Skip to main content

Or 34,00 After 66% tax deduction

I make a monthly donation I make an IFI donation
Research, science & health

Alzheimer disease: identification of a genetic marker

Published on: 29/05/2015 Reading time: 1 min
ADN

In a recent study of a large sample of Icelanders, researchers identified a correlation between the presence of a mutation on the gene ABCA7 and Alzheimer disease.

Iceland is a veritable laboratory for genetic research: founded more than a thousand years ago by a small number of explorers and still isolated to this day, the Icelandic population has very low genetic diversity, which facilitates the identification of relations between diseases and genetic mutations. In addition, the history of the population can be traced thanks to the quality of conserved genealogical data and the knowledge the inhabitants have of their origins.

In the study entitled "Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease," published on March 25, 2015, in Nature Genetics by several researchers, including Pr. Harald Hampel of Pierre and Marie Curie University / IMA2 / Institut du Cerveau - ICM, the scientists showed that an alteration in the gene ABCA7 might be a risk factor for Alzheimer's disease.

The ABCA7 protein is strongly expressed in the central nervous system and is part of a family of proteins involved in membrane transport.

The study was performed in a cohort of more than 2600 Icelanders, including healthy subjects and patients with various neurodegenerative disorders. The authors of the study include, notably, Pr. Harald Hampel, Kari Stefansson and his colleagues in deCODE Genetics, a subsidiary of Amgen based in Reykjavik.

The researchers also looked for genetic variants identified in cohorts of patients from other countries such as Germany, Finland, Norway and the USA, in which they were able to identify the same mutations in Alzheimer disease patients. The carriers of these rare variants had a mean 1.73 times greater probability of developing the disease.

According to Pr. Harald Hampel and the founder of deCIDE Genetics, Kari Stefansson, this study clearly demonstrates the power of the sequencing techniques.

At present, the researchers do not understand how the ABCA7 protein contributes to Alzheimer disease. But these studies open the way for new and more precise methods for diagnosing Alzheimer disease and other neurodegenerative disorders.

Pr. Harald Hampel occupies the AXA-UPMC Chair "Anticipate Alzheimer disease" at the Sorbonne Universities.

Our news on the subject

02 December 2024
Visuel of Scientific lectures
Scientific lectures: Michael GREICIUS
Speaker : Michael GREICIUS, Stanford medicine health care. "Reaching for high-hanging fruit in Alzheimer’s disease genetics"
11.12.2024 Scientific lectures
Interneurones. Crédit : UCLA Broad Stem Cell Research Center.
Stimulating specific neurons in the striatum stops compulsive behaviour
What if we could resist compulsions? These irrational behaviours, particularly common in obsessive-compulsive disorder (OCD), are hard to suppress. At Paris Brain Institute, Éric Burguière's team shows that we can anticipate them and block them...
09.10.2024 Research, science & health
Les nerfs moteurs présents dans la moelle épinière se projettent vers la périphérie, où ils entrent en contact avec les muscles, formant des connexions appelées jonctions neuromusculaires. Crédit : James N. Sleigh.
Ultrasound show unexpected effects on motor neuron disease
Over the past fifteen years, neurosurgeons have been perfecting a fascinating technique: using ultrasound to temporarily open the blood-brain barrier to facilitate the action of therapeutic molecules in the central nervous system. At Paris Brain...
09.05.2024 Research, science & health
Un neurone
Rett syndrome: a new gene therapy on the way
Gene therapy could be our best chance of treating Rett syndrome, a neurological disorder that causes severe intellectual and motor impairments. At Paris Brain Institute, Françoise Piguet and her colleagues have looked closely at brain cholesterol...
07.16.2024 Research, science & health
Lésions d’un patient à l’inclusion dans le protocole (M0) disparues après 2 ans de traitement à la Leriglitazone (M24)
The dual effect of leriglitazone in X-linked Adrenoleukodystrophy (X-ALD)
In 2023, the team led by Professor Fanny Mochel (AP-HP, Sorbonne University), a Paris brain Institute researcher, showed that daily dose of leriglitazone slow down the progression of myelopathy in patients with X-linked adrenoleukodystrophy, and...
06.28.2024 Research, science & health
Une tête de statue de l'île de Pâques sur laquelle sont posées des éléctrodes
A multimodal approach to better predict recovery in patients with disorders of consciousness
When a patient is admitted to intensive care due to a disorder of consciousness—such as a coma—establishing their neurological prognosis is a crucial yet challenging task. To reduce the uncertainty that precedes the medical decision, a group of...
05.30.2024 Research, science & health
See all our news