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Determination of Left Ventricular Mass on Cardiac Computed Tomographic Angiography1

Rationale and Objectives

Left ventricular hypertrophy (LVH) is associated with an increased risk of cardiac death. The present study evaluates whether using computed tomographic (CT)–derived criteria for normal myocardial mass can improve detection of LVH on CT angiography (CTA).

Materials and Methods

A total of 2238 subjects (63 ± 9 years, 27% female) who underwent CTA were studied. To identify normal limits for CT-derived myocardial mass, we studied normal subjects (those without diabetes, hypertension, congestive heart failure, or coronary artery disease). Left ventricular mass (LVM) was measured manually using two different workstations. The CT criteria of LVH was defined as LVM above the 97th percentile per gender and compared to echocardiographic criteria (110 g/m 2 in women; 124 g/m 2 in men), and specificity and sensitivity of both models to detect LVH were calculated.

Results

The LVM was higher in men than women in normal cohorts (75.5 ± 14.0 vs. 63.1 ± 12.8 g/m 2 , P = .001 with electron beam CTA and 78.5 ± 11.9 vs. 65.0 ± 9.2 g/m 2 , P = .001 with 64 multidetector [MD] CT, respectively). The coefficient of variation between electron beam CTA and 64 MDCT for measuring LVM was 3.1%. Comparing the new CTA/64 MDCT criteria of LVH (103.0 g/m 2 in men; 89.0 g/m 2 in women) to the previous echocardiographic criteria of LVH, the specificity in women and men decreased from 100% in both genders by echocardiography to 91.8% and 92.6%, respectively, but the sensitivity increased from 42.0% to 100% and from 41.1% to 100%.

Conclusion

This study suggests that CT-measured LVM has low variability and normal values based on CT criteria will potentially increase the early detection of LVH.

Left ventricular hypertrophy (LVH) is the earliest manifestation of cardiac damage in hypertension , and is an independent predictor of cardiovascular events . The detection and quantification of LVH is an important target to monitor the efficacy of antihypertensive therapies . Two-dimensional echocardiography has been used to measure left ventricular mass (LVM) for the past two decades , but because of significant improvement in measuring techniques, other modalities, including magnetic resonance imaging (MRI) , computed tomography (CT) , multiple detector row CT (MDCT) , and three-dimensional echocardiography have been accepted as alternatives for accurate LVH measurement. Electron beam (EB) computed tomographic angiographic (CTA) and 64 MDCT with high spatial resolution can accurately differentiate the endocardial and epicardial boundaries and provide detailed information of cardiac structures that should allow for precise measurement of the chamber volume and LVM without assumptions regarding geometry . Studies have used various criteria to measure LVH with different imaging modalities , but previous CT-defined criteria are still challenging and have a very low sensitivity to detect LVH . The present study evaluates whether a new criteria for LVH on CTA/MDCT can improve detection of LVH.

Methods

Study Population

We enrolled consecutive patients without known causes of increased LVM to define the normal and 97th percentiles for both men and women from among 2238 consecutive subjects (mean 63 ± 9 years, 27% women) who underwent CTA with EB and 458 subjects who underwent 64 MDCT. Excluded were those patients with known coronary artery disease, congestive heart failure or ejection fraction <50%, hypertension, or diabetes. The study protocol was approved by the Los Angeles Biomedical Research Institute at Harbor UCLA Medical Center, Torrance, CA.

EBCT Angiographic Study

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MDCT Study Protocol

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Measurement of LVM with CTA and 64 MDCT

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Figure 1, Left ventricular (LV) mass measurement at end-systolic phase. Right superior and left inferior panels are LV base and apex without cavity; left superior and right inferior panels are LV mid slice levels. The red and blue lines represent traced endocardial and epicardial boundaries, respectively. The papillary muscle was excluded from measures. The LV cavity volume, total LV volume (myocardial + cavity) was measured. LV mass (G) was calculated by this formula: 1.05 g/mL × (total LVV − LV cavity volume). The slice thickness is 1.5 or 3 mm. A total of 6–10 slices need be traced in each study. The other slices that were not manually traced are automatically completed by computer. LA, left atrium; LV, left ventricle; RA, right atrium; RV, right ventricle.

Table 1

Relationship between Left Ventricular Mass and Gender

Gender No. Age (y) Weight (lb) Height (in) BSA LVEF (%) LVM (G) Group 1A Female 247 60 67.3 162.1 1.72 69.4 63.1 (CTA) Male 551 58 82.5 176.5 1.99 68.3 75.5 Group 1B Female 166 61.7 159.0 63.4 1.75 66.1 65.0 (MDCT) Male 292 59.6 193.3 69.9 2.05 64.3 78.5 Group 2 Female 146 63 73.2 162.3 1.78 70.9 63.2 Male 283 63 87.4 176.0 2.04 69.1 75.3

BSA, body surface area; CTA, computed tomographic angiography; LVEF, left ventricular ejection fraction; LVM, left ventricular mass; MDCT, multiple detector row computed tomography.

Group 1A and 1B: normal; Group 2: hypertension with normal LVEF.

∗ Significant difference with normal group ( P < .001).

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Left Ventricular Ejection Fraction Measurement with Cine Image of CTA and 64 MDCT

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Figure 2, Left ventricular ejection fraction (LVEF) measurement; right and left panels represent diastolic and systolic, respectively. The upper, middle, and lower panels are LV base, mid, and apical slice levels. The LV cavity volume at end systolic (LVVes) is calculated as the volume within the red line multiplied by the slice thickness. The total LV volume at end-diastolic and end-systolic (TLVVed and TLVVes = mass + cavity) phases were calculated as within the blue line , multiplied by the slice thickness. LV stroke volume (LVSV) = T LVVed − TLVVes, LVEF = LVSV/ (LVVes + LVSV) × 100%. LA, left atrium; LV, left ventricle; LVC, LV cavity volume; RA, right atrium; RV, right ventricle.

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Variability of LVM Measurement

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Table 2

Variability of Left Ventricular Mass Measurement

Variability No.R V CV Bland Altman plot ratio Interobserver 21 0.96 ∗ 6.1 3.7 0.99 (95%CI: 0.97–1.01) Interscan 27 0.96 ∗ 5.5 3.8 1.0 (95%CI: 0.98–1.03) Different phases (ES and ED) 71 0.98 ∗ 6.2 3.7 0.97 (95%CI: 0.95–0.98) Inter AW and Terarecon 865 0.93 ∗ 7.7 4.5 1.01 (95%CI: 0.99–1.02) Inter EBA and CTA 30 0.81 4.9 3.1 0.96 (95% CI: 0.93–0.97)

CV, coefficient of variation by Bland-Altman model; EBA, electron beam angiogram; ED, end diastolic; ES, end systolic; R , R value; V, variation between two measurements.

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Statistical Analyses

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Results

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Table 3

Sensitivity and Specificity of New Criteria to Detect Left Ventricular Hypertrophy as Compared to the Previous Criteria

Group Left Ventricular Mass Women Men No. ≥110 g/m 2 <110 g/m 2 ≥89 g/m 2 <89 g/m 2 No. ≥124 g/m 2 <124 g/m 2 ≥103 g/m 2 <103 g/m 2 Group 1A 247 1 246 7 240 551 0 551 17 534 Group 1B 166 0 166 4 164 292 0 292 6 286 Group 2 146 3 243 9 137 283 7 276 19 264 617 Sen Spec Sen Spec 1621 Sen Spec Sen Spec (%) (%) (%) (%) (%) (%) (%) (%) LVH 42.0 100 100 91.8 41.1 100 100 92.6

LVH, left ventricular hypertrophy diagnosed by computed tomographic angiography; Sen, sensitivity; spec, specificity.

Group 1A and 1B: normal; Group 2: hypertension with normal left ventricular ejection fraction.

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Discussion

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Standard Cut Point for LVH

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Table 4

Criteria of Left Ventricular Hypertrophy (2 SD above Mean LVM or 97th Percentile of LVM) with Different Imaging Modalities

Author No. LVM (g/m 2 ) Image Female Male Mao 798 89 103 EBT Verdecchia 1064 110 124 M-D Echo Devereux 94 110 134 M-D Echo Hees 336 115 135 MRI Lorenz 75 95 113 MRI Alfakin 60 77 96 MRI-TGE Alfakin 60 67 83 MRI-SSFP Rumberger – 134 134 EBT Lang – 95 115 Echo

EBT, electron beam computed tomography; echo, echocardiogram; LVM, left ventricular mass; MRI, magnetic resonance imaging; SSFP, steady-state free precession; TGE, turbo gradient echo.

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Variability of LVM Measurement

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Comparison among EBT, MRI, Three-dimensional Echocardiography, and MDCT

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Limitations

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Conclusion

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