Which biological aging markers best predict health decline? A 7-year study of 1,083 older adults

Researchers tested 16 different biomarkers of aging (epigenetic clocks, blood proteins, telomeres, and others) in over 1,000 people tracked for 7 years. Two markers—Allostatic Load Index and DunedinPACE—stood out as the most reliable predictors of …

53 Promising
Design 11
Sample 13
Peer Review 14
Replication 5
Transparency 10

Both genome instability and replicative senescence stem from the shortest telomere in telomerase-negative cells.

In the absence of telomerase, telomere shortening triggers replicative senescence, a tumor suppressor mechanism that is also associated with oncogenic genomic instability. Yet, the precise mechanism that connects these seemingly opposing forces remains poorly understood. …

47 Early
Design 5
Sample 7
Peer Review 19
Replication 6
Transparency 10

Dectin-1 epigenetic reprogramming rescues senescent-like Treg function in allergic asthma.

Allergic asthma is characterized by immune dysregulation, and deficiencies in regulatory T-cell (Treg) function are a hallmark of the disease. However, mechanisms of Treg impairment for their therapeutic correction remain poorly defined. The results showed …

46 Early
Design 5
Sample 7
Peer Review 18
Replication 6
Transparency 10

Dogs as aging models: A new study validates canine biomarkers of aging

Researchers enrolled 209 companion dogs in a 30-month study to identify biomarkers of aging that could make dogs a better translational model for human longevity research. Early findings show consistent age-related changes in blood work, …

50 Promising
Design 11
Sample 10
Peer Review 13
Replication 5
Transparency 11

How chemical marks on RNA control telomeres and aging

This review examines how chemical modifications to RNA molecules regulate telomere maintenance—the process that prevents chromosome shortening and cellular aging. The authors propose that understanding these epitranscriptomic controls could reveal new targets for treating aging-related …

28 Early
Design 4
Sample 2
Peer Review 11
Replication 2
Transparency 9

Reversing cell aging in stem cells using temporary genetic reprogramming

Researchers developed a method to rejuvenate aging mesenchymal stem cells (MSCs) by temporarily expressing three genes via a non-integrating virus, then removing the virus. The rejuvenated cells showed extended lifespan, restored telomeres, and maintained their …

39 Early
Design 5
Sample 6
Peer Review 14
Replication 5
Transparency 9

How mitochondrial DNA variants affect telomere length in human cells

Researchers used lab-grown cells to show that mitochondrial DNA variants affecting energy production influence telomere length by controlling reactive oxygen species and NAD levels. This suggests that inherited mitochondrial traits may influence how quickly our …

25 Early
Design 5
Sample 5
Peer Review 3
Replication 5
Transparency 7

DunedinPACE epigenetic clock best predicts cognitive decline in older adults

Researchers tested 14 different epigenetic clocks (DNA methylation–based age measures) in over 1,000 older adults and found that DunedinPACE, a newer clock, consistently predicted cognitive decline better than older clocks. This suggests DunedinPACE may be …

36 Early
Design 10
Sample 13
Peer Review 3
Replication 4
Transparency 6

A homozygote mutation in RPA2 associated with bone marrow failure, immunodeficiency, and telomere biology disorder.

Telomere biology disorders (TBDs) are characterized by bone marrow failure (BMF) and dysfunctional telomeres. So far, inherited mutations in 18 genes have been identified in TBDs. Here, we describe a child presenting with early BMF, …

38 Early
Design 5
Sample 7
Peer Review 10
Replication 6
Transparency 10

Immunosenescence in Human Disease: Mechanistic Insights and Therapeutic Opportunities.

Immunosenescence, an age-associated decline in immune function, is increasingly recognized as a central determinant of health and disease in older adults. Characterized by thymic involution, loss of naïve T cells, contraction of T cell receptor …

38 Early
Design 5
Sample 7
Peer Review 10
Replication 6
Transparency 10

No effect of education on Telomere Length: a natural experiment in aging individuals

Telomere length is increasingly used as a proxy for an aging exposome", an index of non-genetic environmental (and behavioral) exposures that an individual encounters, leading to differences in rates of aging. One of the largest …

39 Early
Design 5
Sample 7
Peer Review 4
Replication 6
Transparency 17

The Ess1 prolyl isomerase represses TERRA transcription and promotes telomere replication in Saccharomyces cerevisiae.

The conserved Ess1 prolyl isomerase (PIN1 in human) binds the carboxy-terminal domain (CTD) of RNA Pol II, and plays multiple roles in transcription regulation. Consistent with an essential role of the human PIN1 in telomere …

46 Early
Design 5
Sample 7
Peer Review 18
Replication 6
Transparency 10

Natural diversity of telomere length distributions across 100 Saccharomyces cerevisiae strains.

Telomeres gradually shorten at each cell division, and telomerase counteracts this shortening by elongating telomere sequences. This dynamic balance between elongation and shortening results in a steady-state telomere length (TL) distribution. Here, we develop a …

38 Early
Design 5
Sample 7
Peer Review 10
Replication 6
Transparency 10

Defying expectations: Extended lifespan and limited age-related telomere shortening in the tropical bat species, Molossus molossus.

Telomeres are key biomarkers of cellular ageing, yet their dynamics remain poorly studied in tropical and short-lived bat species. Here, we present the first investigation of telomere length across age in Molossus molossus, a tropical …

34 Early
Design 5
Sample 7
Peer Review 4
Replication 6
Transparency 12

Multimodal Ageing Biomarkers and Plasma Proteomic Signatures Associated with All-Cause Mortality

Ageing biomarkers can predict mortality risk beyond chronological age. Recently, plasma proteins were used to estimate the biological ages of eleven human organs, including the brain, heart, liver, kidneys, and pancreas. Accelerated organ ageing is …

34 Early
Design 5
Sample 7
Peer Review 4
Replication 6
Transparency 12

Integrative effects of Telomere Length, Epigenetic Age, and Mitochondrial DNA abundance in Alzheimer's Disease

Background and Objectives: Biological age, reflecting the cumulative molecular and cellular damage such as telomere attrition, epigenetic alterations and mitochondrial dysfunction, may better capture age-related decline and Alzheimer's disease (AD) risk than chronological age. Most …

34 Early
Design 5
Sample 7
Peer Review 4
Replication 6
Transparency 12

Mechanistic insights into aging and longevity: Implications for ovarian function and health.

Ovarian aging is characterized by progressive follicular reserve depletion, mitochondrial dysfunction, oxidative stress, and endocrine decline. This review examines the molecular mechanisms driving ovarian aging and evaluates emerging therapeutic strategies to preserve reproductive longevity. Key …

46 Early
Design 5
Sample 7
Peer Review 18
Replication 6
Transparency 10

Does Ginseng Slow Aging? A Small Study on Telomeres and Cellular Energy in Middle-Aged Adults

Researchers gave ginseng supplements to 50 overweight middle-aged adults in two groups and found associations with longer telomeres, higher NAD+ levels, and improvements in sleep and fatigue scores.

Researchers gave ginseng supplements to 50 overweight middle-aged adults in two groups and found associations with longer telomeres, higher NAD+ levels, and improvements in sleep and fatigue scores. However, the study is very small, lacks …

41 Early
Design 8
Sample 6
Peer Review 13
Replication 5
Transparency 9

DMTF1 Gene May Reverse Brain Aging in Neural Stem Cells

Researchers identified DMTF1, a transcription factor, as potentially therapeutic for reversing age-related decline in neural stem cell proliferation caused by telomere shortening. The mechanism involves DMTF1 regulating SWI/SNF chromatin complexes to activate E2F genes, a …

36 Early
Design 12
Sample 6
Peer Review 5
Replication 7
Transparency 6

Nine Core Mechanisms Explain Why We Age

This landmark review identifies nine interconnected biological processes—from DNA damage to stem cell failure—that drive aging across species. Rather than discovering new biology, it synthesizes existing knowledge into a unifying framework to guide future drug …

55 Promising
Design 4
Sample 2
Peer Review 19
Replication 16
Transparency 14