PMID- 22510429 OWN - NLM STAT- MEDLINE DCOM- 20121113 LR - 20211021 IS - 1474-9726 (Electronic) IS - 1474-9718 (Print) IS - 1474-9718 (Linking) VI - 11 IP - 4 DP - 2012 Aug TI - Caloric restriction may reverse age-related autonomic decline in humans. PG - 644-50 LID - 10.1111/j.1474-9726.2012.00825.x [doi] AB - Caloric restriction (CR) retards aging in laboratory rodents. No information is available on the effects of long-term CR on physiologic markers of aging and longevity in humans. Heart rate variability (HRV) is a marker for cardiac autonomic functioning. The progressive decline in HRV with aging and the association of higher HRV with better health outcomes are well established. Heart rate variability assessment is a reliable tool by which the effects of CR on autonomic function can be assessed. Time- and frequency-domain analyses compared 24-h HRV in 22 CR individuals aged 35-82 years and 20 age-matched controls eating Western diets (WD). The CR group was significantly leaner than the WD group. Heart rate was significantly lower, and virtually, all HRV values were significantly higher in the CR group than in the WD group (P < 0.002). Heart rate variability in the CR individuals was comparable with published norms for healthy individuals 20 years younger. In addition, when differences in heart rate (HR) and HRV between CR and WD were compared with previously published changes in HRV induced in healthy adults given atenolol, percent differences in each measure were generally similar in direction and magnitude and suggested declines in sympathetic and increases in parasympathetic modulation of HR and increased circadian variability associated with CR. These findings provide evidence that CR has direct systemic effects that counter the expected age-associated changes in autonomic function so that HRV indexes in CR individuals are similar to those of individuals 20 years younger eating WDs. CI - (c) 2012 The Authors. Aging Cell (c) 2012 Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland. FAU - Stein, Phyllis K AU - Stein PK AD - HRV Laboratory, Washington University School of Medicine, St. Louis, MO 63110, USA. pstein@dom.wustl.edu FAU - Soare, Andreea AU - Soare A FAU - Meyer, Timothy E AU - Meyer TE FAU - Cangemi, Roberto AU - Cangemi R FAU - Holloszy, John O AU - Holloszy JO FAU - Fontana, Luigi AU - Fontana L LA - eng GR - P30 DK056341/DK/NIDDK NIH HHS/United States GR - UL1 RR024992/RR/NCRR NIH HHS/United States GR - UL1 TR000448/TR/NCATS NIH HHS/United States GR - P30DK056341/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20120521 PL - England TA - Aging Cell JT - Aging cell JID - 101130839 SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Aging/*physiology MH - Analysis of Variance MH - Autonomic Nervous System/*physiology MH - *Caloric Restriction MH - Case-Control Studies MH - Female MH - Heart Rate/physiology MH - Humans MH - Longevity/physiology MH - Male MH - Middle Aged MH - Risk Factors PMC - PMC3598611 MID - NIHMS373745 EDAT- 2012/04/19 06:00 MHDA- 2012/11/14 06:00 PMCR- 2013/08/01 CRDT- 2012/04/19 06:00 PHST- 2012/04/19 06:00 [entrez] PHST- 2012/04/19 06:00 [pubmed] PHST- 2012/11/14 06:00 [medline] PHST- 2013/08/01 00:00 [pmc-release] AID - 10.1111/j.1474-9726.2012.00825.x [doi] PST - ppublish SO - Aging Cell. 2012 Aug;11(4):644-50. doi: 10.1111/j.1474-9726.2012.00825.x. Epub 2012 May 21.