AI Article Synopsis

  • Alzheimer's disease (AD) is a neurodegenerative condition leading to cognitive decline and significantly impacting quality of life, particularly in individuals over 65 years old.
  • The study examined specific genes to determine their role in late-onset Alzheimer's disease (LOAD) and assessed their potential as biomarkers for early diagnosis and treatment.
  • Results showed no difference in expression levels for some genes between patients and controls, while two specific genes had significantly lower expression in patients, suggesting their potential as diagnostic biomarkers for LOAD.

Article Abstract

Alzheimer's disease (AD) is a neurodegenerative disease that is characterized by a devastating decline in cognitive activities among all types of dementia, and it severely affects the quality of life. Late-onset AD (LOAD) occurs after the age of 65 years and develops sporadically. Although aging comes first along the main risk factors underlying LOAD, disease-causing susceptibility genes have been associated with disease pathogenesis. In our study, we included the genes , , , , , and to be investigated in LOAD patients based on their expression levels. Within this framework, we aimed to determine the possible functions of these genes in the pathophysiology of the disease. We investigated whether the utilization of these genes as biomarkers in the early diagnosis of LOAD may help the treatment scheme to be applied in the clinic. We involved 50 individuals in the study and collected peripheral blood samples from the patients and control groups for molecular genetic analysis. Subsequently, RNA was extracted from the peripheral blood samples, and expression analyzes were performed using qualitative reverse transcription polymerase chain reaction. The results obtained were evaluated by using proper statistical methods. Our results demonstrated that there was no difference between patient and control groups in terms of , , , and genes. The expression levels of the and genes were significantly lower in the patient group compared with the control group. In conclusion, we presume that the and genes can be utilized as molecular biomarkers for LOAD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9192179PMC
http://dx.doi.org/10.1055/s-0042-1743570DOI Listing

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