Association of complement receptor 1 gene polymorphisms with cognitive function
L E Zijlstra1, J W Jukema1, S P Mooijaart2
1Department of Cardiology, Leiden University Medical Center , Leiden , The Netherlands.
Physiological Genomics
|December 8, 2017
Summary
Genetic variations in the complement receptor 1 (CR1) gene are linked to cognitive decline in older adults. This research highlights CR1
Area of Science:
- Genetics
- Neuroscience
- Gerontology
Background:
- The complement receptor 1 (CR1) gene has been implicated in the development of Alzheimer's disease.
- Understanding the role of CR1 in cognitive function is crucial for addressing age-related cognitive decline.
Purpose of the Study:
- To investigate the association between CR1 gene single nucleotide polymorphisms (SNPs) and cognitive function in an elderly population.
- To determine if CR1 genetic variations impact general cognitive function beyond Alzheimer's disease.
Main Methods:
- Assessed 73 single nucleotide polymorphisms (SNPs) within the CR1 gene region on chromosome 1 in 5,244 elderly participants.
- Utilized linear regression analysis, adjusting for age, sex, country, and pravastatin use, to examine SNP-cognitive function associations.
- Identified 18 independent CR1 SNPs based on linkage disequilibrium.
Main Results:
- Twelve of the 18 independent CR1 SNPs were significantly associated with a decline in cognitive function (P < 0.05).
- These findings suggest a broader role for CR1 in cognitive health during late life.
Conclusions:
- Genetic variations within the CR1 gene are associated with general cognitive function in older individuals.
- The CR1 gene may serve as a potential target for understanding and mitigating cognitive decline in aging populations.
Related Concept Videos
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
10
Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
10
Human Genetics
1.7K
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
The complex relationship between genetics and psychology is observable through common biological components such...
1.7K
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
18
Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
18
Pharmacogenomics: Identification of New Drug Targets
10
Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
10
Complementation Tests
6.3K
A complementation test is a simple cross to identify whether the two mutations are located on the same gene or different genes. It was first performed by Edward Lewis in the 1940s while working on fruit flies. He developed the test to identify the location and arrangement of different mutations on chromosomes.
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...
Organisms heterozygous for different mutations are crossed pairwise in all combinations. If present on different genes, the mutations can complement each other by providing the missing...
6.3K
Principles of Pharmacogenetics: Types of Genetic Variants
14
The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...
14


