Table 2 No effect of subclinical atherosclerosis on the expansion of mutant hematopoietic clones

From: Unidirectional association of clonal hematopoiesis with atherosclerosis development

 

AER

log (VAF ratio)/time

Exponential growth rate

Estimate

Standard error

P value

Estimate

Standard error

P value

Estimate

Standard error

P value

Baseline presence of atherosclerosis

 CACS >0

−1.907

1.474

0.196

−1.161

0.893

0.194

−1.266

0.94

0.179

 Global plaque volume >0

0.718

1.183

0.544

0.034

0.734

0.963

0.075

0.772

0.923

 Carotid plaque volume >0

0.526

1.321

0.691

−0.071

0.798

0.929

−0.016

0.841

0.985

 Femoral plaque volume >0

1.012

1.287

0.432

0.155

0.803

0.847

0.205

0.843

0.808

Baseline extent of atherosclerosis

 CACS (Agatston)

0.003

0.005

0.524

0.003

0.003

0.376

0.003

0.003

0.392

 Global plaque volume (mm3)

−0.007

0.007

0.304

-0.005

0.004

0.2

−0.005

0.004

0.214

 Carotid plaque volume (mm3)

−0.019

0.025

0.46

−0.005

0.014

0.742

−0.006

0.015

0.695

 Femoral plaque volume (mm3)

−0.013

0.008

0.127

-0.009

0.005

0.061

−0.009

0.005

0.069

Cumulative atherosclerosis burden over 6years

 CACS (AUC)

1.816

10.08

0.857

3.044

6.121

0.619

2.867

6.444

0.657

 Global plaque volume (AUC)

−7.095

6.955

0.308

−4.934

4.305

0.252

−5.38

4.53

0.236

 Carotid plaque volume (AUC)

−9.817

14.13

0.488

−4.569

8.526

0.592

−5.268

8.99

0.558

 Femoral plaque volume (AUC)

−11.047

8.223

0.18

−9.13

5.111

0.075

−9.53

5.371

0.077

  1. We monitored the expansion of 602 CH-related mutations through serial sequencing of blood samples from 494 individuals at baseline and 6 years after enrollment. We then investigated the association between baseline or cumulative atherosclerosis burden and different metrics of clonal expansion rates through mixed-effects models. The presence of subclinical atherosclerosis at baseline was defined as a categorical variable on the basis of CACS or 3DVUS imaging. The extent of subclinical atherosclerosis at baseline in those with detectable atherosclerosis in specific regions was defined as a continuous variable on the basis of CACS or 3DVUS imaging. The cumulative burden of subclinical atherosclerosis over the timeframe of this longitudinal analysis was estimated as the AUC for CACS and atherosclerotic plaque volumes, assessed by CT and 3DVUS imaging, respectively, at three different time points over 6 years.