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Volume 18 Supplement 1

19th Annual SCMR Scientific Sessions

  • Poster presentation
  • Open Access

T1 mapping across the ejection fraction spectrum

  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1,
  • 1 and
  • 1
Journal of Cardiovascular Magnetic Resonance201618 (Suppl 1) :P8

https://doi.org/10.1186/1532-429X-18-S1-P8

  • Published:

Keywords

  • Ejection Fraction
  • Short Axis Slice
  • Normal Ejection Fraction
  • Diffuse Fibrosis
  • Group Septal

Background

T1 mapping is a rapidly evolving field and is emerging as a novel quantitative tissue characterisation technique with potential applications in fibrosis, oedema, fat, iron and other patho-physiology. Its significance in heart failure is not yet fully explored but has the potential to add insights into disease processes and aid in refining diagnosis.

Methods

242 consecutive consenting patients referred for CMR between December 2014 and June 2015 were scanned on a 1.5T Magnetom Avanto (Siemens Healthcare, Erlangen) using a MOLLI (WIP#448, 5:3:3 acquisition scheme, motion correction and automatically generated T1 map). In all cases on the basal short axis slice, a single, slender ROI was placed in the mid wall of the septum with meticulous attention to avoid partial volume of blood/and or scar areas to derive the native T1 in msec. The patients were grouped by ejection fraction: <45%, 45-55% and >55%. 15 healthy volunteers were also used as a control group. Ejection fraction (EF), LV volumes, LV mass and BSA indexed left atrial area (LAAi) were also acquired. Comparison was performed using ANOVA and linear regression with adjustment for demographic variables that were found to vary between groups (age and BSAi LV mass).

Results

Baseline characteristics are given in the table. Unadjusted LAAi values were similar in the EF 44-55% and EF >55% groups (13.3 ± 3.5) but significantly higher in the EF <45% group (15.5 ± 4.6, p = 0.009), see figure 1. After adjustment for confounding variables, LAAi did not vary between groups (14.2, 13.8 and 13.6 respectively) p = 0.81. For septal T1, the adjusted and unadjusted analyses showed a significant difference between the 4 groups, with an inverse relationship between T1 value and EF as grouped in the study.

Figure 1

On pair wise comparisons between groups, there was no difference in T1 values between the <45% and 45-55% group in all analyses. The T1 difference between the 45-55% and >55% groups was significant only after adjusting for age, sex and LV mass p = 0.04. The control group septal T1 significantly varied from both the <45% and 45-55% groups (p => 0.001 and p = 0.03 respectively after adjusting for age and sex). There was no difference between the Septal T1 between the control group and the >55% group (p = 0.9 after adjusting for age and gender).

Conclusions

In a large cohort of consecutive patients, we have demonstrated that native T1 is prolonged in patients with low EF. Based on prior study, this is likely to reflect diffuse fibrosis. In addition we have shown that Native T1 is not different between patients referred for CMR with normal EF and healthy volunteers.

Table 1

Variable

EF <45% (n = 35) n (%)

EF 45-55% (n = 44) n (%)

EF >55% (n = 163) n (%)

Controls (n = 15) n (%)

P-value

Gender: Female

Male

14 (32%)

30 (68%)

10 (30%)

23 (70%)

74 (45%)

89 (55%)

9 (60%)

6 (40%)

0.09

 

Mean (SD)

Mean (SD)

Mean (SD)

Mean (SD)

 

Age

68.0 (10.3)

56.6 (17.6)

57.5 (17.7)

48.0 (13.4)

<0.001

BMI

27.1 (4.9)

27.9 (4.4)

28.1 (4.8)

-

0.50

BSA

1.95 (0.24)

1.99 (0.22)

1.95 (0.22)

-

0.70

LVmassi (g)

85.5 (23.5)

61.4 (13.3)

62.7 (17.8)

-

<0.001

Septal T1

1065(51)

1045(59)

1023(42)

1006+/-36

<0.001

Adjusted Septal T1

1066*

1047*

1023*

1005**

<0.001

 

Median (IQR)

Median (IQR)

Median (IQR)

  

End Diastolic Volume

197 (162, 248)

154 (130, 182)

132 (112, 159)

-

<0.001

*adjusted for age, gender and LVmassi. **adjusted for age and gender

Authors’ Affiliations

(1)
University Hospital Southampton NHS Foundation Trust, Southampton, UK

Copyright

© Alaour et al. 2016

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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