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In a nutshell
- While intermittent fasting improved health in older mice, it harmed pancreatic cell development in young mice, suggesting this popular diet trend may be risky for adolescents and young adults
- Short-term fasting (5 weeks) was safe for all age groups, but long-term fasting (10 weeks) caused problems with insulin production in young subjects that resembled early-stage Type 1 diabetes
- The research challenges the one-size-fits-all approach to intermittent fasting, indicating that age should be a key factor when considering this eating pattern
MUNICH — Intermittent fasting has become one of the most popular eating patterns of the past decade. The practice, which involves cycling between periods of eating and fasting, has been praised for its potential health benefits. But a new mouse model study suggests that age plays a crucial role in how the body responds to fasting — and for young individuals, it might do more harm than good.
A team of German researchers recently discovered that while intermittent fasting improved health markers in older mice, it actually impaired important cellular development in younger ones. Their findings, published in Cell Reports, raise important questions about who should (and shouldn’t) try this trending eating pattern.
Inside our bodies, specialized cells in the pancreas produce insulin, a hormone that helps control blood sugar levels. These cells, called beta cells, are particularly important during youth when the body is still developing. The researchers found that in young mice, long-term intermittent fasting disrupted how these cells grew and functioned.
โOur study confirms that intermittent fasting is beneficial for adults, but it might come with risks for children and teenagers,โ says Stephan Herzig, a professor at Technical University of Munich and director of the Institute for Diabetes and Cancer at Helmholtz Munich, in a statement.
The study looked at three groups of mice: young (equivalent to adolescence in humans), middle-aged (adult), and elderly. Each group followed an eating pattern where they fasted for 24 hours, followed by 48 hours of normal eating. The researchers tracked how this affected their bodies over both short periods (5 weeks) and longer periods (10 weeks).
At first, all age groups showed improvements in how their bodies handled sugar, which, of course, is a positive sign. But after extended periods of intermittent fasting, significant differences emerged between age groups. While older and middle-aged mice continued to show benefits, the young mice began showing troubling changes.
The pancreatic cells in young mice became less effective at producing insulin, and they weren’t maturing properly. Even more concerning, these cellular changes resembled patterns typically seen in Type 1 diabetes, a condition that usually develops in childhood or adolescence.
โIntermittent fasting is usually thought to benefit beta cells, so we were surprised to find that young mice produced less insulin after the extended fasting,โ explains co-lead author Leonardo Matta, from Helmholtz Munich.
The older mice, however, actually benefited from the extended fasting periods. Their insulin-producing cells worked better, and they showed improved blood sugar control. Middle-aged mice maintained stable function, suggesting that mature bodies handle fasting periods differently than developing ones.
This age-dependent response challenges the common belief that intermittent fasting is suitable for everyone. The research suggests that while mature adults might benefit from this eating pattern, young people could be putting themselves at risk, particularly if they maintain the practice for extended periods.
The findings are especially relevant given how popular intermittent fasting has become among young people looking to manage their weight. While short-term fasting appeared safe across all age groups, the long-term effects on young practitioners could be significant.
โThe next step is digging deeper into the molecular mechanisms underlying these observations,” says Herzig. “If we better understand how to promote healthy beta cell development, it will open new avenues for treating diabetes by restoring insulin production.โ
Despite the attention they receive from athletes and wellness influencers, popular dietary trends aren’t one-size-fits-all. What works for adults might not be appropriate for growing bodies — all the more reason that understanding these age-related differences becomes increasingly important.
Paper Summary
Methodology
The researchers studied male mice of different ages, having them alternate between one day of fasting and two days of normal eating. They monitored blood sugar levels, insulin production, and examined pancreatic tissue samples. They also used advanced technology to study genetic changes in individual cells.
Results
Brief periods of fasting (5 weeks) improved blood sugar control in all age groups. However, extended fasting (10 weeks) affected age groups differently: older mice showed better cellular function, middle-aged mice stayed stable, but young mice experienced problems with cell development and hormone production.
Limitations
The research only looked at male mice, so we don’t know if females would respond differently. While mice are often used to study human biology, people might react differently to fasting. Also, the age groups studied in mice don’t perfectly match human age groups.
Key Takeaways
The timing of intermittent fasting in life matters significantly. While it might benefit or maintain health in adults and older individuals, it could potentially harm developing bodies. The research suggests we need different dietary recommendations for different age groups.
Funding and Disclosures
This study was funded by several European research institutions and grant programs. The researchers declared no conflicts of interest.
Publication Details
The study appeared in Cell Reports on February 25, 2025, authored by Leonardo Matta and colleagues from various German research centers. The full paper, “Chronic intermittent fasting impairs ฮฒ cell maturation and function in adolescent mice,” is freely available to the public.