Once-weekly sirolimus 6 mg did not enhance short-term functional improvements from a home exercise program in older adults (mean difference -2.13 repetitions; 95% CI -4.61 to 0.34; p=0.089).
RCT (n=40)
Double-blind
1:1
Does once-weekly sirolimus enhance functional gains from a home-based exercise programme in sedentary older adults?
Once-weekly sirolimus did not enhance, and may have modestly attenuated, short-term functional improvements from a home exercise programme in older adults, while increasing adverse events.
Effect estimate: Mean difference -2.13 (95% CI -4.61 to 0.34)
p-value: p=0.089
ABSTRACT Background Preclinical models suggest alternating activation and inhibition of mechanistic target of rapamycin complex 1 (mTORC1) could enhance adaptation to exercise (‘cycling hypothesis’). Whether this concept translates to older adults is unknown. This exploratory trial assessed whether once‐weekly sirolimus (rapamycin) 6 mg enhances or inhibits functional gains from a home‐based exercise programme. Methods In this randomised, double‐blind, placebo‐controlled trial, 40 sedentary adults aged 65–85 years (mean 72.2 years; 47.5% female) were assigned (1:1) to sirolimus (rapamycin) 6 mg or matched placebo once weekly for 13 weeks. Both groups performed a standardised home‐based resistance (chair‐stands) and endurance (exercycle) programme three times/week. The primary outcome was the change in 30‐s chair‐stand repetitions at 13 weeks (intention‐to‐treat; ANCOVA adjusted for baseline performance, age stratum and sex). Complete‐case (CC) and per‐protocol (PP) analyses were prespecified sensitivity analyses. Secondary outcomes included grip strength, 6‐min walk distance, SF‐36 physical and mental component scores, C‐reactive protein and several epigenetic age measures. Safety was assessed through adverse‐event monitoring and laboratory tests. Results Both groups improved chair‐stand performance. The primary intention‐to‐treat analysis showed an adjusted mean difference (sirolimus–placebo) of −2.13 repetitions (95% CI −4.61 to 0.34; p = 0.089). Sensitivity analyses favoured placebo and reached statistical significance: complete‐case analysis (16 sirolimus, 19 placebo) showed a difference of −2.46 repetitions (95% CI −4.87 to −0.06; p = 0.045) and per‐protocol analysis (15 sirolimus, 16 placebo) showed −3.44 repetitions (95% CI −5.86 to −0.99; p = 0.007). Secondary functional outcomes also favoured placebo but were not statistically significant: the adjusted mean difference for 6MWD was −4.87 m (95% CI −28.97 to 19.71; p = 0.706) and for grip strength was −1.13 kg (95% CI −3.52 to 1.18; p = 0.344). SF‐36 scores showed small, non‐significant differences favouring placebo. Quality‐of‐life scores showed small, non‐significant differences favouring placebo. Seventeen participants (85%) in each arm reported ≥ 1 adverse event, but the total burden was higher with sirolimus (99 vs. 63 events), including one possibly drug‐related serious adverse event (pneumonia). Conclusion In this exploratory trial, once‐weekly sirolimus (rapamycin) 6 mg did not enhance, and in sensitivity analyses, it may have modestly attenuated short‐term functional improvements from a home exercise programme in older adults. The regimen also increased the burden of minor adverse events and may have contributed to one serious infection. Future trials with longer treatment duration or less frequent/lower dosing are needed to determine whether a favourable benefit–risk profile can be achieved. Trial Registration: ACTRN12624000790549
Stanfield et al. (2026) conducted an RCT in Sedentary older adults (n=40). Sirolimus (rapamycin) vs. Placebo was evaluated on Change in 30-s chair-stand repetitions at 13 weeks (Mean difference -2.13, 95% CI -4.61 to 0.34, p=0.089). Once-weekly sirolimus 6 mg did not enhance short-term functional improvements from a home exercise program in older adults (mean difference -2.13 repetitions; 95% CI -4.61 to 0.34; p=0.089).