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Rare Gene Variant Delays Alzheimer's Symptoms By Five Years

Neuropsychologist Yakeel Quiroz poses for this undated selfie in front of a imaging screen. (Yakeel Quiroz via AP)

Researchers studying a family with a history of early-onset Alzheimer's disease have uncovered a genetic anomaly that delays the onset of symptoms by up to five years. This discovery offers new possibilities for combating the debilitating effects of the disease, provided scientists can decipher how this rare gene variant provides some level of protection.

The breakthrough emerged during a study of a large Colombian family affected by an inherited form of Alzheimer's. One family member, Aliria Piedrahita de Villegas, defied expectations by experiencing cognitive decline in her 70s instead of her 40s, thanks to possessing a unique gene variant known as APOE3 Christchurch.

Further investigations identified 27 family members carrying a single copy of the protective Christchurch variant. These individuals, on average, exhibited cognitive symptoms five years later than their relatives without the variant, suggesting a potential delay in disease progression.

The findings, published in the New England Journal of Medicine, have sparked optimism among experts like Dr. Eliezer Masliah of the National Institute on Aging, who sees the possibility of leveraging this genetic insight to develop interventions that could slow down Alzheimer's onset.

Unique APOE3 Christchurch variant identified in family members with delayed cognitive decline.
Genetic anomaly in a Colombian family delays Alzheimer's symptoms by up to 5 years.
27 family members carrying the protective Christchurch variant show delayed disease progression.

Alzheimer's, affecting millions globally, typically strikes individuals over 65 years old. While age remains a primary risk factor, the APOE gene, with its various forms, also influences susceptibility to the disease. The APOE4 gene variant increases risk, while APOE2 appears to offer some protection. APOE3 was previously considered neutral until the discovery of the Christchurch variant's protective potential.

Research indicates that the Christchurch variant may impede the progression of Alzheimer's-related brain changes, such as the accumulation of amyloid protein and the formation of tau tangles that harm brain cells. While more investigation is needed to understand the precise mechanisms at play, scientists are exploring treatments that could mimic the protective effects of the rare gene variant.

Despite the complexity of Alzheimer's disease, this genetic discovery opens up promising avenues for developing targeted therapies that could alter the course of the illness. As researchers delve deeper into the impact of the Christchurch variant on Alzheimer's pathology, the hope is to unlock new strategies for combating this devastating condition.

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