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. 2019 Sep;31(3):241–245. doi: 10.4314/mmj.v31i3.14

Table 2.

Individual studies with sample sizes and types of cardiomyopathy

Study Sample
size
CMR Findings
Goebel et al.18
2016
150 T1 mapping
CMR
Does not differentiate healthy
and diffusely diseased
myocardium
Makoto et al.19
2016
44 LGE CMR LE in CS predominantly
basal, mid septum and
throughout the LV, while in
DCM, LE was localized in the
basal and mid septum
Mikami et al.20
2016
118 LGE CMR Septal fibrosis
Okada et al.21
2016
102 LGE CMR TIC had a significant lower
RVEF, and a larger RVEDV
and RVEDS
Kwong et al.22
2015
81 Cine SSFP
and LGE
CA mean proportion
of atrial enhancement
was significantly greater
compared to SH and NIDCM
Maurizio et
al.23 2015
77 LGE CMR Hypertrophied septum
indicating regional fibrosis
in HCM
Schwab et
al.24 2015
43 CMR Wall motion abnormalities
Nguyen et
al.25 2015
23 CMR/LGE
CMR
Diffuse myocardial fibrosis
Dungu et al.26
2013
97 LGE CMR Distinguished ATTR from AL
cardiac amyloidosis
Ferreira et
al.27 2013
50 T1 mapping
CMR
T1 mapping is a criterion
for detection of acute
myocarditis with a higher
sensitivity
Choi et al.28
2016
114 Cine CMR/
LGE CMR
Classification of distribution
of trabeculation, 43.9%
global type, 56.2% apical
type
Gulsin et al.29
2017
100 Cine CMR/
LGE CMR
Global LV hypokinesis

Abbreviations: CMR= cardiac magnetic resonance, LGE= late gadolinium enhancement, LE= late enhancement, CS= cardiac sarcoidosis, DCM= dilated cardiomyopathy, TIC= tachycardia induced cardiomyopathy, RVEDV= right ventricle end diastolic volume, RVEDS= right ventricle end systolic volume, CA= cardiac amyloidosis, SH= systemic hypertension, NIDCM= Nonischemic dilated cardiomyopathy, HCM= hypertrophic cardiomyopathy, AL= amyloid light chain, ATTR= transthyretin related Amyloidosis, SSFP= steady state free precision