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The augmentation pressure and AIx both increased with aging.
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After adjustment for sex, F&V intake and dietary costs both increased with age.
SBP and DBP both increased with age (p < 0.001).
As a result, modelled harms and benefits both increased with age but the benefits increased faster.
Ery-Cd and U-Cd were positively correlated, and both increased with age (Table 2).
Onset and persistence both increased with age, and were most frequently recorded for restricted mobility outside the home.
Autoantibodies to M3R were observed in both strains and significantly increased with aging in both strains.
We also showed that M3R autoantibodies increased with aging in both γDKO and CD25KO strains.
M3R autoantibodies increased with aging in both the γDKO and the CD25KO strains.
Sero-positivity to both antigens increased with age and was higher in the Korogwe health facilities (MSP-119 and AMA-1 both p<0.001; Table 2).
Among patients younger than 70, the rate of amputation for both cohorts increased with age.
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