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. 2020 Jan 23;7(2):493–502. doi: 10.1002/ehf2.12593

Table 1.

Clinicopathological data

Non‐failing hearts (n = 20) DCM (n = 75)
Mean ± SD or n Limits Mean ± SD or n Limits Correlation with %5‐mC+ cardiomyocyte
r value P value
Clinical data
Age (year old) 56 ± 17 14–77 58 ± 14 17‐81 −0.0661 0.5730
Gender (M/F) 11/9 51/24
LVSP (mm Hg) 137 ± 29 100–200 135 ± 25 75–200 −0.0314 0.7892
LVEDP (mm Hg) 13 ± 5.9 4–25 16 ± 8.2 4–40 0.2397 0.0397
Heart rate (bpm) 68 ± 13 47–94 77 ± 16* 53–132 0.2391 0.0388
LVEF (%) 64 ± 6 55–76 38 ± 10* 10–54 −0.2917 0.0111
LVEDVI (ml/m2) 90 ± 19 57–135 124 ± 39* 30–222 0.2442 0.0347
LVESVI (ml/m2) 32 ± 10 12–57 78 ± 33* 15–169 0.3136 0.0062
LVMI (g/m2) 101 ± 42 57–206 137 ± 41* 65–248 0.2287 0.0484
Histological data
Cardiomyocyte size (μm) 17 ± 2.6 12.8–21.8 26 ± 4.7* 13.9–40.3 0.0248 0.8325
Degree of fibrosis (0–3) 1.0 ± 0.7 0–2 1.7 ± 0.7* 0.5–3 0.0296 0.8009
Inflammatory cells (per HPF) 0.4 ± 0.5 0–1 0.9 ± 0.6* 0–2 0.0513 0.6621
Cardiomyocyte population (%)a 33 ± 5.3 24–38 23 ± 3.6* 18–28

LVSP and LVEDP, left ventricular peak systolic and end‐diastolic pressure; LVEDVI and LVESVI, left ventricular end‐diastolic and end‐systolic volume index; LVEF, left ventricular ejection fraction; LVMI, left ventricular mass index; HPF, high power field.

*

P < 0.05 vs. non‐failing hearts.

a

n = 6 in each group.