Kleckner Amber S, Clingan Carin L, Youngblood Shari M, Kleckner Ian R, Quick Lauren, Elrod Rebecca D, Zhu Shijun, Manoogian Emily N C, Panda Satchidananda, Badros Ashraf Z, Emadi Ashkan
University of Maryland School of Nursing.
The Salk Institute for Biological Sciences.
Res Sq. 2024 Dec 25:rs.3.rs-5530166. doi: 10.21203/rs.3.rs-5530166/v1.
Time-restricted eating (TRE) helps regulate rest-activity rhythms, blood glucose, and other diurnally regulated energetics processes, which may have implications for persistent fatigue. In a randomized controlled trial, we tested the effects of TRE vs. control on fatigue in cancer survivorship.
Adult cancer survivors were recruited who were 2 months to 2 years post-treatment and reported moderate to severe fatigue. Participants were randomized 1:1, TRE:control and all received individualized nutrition counseling. The TRE group self-selected a 10-hour eating window for 12 weeks. At baseline, week 6, and week 12, participants were asked to log eating instances, complete the Functional Assessment of Chronic Illness Therapy-Fatigue questionnaire (FACIT-F, higher score=less fatigue), and wear an actigraph and continuous glucose monitor.
Thirty participants completed baseline assessments and were randomized (77% female, 53% Black/African American, 43% White, 7% Hispanic; 54.1±14.7 years old; 87% with blood cancer); 25 completed 12-week assessments. TRE led to a meaningful reduction in fatigue at week 12 controlling for baseline levels (change in FACIT-F fatigue subscale=0.0±5.4 for control, 4.1±5.7 for TRE, =0.11, effect size [ES]=0.70; clinically meaningful threshold=3.0 points). Glucose parameters (e.g., average interstitial glucose, average fasting glucose) tended to be lower and rest-activity rhythms tended to indicate more regularity for those in the TRE vs. control group at weeks 6 and 12, though differences were not statistically significant (>0.19).
A 12-week, nutritionist-led TRE program led to less fatigue than control. Continued study of TRE patterns are warranted to optimize this eating pattern and address persistent cancer-related fatigue.
限时进食(TRE)有助于调节休息-活动节律、血糖及其他昼夜调节的能量代谢过程,这可能对持续性疲劳有影响。在一项随机对照试验中,我们测试了限时进食与对照饮食对癌症幸存者疲劳的影响。
招募治疗后2个月至2年且报告有中度至重度疲劳的成年癌症幸存者。参与者按1:1随机分组,即限时进食组:对照组,两组均接受个性化营养咨询。限时进食组自行选择10小时的进食窗口,为期12周。在基线、第6周和第12周时,要求参与者记录进食情况,完成慢性病治疗功能评估-疲劳问卷(FACIT-F,得分越高表示疲劳越少),并佩戴活动记录仪和持续血糖监测仪。
30名参与者完成了基线评估并被随机分组(77%为女性,53%为黑人/非裔美国人,43%为白人,7%为西班牙裔;年龄54.1±14.7岁;87%为血癌患者);25名完成了12周评估。在控制基线水平的情况下,限时进食在第12周时使疲劳有显著减轻(FACIT-F疲劳子量表变化:对照组为0.0±5.4,限时进食组为4.1±5.7,P=0.11,效应量[ES]=0.70;临床意义阈值为3.0分)。在第6周和第12周时,限时进食组的血糖参数(如平均组织间液葡萄糖、平均空腹血糖)往往较低,休息-活动节律往往更规律,尽管差异无统计学意义(P>0.19)。
由营养师指导的为期12周的限时进食计划比对照组导致的疲劳更少。有必要继续研究限时进食模式,以优化这种饮食模式并解决持续性癌症相关疲劳问题。