac structure and function beyond glycemic control in patients with type 2 diabetes mellitus

被引:34
作者
Ichikawa, Ryoko [1 ]
Daimon, Masao [1 ]
Miyazaki, Tetsuro [1 ]
Kawata, Takayuki [1 ]
Miyazaki, Sakiko [1 ]
Maruyama, Masaki [1 ]
Chiang, Shuo-Ju [1 ]
Suzuki, Hiromasa [1 ]
Ito, Chiharu [2 ]
Sato, Fumihiko [2 ]
Watada, Hirotaka [2 ]
Daida, Hiroyuki [1 ]
机构
[1] Juntendo Univ, Sch Med, Dept Cardiovasc Med, Tokyo 113, Japan
[2] Juntendo Univ, Sch Med, Dept Metab & Endocrinol, Bunkyo Ku, Tokyo 1138421, Japan
基金
日本学术振兴会;
关键词
Diabetes mellitus; Echocardiography; Cardiac function; VENTRICULAR DIASTOLIC DYSFUNCTION; INSULIN-RESISTANCE; GENETIC EPIDEMIOLOGY; HEART-FAILURE; CARDIOMYOPATHY; ADIPOSITY; RECOMMENDATIONS; METAANALYSIS; ASSOCIATION; ADIPONECTIN;
D O I
10.1186/1475-2840-12-38
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: We hypothesized that clinical factors other than glycemic control may influence abnormal cardiac function in patients with type 2 diabetes mellitus (T2DM). We aimed to investigate the independent factors for abnormal cardiac function among clinical factors in T2DM. Methods: We studied 148 asymptomatic patients with T2DM without overt heart disease. Echocardiographic findings were compared between diabetic patients and 68 age-matched healthy subjects. Early (E) and late (A) diastolic mitral flow velocity and early diastolic mitral annular velocity (e') were measured for assessing left ventricular (LV) diastolic function. We evaluated insulin resistance, non-esterified fatty acid, high-sensitive CRP, estimated glomerular filtration rate, waist/hip ratio, abdominal visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT) and other clinical characteristics in addition to glycemic control. VAT and SAT were quantified by computed tomography. Results: In T2DM, E/A and e' were significantly lower, and E/e', left atrial volume and LV mass were significantly greater than in control subjects. In multivariate liner regression analysis, VAT was an independent determinant of left atrial volume (beta = 0.203, p = 0.011), E/A (beta = -0.208, p = 0.002), e' (beta = -0.354, p<0.001) and E/e' (beta = 0.220, p = 0.003). Age was also an independent determinant, whereas fasting plasma glucose and hemoglobin A1c levels were not. In addition to systolic blood pressure, waist-hip ratio (beta = 0.173, p = 0.024) and VAT/SAT ratio (beta = 0.162, p = 0.049) were independent determinants of LV mass. Conclusion: Excessive visceral fat accompanied by adipocyte dysfunction may play a greater role than glycemic control in the development of diastolic dysfunction and LV hypertrophy in T2DM.
引用
收藏
页数:9
相关论文
共 43 条
[11]   Subcellular remodeling and heart dysfunction in chronic diabetes [J].
Dhalla, NS ;
Liu, XL ;
Panagia, V ;
Takeda, N .
CARDIOVASCULAR RESEARCH, 1998, 40 (02) :239-247
[12]   Diastolic Dysfunction in Patients with Type 2 Diabetes Mellitus: Is It Really the First Marker of Diabetic Cardiomyopathy? [J].
Ernande, Laura ;
Bergerot, Cyrille ;
Rietzschel, Ernst R. ;
De Buyzere, Marc L. ;
Thibault, Helene ;
PignonBlanc, Pierre Gautier ;
Croisille, Pierre ;
Ovize, Michel ;
Groisne, Laure ;
Moulin, Philippe ;
Gillebert, Thierry C. ;
Derumeaux, Genevieve .
JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 2011, 24 (11) :1268-U147
[13]   The Development of Heart Failure in Patients With Diabetes Mellitus and Pre-Clinical Diastolic Dysfunction A Population-Based Study [J].
From, Aaron M. ;
Scott, Christopher G. ;
Chen, Horng H. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (04) :300-305
[14]   Changes in Diastolic Dysfunction in Diabetes Mellitus Over Time [J].
From, Aaron M. ;
Scott, Christopher G. ;
Chen, Horng H. .
AMERICAN JOURNAL OF CARDIOLOGY, 2009, 103 (10) :1463-1466
[15]   Renal Failure Increases Cardiac Histone H3 Acetylation, Dimethylation, and Phosphorylation and the Induction of Cardiomyopathy-Related Genes in Type 2 Diabetes [J].
Gaikwad, Anil Bhanudas ;
Sayyed, Sufyan G. ;
Lichtnekert, Julia ;
Tikoo, Kulbhushan ;
Anders, Hans-Joachim .
AMERICAN JOURNAL OF PATHOLOGY, 2010, 176 (03) :1079-1083
[16]   Adipose tissue dysfunction in obesity, diabetes, and vascular diseases [J].
Hajer, Gideon R. ;
van Haeften, Timon W. ;
Visseren, Frank L. J. .
EUROPEAN HEART JOURNAL, 2008, 29 (24) :2959-2971
[17]   Intensive glycaemic control for patients with type 2 diabetes: systematic review with meta-analysis and trial sequential analysis of randomised clinical trials [J].
Hemmingsen, Bianca ;
Lund, Soren S. ;
Gluud, Christian ;
Vaag, Allan ;
Almdal, Thomas ;
Hemmingsen, Christina ;
Wetterslev, Jorn .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 343 :1136
[18]   Genetic epidemiology of insulin resistance and visceral adiposity: The IRAS family study design and methods [J].
Henkin, L ;
Bergman, RN ;
Bowden, DW ;
Ellsworth, DL ;
Haffner, SM ;
Langefeld, CD ;
Mitchell, BD ;
Norris, JM ;
Rewers, M ;
Saad, MF ;
Stamm, E ;
Wagenknecht, LE ;
Rich, SS .
ANNALS OF EPIDEMIOLOGY, 2003, 13 (04) :211-217
[19]   ROLE OF DIABETES IN CONGESTIVE HEART-FAILURE - FRAMINGHAM STUDY [J].
KANNEL, WB ;
HJORTLAND, M ;
CASTELLI, WP .
AMERICAN JOURNAL OF CARDIOLOGY, 1974, 34 (01) :29-34
[20]   DIABETES AND CARDIOVASCULAR-DISEASE - FRAMINGHAM-STUDY [J].
KANNEL, WB ;
MCGEE, DL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1979, 241 (19) :2035-2038