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Ozempic and Mounjaro linked to lower biological age in studies

Company research suggests semaglutide and tirzepatide may lower measures of biological age, but the findings do not establish that treatment extends life.

Eleanor WhitcombeEleanor WhitcombeHealth Editor3 min read
A laboratory researcher handling blood samples, reflecting work on Ozempic and measures of biological ageing
A laboratory researcher handling blood samples, reflecting work on Ozempic and measures of biological ageing

What Novo Nordisk and Eli Lilly reported on biological ageing

Eli Lilly and Novo Nordisk have presented research at the Aging Research & Drug Discovery conference suggesting that their weight-loss medicines may lower estimates of biological age by around two to three years. The findings concerned people with excess weight or diabetes, according to a New York Post report published on 11 October 2026.

The research involved semaglutide, sold as Ozempic and Wegovy, and tirzepatide, sold as Mounjaro. The companies used different laboratory methods to assess ageing, rather than measuring whether participants lived longer.

Novo Nordisk examined blood samples from 10,052 people, with half receiving semaglutide and half a placebo. Samples were taken at the beginning of the study and again months later, allowing researchers to examine changes in blood proteins over time.

Eli Lilly conducted a smaller study of tirzepatide using measurements based on DNA-related changes. The newspaper did not give the number of participants in that study.

The size of the apparent age reduction depended on the measurement used and the organ being assessed. One clock based on heart-related proteins suggested a difference of as much as four years. That was a result from a particular measure, not a finding that every participant’s body had become four years younger.

How biological clocks assess Ozempic and Mounjaro

Biological age is an estimate of the condition of cells and organs, distinct from the number of years someone has lived. Health conditions, smoking, diet, body weight and other aspects of life can influence the processes these estimates seek to capture.

Novo Nordisk used proteomic clocks. These analyse patterns in blood proteins to estimate age and mortality risk. Lilly used epigenetic clocks, which examine chemical markings associated with DNA rather than changes in the DNA sequence itself.

Both approaches offer ways to track molecular changes. A lower clock reading, however, is not equivalent to observing additional years of life. Nor does it establish that someone’s memory, mobility or independence has improved. Those are separate outcomes that require their own assessment.

Semaglutide mimics the action of GLP-1, a hormone involved in appetite and blood glucose regulation. Tirzepatide acts on both GLP-1 and GIP receptors. Their effects on appetite can help people eat less, while their effects on glucose regulation are important in treating type 2 diabetes.

The ageing research forms part of wider interest in the effects of GLP-1 medicines beyond weight loss. According to the Post, other studies have found improvements in blood pressure and cholesterol through a mixture of weight loss and mechanisms that do not depend on weight reduction.

That overlap leaves an important question: how much of a change in an ageing clock reflects better metabolic health, and how much represents a distinct effect on ageing? The report does not resolve this. As with research into GLP-1 medicines and inflammation, promising measurements need to be distinguished from established clinical benefits.

What ageing researchers and Lilly say about the findings

Steve Horvath, a geneticist known for developing ageing clocks, regarded the reported size of the effect as noteworthy. “Two years is a pretty strong effect, in my book,” he said, according to the Post.

Horvath interpreted the data as supporting the possibility that these medicines protect against biological ageing. That is an assessment of what the laboratory findings might mean, rather than evidence from a trial demonstrating longer survival.

Kevin Duffin, Lilly’s vice-president for ageing research, said the different clocks pointed towards a consistent reduction in estimated age. He also cautioned against expectations of a reversal amounting to decades.

The companies making the medicines presented the findings. The newspaper’s account does not supply a full trial-level assessment: it gives no exact follow-up duration, detailed uncertainty estimates or publication status for the analyses. Those omissions limit how closely readers can examine the strength and durability of the reported effects.

What the semaglutide research will test next

A separate research effort will examine outcomes that people can experience directly. The US agency ARPA-H is putting $38 million towards a study of whether semaglutide affects cognition, mobility and sensory acuity in healthy people over 60, the Post reported.

Studying healthy older adults addresses a gap in the company findings. Effects seen in people with obesity or type 2 diabetes cannot be assumed to occur in people without those conditions. The report does not give a start date or an expected date for results from the ARPA-H-funded work.

The balance of benefit and harm also remains relevant. These medicines can cause side effects and adverse events; a favourable change in a biological clock alone does not establish a reason for a healthy person to take them. For an anti-ageing claim to guide treatment, the unresolved questions concern not only molecular measurements, but meaningful benefits, their duration and the risks incurred in seeking them.

Why this matters

For patients already taking these medicines, the findings raise a credible research question about benefits beyond weight and blood glucose control. They do not yet provide a basis for choosing treatment to extend life. For healthy people considering such drugs, the distinction is more consequential: a laboratory estimate of younger biological age must be weighed against uncertain practical benefit and known treatment risks. Research measuring how people think, move and function will help determine whether the promise translates into healthier later life.

Frequently asked questions

Can Ozempic reverse ageing?
Company research suggests semaglutide may lower estimates of biological age. It does not establish that Ozempic reverses ageing throughout the body or extends life.
How much younger did people appear on biological ageing tests?
The reported reduction was around two to three years, although results varied by clock and organ. One measure based on heart-related proteins suggested a difference of as much as four years.
Was Mounjaro included in the ageing research?
Yes. Eli Lilly studied tirzepatide, sold as Mounjaro, using epigenetic clocks. Its study was smaller than Novo Nordisk’s semaglutide research, but the report did not give a participant count.
How many people were in the semaglutide ageing study?
Novo Nordisk analysed blood samples from 10,052 people. Half received semaglutide and half a placebo, with samples collected at the start and months later.
What are biological ageing clocks?
They are tools that estimate biological age from molecular measurements. The reported studies used patterns in blood proteins and DNA-associated chemical markings, rather than simply counting years lived.
Do weight-loss drugs slow ageing in healthy people?
That remains uncertain. The reported findings concerned people with excess weight or diabetes. ARPA-H is funding research into semaglutide’s effects on cognition, mobility and sensory acuity in healthy people over 60.
Do these studies prove that Ozempic helps people live longer?
No. The reported results concern biological clock readings, not demonstrated increases in lifespan. A lower estimated biological age is not the same as evidence that treatment extends life.

Sources

This report draws on the following original reporting:

Topics: Ozempic · Mounjaro · Biological ageing · Novo Nordisk · Eli Lilly

This article is for information only and is not medical advice.

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