Table 1.
Characteristic | Myeloid neoplasm development | Overall (N = 46,237) | P | |
---|---|---|---|---|
Yes (N = 115) | No (N = 46,122) | |||
Age, mean (SD; y) | 60.79 (7.5) | 57.31 (8.2) | 57.32 (8.2) | 2.1E−06 |
Sex, female | 48 (41.7%) | 24,770 (53.7%) | 24,818 (53.7%) | 0.01 |
Race | 0.82 | |||
White | 110 (95.7%) | 42,973 (93.2%) | 43,083 (93.2%) | |
Black | 2 (1.7%) | 1,068 (2.3%) | 1,070 (2.3%) | |
Asian | 2 (1.7%) | 1,016 (2.2%) | 1,018 (2.2%) | |
Other | 1 (0.9%) | 836 (1.8%) | 837 (1.8%) | |
Missing | 0 (0%) | 229 (0.5%) | 229 (0.5%) | |
Smoking status | 4.7E−03 | |||
Never | 47 (40.9%) | 24,968 (54.1%) | 25,015 (54.1%) | |
Current or former | 68 (59.1%) | 20,936 (45.4%) | 21,004 (45.4%) | |
Missing | 0 (0%) | 218 (0.5%) | 218 (0.5%) | |
Blood counts, mean (SD) | ||||
Neutrophil count, ×109 cells/L | 4.42 (2.1) | 4.24 (1.4) | 4.24 (1.4) | 0.38 |
Lymphocyte count, ×109 cells/L | 1.90 (0.7) | 1.95 (0.7) | 1.95 (0.7) | 0.44 |
Monocyte count, ×109 cells/L | 0.59 (0.6) | 0.48 (0.2) | 0.48 (0.2) | 0.04 |
Eosinophil count, ×109 cells/L | 0.17 (0.1) | 0.17 (0.1) | 0.17 (0.1) | 0.75 |
Basophil count, ×109 cells/L | 0.04 (0.1) | 0.03 (0.0) | 0.03 (0.0) | 0.65 |
Hemoglobin concentration, g/dL | 13.9 (1.4) | 14.2 (1.3) | 14.2 (1.3) | 0.05 |
Mean corpuscular volume, fL | 92.4 (7.4) | 91.1 (4.6) | 91.1 (4.6) | 0.06 |
RBC distribution width (%) | 14.3 (1.8) | 13.5 (1.0) | 13.5 (1.0) | 5.0E−06 |
Platelet count, ×109 cells/L | 299 (126) | 252 (59) | 252 (59) | 1.7E−04 |
Clonal hematopoiesis (CH) | ||||
Detectable | 49.6% | 8.60% | 8.7% | |
CH-heme (SNV/indel) | 49 (42.6%) | 2,757 (6.0%) | 2,806 (6.1%) | 2.6E−29 |
0 variants | 66 (57.4%) | 43,365 (94.0%) | 43,431 (93.9%) | 1.6E−126 |
1 variant | 32 (27.8%) | 2,538 (5.5%) | 2,570 (5.6%) | |
≥2 variants | 17 (14.8%) | 219 (0.5%) | 236 (0.5%) | |
Mean VAF, mean (SD) | 0.26 (0.1) | 0.15 (0.1) | 0.15 (0.1) | 6.0E−08 |
CH-mCA | 23 (20.0%) | 1,369 (3.0%) | 1,392 (3.0%) | 5.5E−13 |
Note: Unless noted otherwise, data are n (%).
Abbreviations: SD, standard deviation; SNV, single-nucleotide variant; VAF, variant allele frequency; mCA, mosaic chromosomal alteration.