TY - JOUR
T1 - ENabling Reduction of Low-grade Inflammation in SEniors Pilot Study
T2 - Concept, Rationale, and Design
AU - ENRGISE Pilot study investigators
AU - Manini, Todd M.
AU - Anton, Stephen D.
AU - Beavers, Daniel P.
AU - Cauley, Jane A.
AU - Espeland, Mark A.
AU - Fielding, Roger A.
AU - Kritchevsky, Stephen B.
AU - Leeuwenburgh, Christiaan
AU - Lewis, Kristina H.
AU - Liu, Christine
AU - McDermott, Mary M.
AU - Miller, Michael E.
AU - Tracy, Russell P.
AU - Walston, Jeremy D.
AU - Radziszewska, Barbara
AU - Lu, Jane
AU - Stowe, Cindy
AU - Wu, Samuel
AU - Newman, Anne B.
AU - Ambrosius, Walter T.
AU - Pahor, Marco
N1 - Funding Information:
Conflict of Interest: The ENRGISE Pilot Study is funded by National Institutes of Health (NIH), National Institute on Aging (NIA) Cooperative Agreement U01 AG050499 and sponsored in part by the Intramural Research Program, NIA, NIH. The research is partially supported by the Claude D. Pepper Older Americans Independence Centers at the University of Florida (1 P30 AG028740), Wake Forest University (1 P30 AG21332), Tufts University (1P30AG031679), and University of Pittsburgh (P30 AG024827). Dr. Roger Fielding (Tufts University) is partially supported by the U.S. Department of Agriculture under agreement 58–1950–0-014. The views of the authors do not reflect those of the Department of Agriculture. Abbott Laboratories provided funding for the purchase of the study drug and matching placebo.
Publisher Copyright:
© 2017, Copyright the Authors Journal compilation © 2017, The American Geriatrics Society
PY - 2017/9
Y1 - 2017/9
N2 - Objectives: To test two interventions to reduce interleukin (IL)-6 levels, an indicator of low-grade chronic inflammation and an independent risk factor for impaired mobility and slow walking speed in older adults. Design: The ENabling Reduction of low-Grade Inflammation in SEniors (ENRGISE) Pilot Study was a multicenter, double-blind, placebo-controlled randomized pilot trial of two interventions to reduce IL-6 levels. Setting: Five university-based research centers. Participants: Target enrollment was 300 men and women aged 70 and older with an average plasma IL-6 level between 2.5 and 30 pg/mL measured twice at least 1 week apart. Participants had low to moderate physical function, defined as self-reported difficulty walking one-quarter of a mile or climbing a flight of stairs and usual walk speed of less than 1 m/s on a 4-m usual-pace walk. Intervention: Participants were randomized to losartan, omega-3 fish oil (ω-3), combined losartan and ω-3, or placebo. Randomization was stratified depending on eligibility for each group. A titration schedule was implemented to reach a dose that was safe and effective for IL-6 reduction. Maximal doses were 100 mg/d for losartan and 2.8 g/d for ω-3. Measurements: IL-6, walking speed over 400 m, physical function (Short Physical Performance Battery), other inflammatory markers, safety, tolerability, frailty domains, and maximal leg strength were measured. Results: Results from the ENRGISE Pilot Study will provide recruitment yields, feasibility, medication tolerance and adherence, and preliminary data to help justify a sample size for a more definitive randomized trial. Conclusion: The ENRGISE Pilot Study will inform a larger subsequent trial that is expected to have important clinical and public health implications for the growing population of older adults with low-grade chronic inflammation and mobility limitations.
AB - Objectives: To test two interventions to reduce interleukin (IL)-6 levels, an indicator of low-grade chronic inflammation and an independent risk factor for impaired mobility and slow walking speed in older adults. Design: The ENabling Reduction of low-Grade Inflammation in SEniors (ENRGISE) Pilot Study was a multicenter, double-blind, placebo-controlled randomized pilot trial of two interventions to reduce IL-6 levels. Setting: Five university-based research centers. Participants: Target enrollment was 300 men and women aged 70 and older with an average plasma IL-6 level between 2.5 and 30 pg/mL measured twice at least 1 week apart. Participants had low to moderate physical function, defined as self-reported difficulty walking one-quarter of a mile or climbing a flight of stairs and usual walk speed of less than 1 m/s on a 4-m usual-pace walk. Intervention: Participants were randomized to losartan, omega-3 fish oil (ω-3), combined losartan and ω-3, or placebo. Randomization was stratified depending on eligibility for each group. A titration schedule was implemented to reach a dose that was safe and effective for IL-6 reduction. Maximal doses were 100 mg/d for losartan and 2.8 g/d for ω-3. Measurements: IL-6, walking speed over 400 m, physical function (Short Physical Performance Battery), other inflammatory markers, safety, tolerability, frailty domains, and maximal leg strength were measured. Results: Results from the ENRGISE Pilot Study will provide recruitment yields, feasibility, medication tolerance and adherence, and preliminary data to help justify a sample size for a more definitive randomized trial. Conclusion: The ENRGISE Pilot Study will inform a larger subsequent trial that is expected to have important clinical and public health implications for the growing population of older adults with low-grade chronic inflammation and mobility limitations.
KW - chronic inflammation
KW - immune system
KW - mobility disability
KW - physical function
UR - http://www.scopus.com/inward/record.url?scp=85029584372&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85029584372&partnerID=8YFLogxK
U2 - 10.1111/jgs.14965
DO - 10.1111/jgs.14965
M3 - Article
C2 - 28734043
AN - SCOPUS:85029584372
SN - 0002-8614
VL - 65
SP - 1961
EP - 1968
JO - Journal of the American Geriatrics Society
JF - Journal of the American Geriatrics Society
IS - 9
ER -