Symposium

Of Rising Scholars

Fall 2024

Giselle will be presenting at The Symposium of Rising Scholars on Saturday, September 21st! To attend the event and see Giselle's presentation.

Go to Polygence Scholars page
Giselle Haddad's cover illustration
Polygence Scholar2024
Giselle Haddad's profile

Giselle Haddad

Class of 2025Bloomfield Hills, Michigan

About

Projects

  • "What impact do mutations in the TREM2 and CD33 genes have on the development of Alzheimer’s disease?" with mentor Tatiana (Aug. 14, 2024)

Project Portfolio

What impact do mutations in the TREM2 and CD33 genes have on the development of Alzheimer’s disease?

Started May 1, 2024

Abstract or project description

Alzheimer's disease (AD) is a complex neurodegenerative disorder characterized by the accumulation of amyloid plaques and neurofibrillary tangles. This study investigates the role of two key genes, TREM2 and CD33, in AD pathogenesis. Gene expression profiles from human brain samples and transgenic mouse models were analyzed using data from the Gene Expression Omnibus. Differential gene expression analysis revealed significant upregulation of TREM2 and CD33 in AD samples compared to controls. Analysis of KEGG pathway, a database composed of biological pathway maps, showed TREM2 involvement in osteoclast differentiation and CD33 in hematopoietic cell lineage. String database analysis highlighted both genes' roles in regulating tumor necrosis factor production and cytokine production. Furthermore, TREM2 variants in AD patients were examined, identifying six variants (H157Y, R98W, D87N, T66M, Y38C, and Q33X) exclusive to AD samples. The R47H variant showed the strongest correlation with AD (p<0.01). The following SNPs of CD33 were identified as contributors to AD development: rs3826656, rs3865444, and rs12459419. These findings suggest that TREM2 and CD33 play crucial roles in AD progression, potentially through modulation of microglial function and inflammatory responses. These genes may serve as promising targets for developing novel AD therapeutics and biomarkers.