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Iron status determined changes in health measures induced by nordic walking with time-restricted eating in older adults– a randomised trial

  • Jakub Antoni Kortas,
  • Joanna Reczkowicz,
  • Ulana Juhas,
  • Ewa Ziemann,
  • Aleksandra Świątczak,
  • Katarzyna Prusik,
  • Szczepan Olszewski,
  • Nakisa Soltani,
  • Ewa Rodziewicz-Flis,
  • Damian Flis,
  • Małgorzata Żychowska,
  • Grażyna Gałęzowska,
  • Jędrzej Antosiewicz

摘要

Background and aims

This study evaluated whether stored iron determines the adaptive response induced by Nordic walking (NW) training combined with 10 hours’ time-restricted eating (TRE) in older adults.

Trial design and methods

Twenty-four participants underwent 12-week NW training supported by 10 h of TRE. The group was divided due to baseline ferritin concentration low < 75 ng/ml (LF) and high level ≥ 75 ng/ml (HF). Body composition, physical fitness and blood collection were assessed at baseline and post-intervention.

Results

NW + TRE induced a statistically significant decrease in ferritin levels in all participants (p = 0.01). Additionally, statistically significant intergroup differences in the LF vs. HF in the reduction of serum ferritin levels (p = 0.04) were observed. The procedure NW + TRE diminished HbA1c levels (p < 0.01) and glucose in all participants (p = 0.05). The range of HbA1c drop was more pronounced among those participants who experienced a greater decrease in the stored iron (p = 0.04, \( {\eta }_{p}^{2}\) =0.17, F=4.59). Greater changes in body weight and percent of body fat were recorded in the HF group (for both p<0.01).

Conclusion

Body iron stores determine the effects of a 12-week NW + TRE intervention on serum ferritin. The changes in HbA1c are more pronounced in subjects with a higher decrease in serum ferritin.

Trial registration

All experimental protocols were approved by the Bioethical Committee of the Regional Medical Society in Gdansk, Poland (NKBBN/330/2021) according to the Declaration of Helsinki. We confirm that all methods were carried out in accordance with relevant guidelines and regulations. The trial was registered as a clinical trial (NCT05229835, date of first registration: 14/01/2022, direct link: https://classic.clinicaltrials.gov/ct2/show/NCT05229835). Informed consent was obtained from all subjects.