Skip to main content
. 2014 Sep 16;16(1):66. doi: 10.1186/s12968-014-0066-0

Table 2.

Crypt prevalence

Patients without crypts Patients with crypts Patients with partial crypts
Overall prevalence n- (%) 927 (90.9%) 64(6.3%) 29 (2.8%)
Age- years (SD) 52.5 (17.0) 53.23 (16.2) 54.9 (16.7)
Gender male/female (% male) 565/362 (61%) 42/22 (66%) 15/14 (52%)
Final Diagnosis- n (%)
ICM 214 (90.7%) 12 (5.1%) 10 (4.2%)
NICM 342 (91.0%) 24 (6.4%) 10 (2.7%)
DCM 120 (95.3%) 5 (3.9%) 1 (0.8%)
HtCM 8 (73%) 3 (27%)* 0
Inflammatory CM 79 (89.8%) 5 (5.7%) 4 (4.5%)
HCM 67 (87%) 9 (11.7)* 1 (1.3%)
ARVC 2 (50%) 0 2 (50%)
Congenital 4 (67%) 0 2 (33%)
Pericardial disease 7 0
Other/ 55 2
Phenotype negative inherited cardiomyopathy family members (including HCM) 31 (72.1%) 10 (23.3%)** 2 (4.7%)
Phenotype negative HCM family members 6 (67%) 3 (33%)* 0
‘Control’ group 295 (96%) 11 (3.6%)*
Unknown 45 (79%) 5 (8.8%) 7 (12.2%)

Distribution of Crypts by gender, age and clinical diagnosis. Crypts >50% invagination into surrounding normal myocardium. Partial crypts 25-50% invagination. ICM – ischemic cardiomyopathy, NICM – non-ischemic cardiomyopathy, DCM – dilated cardiomyopathy, HtCM – hypertensive cardiomyopathy, HCM – hypertrophic cardiomyopathy, ARVC – arrhythmogenic right ventricular cardiomyopathy. T-tests performed between crypts > 50% group and no crypt group. *p < 0.05, **p < 0.01.