Age acceleration needs a clock-specific reference
For the reported association between clonal haematopoiesis and epigenetic age acceleration, the key calibration is distance from the expected methylation-age distribution, not merely a positive acceleration label. Are estimates reported separately by clock, chronological age range, blood-cell composition, and reference population? Agreement across those contexts would support a broad shift, whereas divergence could indicate a partial pattern concentrated in particular CpGs or cell fractions.
