Decreased Energy Availability During Training Overload Is Associated With Non-Functional Overreaching And Suppressed Ovarian Function In Female Runners

Low energy availability (EA) suppresses many physiological processes, including ovarian function in female athletes. Low EA could also predispose athletes to develop a state of overreaching. This study compared the changes in ad libitum energy intake (EI), exercise energy expenditure (ExEE), and EA among runners completing a training overload (TO) phase. We tested the hypothesis that runners becoming overreached would show decreased EA, suppressed ovarian function and plasma leptin, compared with well-adapted (WA) runners. After 1 menstrual cycle (baseline),16 eumenorrheic runners performed 4 weeks of TO followed by a 2-week recovery (131 +/- 3% and 63 +/- 6% of baseline running volume, respectively). Seven-day ExEE, EI, running performance (RUNperf) and plasma leptin concentration were assessed for each phase. Salivary estradiol concentration was measured daily. Urinary luteinizing hormone concentration tests confirmed ovulation. Nine runners adapted positively to TO (WA, Delta RUNperf: +4 +/- 2%); 7 were non-functionally overreached (NFOR; Delta RUNperf: -9 +/- 2%) as RUNperf remained suppressed after the recovery period. WA increased El during TO, maintaining their baseline EA despite a large increase in ExEE (Delta EA = +1.9 +/- 1.3 kcal.kg fat free mass (FFM)(-1).d(-1), P = 0.17). By contrast, NFOR showed no change in EI, leading to decreased EA (Delta EA = 5.6 +/- 2.1 kcal.kg FFM-1.d(-1), P = 0.04). Plasma leptin concentration mid-cycle and luteal salivary estradiol concentration decreased in NFOR only. Contrasting with WA, NFOR failed to maintain baseline EA during TO, resulting in poor performance outcomes and suppressed ovarian function.Novelty:Runners adapting positively to training overload (TO) increased ad libitum energy intake, maintaining baseline EA and ovarian function through TO.By contrast, NFOR runners failed to increase energy intake, showing suppressed EA and ovarian function during TO.