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. Author manuscript; available in PMC: 2021 Apr 26.
Published in final edited form as: Nat Genet. 2020 Oct 26;52(11):1219–1226. doi: 10.1038/s41588-020-00710-0

Extended Data Table 3. Association among clinical characteristics and CH mutational characteristics.

Myeloid PD, genes mutated in myeloid neoplasms; non-myeloid, genes not linked to myeloid neoplasms; myeloid PD, variants known to be myeloid drivers or putative somatic driver mutations in myeloid neoplasms; myeloid non-PD, mutations within genes linked to myeloid neoplasms but that are not putative drivers; non-myeloid PD, mutations that are putative somatic driver mutations of cancer in genes not linked to myeloid neoplasms; non-myeloid non-PD, mutations within genes not linked to myeloid neoplasms that are not putative drivers of cancer. Associations were evaluated using multivariable logistic regression models to generate heterogeneity p-values. Sensitivity analyses restricted to individuals with only one mutation yielded similar results. Age expressed in decile.

Variable (reference) OR 95% CI p
Age - 1 1–1.1 0.0011
Ethnicity (white) Asian 1 0.94–1.2 0.42
Black 0.9 0.82–1 0.053
Other 0.93 0.83–1 0.24
Unknown 0.92 0.8–1.1 0.22
Smoke (non-smoker) Smoker 1.1 1.1–1.2 0.000023
Therapy (untreated) Treated 1 0.96–1.1 0.8
PD status (non-PD non-myeloid) Myeloid PD 1.3 1.3–1.4 < 1 × 10−6
Non-myeloid PD 1.3 1.2–1.5 0.000052
Non-PD myeloid 0.99 0.92–1.1 0.8
Number of mutations (1) ≥ 2 1.1 1.1–1.2 0.0000038