USE OF SERUM CREATINE-KINASE MM ISOFORMS FOR PREDICTING THE PROGRESSION OF LEFT-VENTRICULAR DILATION IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHY

Citation
K. Hina et al., USE OF SERUM CREATINE-KINASE MM ISOFORMS FOR PREDICTING THE PROGRESSION OF LEFT-VENTRICULAR DILATION IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHY, Japanese Circulation Journal, 61(4), 1997, pp. 315-322
Citations number
23
Categorie Soggetti
Peripheal Vascular Diseas
ISSN journal
00471828
Volume
61
Issue
4
Year of publication
1997
Pages
315 - 322
Database
ISI
SICI code
0047-1828(1997)61:4<315:UOSCMI>2.0.ZU;2-E
Abstract
Serum creatine kinase (CK) isoforms were examined to detect the progre ssion of left ventricular (LV) enlargement with reduced motion, resemb ling dilated cardiomyopathy (DCM), in hypertrophic cardiomyopathy (HCM ). Changes in LV indices were determined annually by echocardiography in 51 patients until serum measurements (first follow-up period, 6.5+/ -2.2 years). Serum creatine isoforms (CKMM1, CKMM2 and CKMM3) were mea sured with high-voltage electrophoresis in 35 of these patients from 1 991 to 1992, and the data for these latter patients are reported here. Serum total CK, CKMB, lactate dehydrogenase and its isoenzyme LDH1 we re also measured. The changes in LV indices were further monitored unt il January, 1995 (second follow-up). During the 2 follow-up periods, t he patients in the on-going group showed a reduction in the LV ejectio n fraction (LVEF) to <55% with LV end-diastolic dimension (LVDd) <55 m m, and those in the DCM-like group showed a reduction in LVEF to <55% and an increase in LVDd to greater than or equal to 55 mm. During the first follow-up period, LVEF and LVDd remained at greater than or equa l to 55% and <55 mm, respectively, in 26 patients (nonprogressive-dise ase group), while 3 patients entered the on-going group and 6 entered the DCM-like group. The CKMM3/CKMM1 ratios in the on-going and DCM-lik e groups were significantly higher than those in the control and nonpr ogressive-disease groups. The CKMM3/CKMM1 ratio was significantly corr elated with the annual rate of change for the LV end-systolic dimensio n (LVDs), LVDd, and LVEF, with the closest correlation observed for th e annual change in LVDs. Moreover, 5 patients in the nonprogressive-di sease group with elevation of the CKMM3/CKMM1 ratio to >+2SD above the mean for the controls had an elevated annual change in LVDs within +/ -1SD of the mean in the DCM-like group. These results indicate that th e ratio of CKMM3 to CKMM1 can be used to predict the progression of LV enlargement in HCM.