TY - JOUR
T1 - Paradoxical increase in ventricular torsion and systolic torsion rate in type i diabetic patients under tight glycemic control
AU - Chung, Jina
AU - Abraszewski, Paul
AU - Yu, Xin
AU - Liu, Wei
AU - Krainik, Andrew J.
AU - Ashford, Marvin
AU - Caruthers, Shelton D.
AU - McGill, Janet B.
AU - Wickline, Samuel A.
PY - 2006/1/17
Y1 - 2006/1/17
N2 - OBJECTIVES: This study sought to characterize the early features of diabetic cardiomyopathy by magnetic resonance imaging (MRI) tagging. BACKGROUND: The earliest manifestations of diabetic cardiomyopathy have not been well established, especially under tight glycemic management. We hypothesized that torsion measurements would identify subclinical contractile alterations in type I diabetics with normal left ventricular ejection fraction, mass, blood pressure, and aggressive glycemic control. We also sought to characterize the influence of elevated resting heart rates (HRs) of diabetics on torsion. METHODS: Sixteen patients with type I diabetes and 10 control patients underwent cine and tagged MRI with a 1.5-T scanner. Torsion, strain, and their rates were measured. To quantify the influence of chronotropic and inotropic stimulation on torsion, nine healthy volunteers underwent MRI tagging at rest, after atropine injection, and after exercise. RESULTS: Diabetic patients (hemoglobin A1c, 6.8 ± 0.4%) had a higher resting HR (77.0 ± 12.4 beats/min vs. 59.0 ± 5.6 beats/min; p < 0.01), higher maximal torsion by 23% (3.5 ± 0.9°/cm vs. 2.7 ± 0.4°/cm; p < 0.01) and higher maximal systolic torsion rate (TR-s) by 25% (0.013 ± 0.003°/cm/s vs. 0.010 ± 0.002°/cm/s, p = 0.01). Torsion did not significantly change with chronotropic stimulation (p = 0.30). CONCLUSIONS: In diabetics under tight glycemic control, we observed a surprising increase in torsion and TR-s unrelated to chronotropic influences of HR. We propose that increased torsion and TR-s could represent early predictive markers of the propensity to cardiac dysfunction in asymptomatic type I diabetics. Furthermore, these findings seem fundamental to the diabetic state itself and unaccounted for by other comorbidities.
AB - OBJECTIVES: This study sought to characterize the early features of diabetic cardiomyopathy by magnetic resonance imaging (MRI) tagging. BACKGROUND: The earliest manifestations of diabetic cardiomyopathy have not been well established, especially under tight glycemic management. We hypothesized that torsion measurements would identify subclinical contractile alterations in type I diabetics with normal left ventricular ejection fraction, mass, blood pressure, and aggressive glycemic control. We also sought to characterize the influence of elevated resting heart rates (HRs) of diabetics on torsion. METHODS: Sixteen patients with type I diabetes and 10 control patients underwent cine and tagged MRI with a 1.5-T scanner. Torsion, strain, and their rates were measured. To quantify the influence of chronotropic and inotropic stimulation on torsion, nine healthy volunteers underwent MRI tagging at rest, after atropine injection, and after exercise. RESULTS: Diabetic patients (hemoglobin A1c, 6.8 ± 0.4%) had a higher resting HR (77.0 ± 12.4 beats/min vs. 59.0 ± 5.6 beats/min; p < 0.01), higher maximal torsion by 23% (3.5 ± 0.9°/cm vs. 2.7 ± 0.4°/cm; p < 0.01) and higher maximal systolic torsion rate (TR-s) by 25% (0.013 ± 0.003°/cm/s vs. 0.010 ± 0.002°/cm/s, p = 0.01). Torsion did not significantly change with chronotropic stimulation (p = 0.30). CONCLUSIONS: In diabetics under tight glycemic control, we observed a surprising increase in torsion and TR-s unrelated to chronotropic influences of HR. We propose that increased torsion and TR-s could represent early predictive markers of the propensity to cardiac dysfunction in asymptomatic type I diabetics. Furthermore, these findings seem fundamental to the diabetic state itself and unaccounted for by other comorbidities.
UR - http://www.scopus.com/inward/record.url?scp=30344469097&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2005.08.061
DO - 10.1016/j.jacc.2005.08.061
M3 - Article
C2 - 16412865
AN - SCOPUS:30344469097
SN - 0735-1097
VL - 47
SP - 384
EP - 390
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 2
ER -