Study links rare CGAS gene variant to extended healthspan

Researchers have identified a rare genetic mutation that may help people from long-lived families stay healthier longer by reducing harmful inflammation. The findings were presented at the European Society of Human Genetics conference in Gothenburg.

Middle-aged people with long-lived parents developed cardiometabolic diseases an average of 13 years later than peers whose parents had shorter lifespans, according to the Leiden Longevity Study.

Scientists analyzed genomes from 212 long-lived sibships and pinpointed 12 rare protein-altering variants, including one in the CGAS gene found in two families. The variant appears to leave only one active copy of the gene, lowering inflammation while still allowing the body to fight infections.

Mr. Pasquale Putter of Leiden University Medical Center said the mutation could contribute to extended healthspan. Researchers plan to test its effects by introducing it into killifish at the Max Planck Institute for the Biology of Ageing in Cologne.

Professor Alexandre Reymond, conference chair, noted the work could help identify key factors for extending healthspan across the population.

Makala yanayohusiana

Conceptual illustration of gut bacteria producing inflammatory glycogen triggering brain inflammation in C9orf72-linked ALS and FTD, with stool sample comparisons and mouse treatment outcomes.
Picha iliyoundwa na AI

Study links microbial glycogen in the gut to inflammation in C9orf72-associated ALS and frontotemporal dementia

Imeripotiwa na AI Picha iliyoundwa na AI Imethibitishwa ukweli

Researchers at Case Western Reserve University report that some gut bacteria can make unusually inflammatory forms of glycogen and that this microbial glycogen can trigger immune activity linked to brain inflammation in models of disease tied to the C9orf72 mutation. In patient stool samples, the team found these glycogen forms more often in ALS and C9orf72-related frontotemporal dementia than in healthy controls, and enzymatically breaking down glycogen in the gut improved outcomes in mice.

Researchers at Israel's Weizmann Institute of Science have determined that genetics explain about 50% of differences in human lifespan, far more than previously estimated. The finding, published in the journal Science, challenges earlier views that placed genetic influence at 20-25% or less. By analyzing twin data and filtering out external death causes, the team uncovered this stronger hereditary role.

Imeripotiwa na AI

Researchers have discovered that mutations in the CD99L2 gene cause X-linked spastic ataxia, a rare movement disorder. The finding came from analysis of 2,811 patients with conditions affecting coordination and muscle control. The study was published in Nature Communications.

Doug Whitney, a US mechanic carrying a genetic mutation that typically triggers early-onset Alzheimer’s disease, has reached his late 70s without symptoms. Researchers link his protection to decades of intense heat exposure in ship engine rooms. The case bolsters evidence that heat therapy may safeguard the brain against the condition.

Tovuti hii inatumia vidakuzi

Tunatumia vidakuzi kwa uchambuzi ili kuboresha tovuti yetu. Soma sera ya faragha yetu kwa maelezo zaidi.
Kataa