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Table 3 Comparison of cardiac magnetic resonance imaging findings between the sarcomere gene and mitochondria-related gene mutation groups

From: Effect of sarcomere and mitochondria-related mutations on myocardial fibrosis in patients with hypertrophic cardiomyopathy

 

No pathogenic or likely pathogenic variant group (n = 67)

Only mitochondria-related nDNA or mtDNA variant groupa (n = 24)

Only sarcomere gene variant group (n = 36)

Sarcomere and mitochondria-related gene variant groupa (n = 5)

P

Late gadolinium enhancement (LGE)

     

Presence of LGE in left ventricle

42 (61)

12 (50)

32 (89)

5 nn

0.003

Number of LGE segments in left ventricle

2.9 ± 3.3

2.6 ± 3.8

5.0 ± 2.9**,††

4.2 ± 1.1

0.012

% LGE amount of left ventricle

6.4 ± 7.8

8.1 ± 13.0

10.9 ± 10.7*

8.3 ± 3.6

0.184

LGE in anteroseptal segments, %

20.9 ± 24.9

17.7 ± 28.1

47.2 ± 27.2**,††

40.0 ± 5.6

 < 0.001

LGE in septal segments, %

18.2 ± 24.8

15.0 ± 27.8

48.3 ± 31.5**,††

44.0 ± 16.7*,††

 < 0.001

LGE in inferoposterior segments, %

12.8 ± 23.8

15.0 ± 27.2

7.8 ± 14.6

8.0 ± 17.9

0.826

LGE in lateral segments, %

15.2 ± 25.4

11.7 ± 22.0

17.2 ± 20.9

12.0 ± 17.9

0.580

LGE in apical segments, %

28.4 ± 37.7

28.1 ± 35.6

37.5 ± 39.4

25.0 ± 25.0

0.643

Extracellular volume fraction (ECV), %

     

ECV average of 16 segments

31.5 ± 4.3

30.9 ± 4.5

34.0 ± 5.0*,†

35.4 ± 3.4

0.013

ECV in anteroseptal segments

31.9 ± 4.2

31.4 ± 5.0

35.6 ± 7.0**,††

36.9 ± 5.2*,†

0.002

ECV in septal segments

31.6 ± 3.9

30.7 ± 4.8

35.6 ± 6.9**,††

36.8 ± 5.8*,†

 < 0.001

ECV in inferoposterior segments

31.0 ± 4.6

30.2 ± 4.0

32.4 ± 4.1

34.8 ± 2.7

0.065

ECV in lateral segments

30.9 ± 5.2

30.0 ± 4.8

31.7 ± 4.1

32.4 ± 1.8

0.544

ECV in apical segments

33.7 ± 5.2

33.7 ± 6.4

35.3 ± 4.8

35.5 ± 4.3

0.500

  1. One patient was missed due to non-analysis of mtDNA
  2. aPathogenic or likely pathogenic mitochondria-related nDNA mutations or damaging mtDNA variants
  3. *P < 0.05
  4. **P < 0.01 versus no pathogenic or likely pathogenic variant group
  5. P < 0.05
  6. ††P < 0.01 versus mitochondria-related variant group