Table 2.

Epigenetic clock values, residuals, and associations with various clinical characteristics

Median (SD)Welch t test–P valueLinear regressions–P valuePearson’s correlation coefficient - r (P value)
Biological sexSCD genotypeβ-globin haplotypeSCD disease severityBCL11A SNPChronological ageGenetic ancestry
DNAmAge (Horvath) age 0.40 (4.48) .89 .61 .28 .93 .99 .88 (<1e-5)∗∗ .212 (.057) 
DNAmAge (Hannum) age −3.98 (3.86) .62 .11 .89 .92 .71 .89 (<1e-5)∗∗ .173 (.120) 
PhenoAge age −8.65 (6.00) .23 .02∗ .34 .90 .26 .85 (<1e-5)∗∗ .092 (.411) 
GrimAge age 11.90 (4.02) .96 .19 .52 .67 .69 .88 (<1e-5∗)∗∗ .176 (.114) 
DunedinPACE rate 1.14 (0.12) .07 <.001∗∗ .41 .56 .79 .34 (.001)∗∗ .041 (.722) 
DNAmAge (Horvath) residuals 0.07 (4.50) .25 .61 .29 .83 .54 NA .181 (.104) 
DNAmAge (Hannum) residuals 0.24 (3.78) .96 .07 .30 .54 .87 NA −.001 (.994) 
PhenoAge residuals 0.08 (5.89) .10 .03∗ .39 .59 .11 NA −.135 (.226) 
GrimAge residuals −0.30 (3.94) .25 .10 .96 .95 .81 NA .015 (.894) 
Median (SD)Welch t test–P valueLinear regressions–P valuePearson’s correlation coefficient - r (P value)
Biological sexSCD genotypeβ-globin haplotypeSCD disease severityBCL11A SNPChronological ageGenetic ancestry
DNAmAge (Horvath) age 0.40 (4.48) .89 .61 .28 .93 .99 .88 (<1e-5)∗∗ .212 (.057) 
DNAmAge (Hannum) age −3.98 (3.86) .62 .11 .89 .92 .71 .89 (<1e-5)∗∗ .173 (.120) 
PhenoAge age −8.65 (6.00) .23 .02∗ .34 .90 .26 .85 (<1e-5)∗∗ .092 (.411) 
GrimAge age 11.90 (4.02) .96 .19 .52 .67 .69 .88 (<1e-5∗)∗∗ .176 (.114) 
DunedinPACE rate 1.14 (0.12) .07 <.001∗∗ .41 .56 .79 .34 (.001)∗∗ .041 (.722) 
DNAmAge (Horvath) residuals 0.07 (4.50) .25 .61 .29 .83 .54 NA .181 (.104) 
DNAmAge (Hannum) residuals 0.24 (3.78) .96 .07 .30 .54 .87 NA −.001 (.994) 
PhenoAge residuals 0.08 (5.89) .10 .03∗ .39 .59 .11 NA −.135 (.226) 
GrimAge residuals −0.30 (3.94) .25 .10 .96 .95 .81 NA .015 (.894) 

Associations between sex and sickle cell genotype (dichotomous continuous variables) were calculated using the Welch t tests. Associations with SCD severity, β-globin haplotype, and BCL11A SNP (polytomous ordinal variables) were calculated using linear regression. Associations between chronological age and genetic ancestry (continuous variables) were calculated using Pearson correlation coefficient. ∗P < 0.05; ∗∗P < 0.001.

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