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Immunity gene IFITM3 variant: Relation to cognition and Alzheimer's disease pathology.
Pyun, Jung-Min; Park, Young Ho; Hodges, Angela; Jang, Jae-Won; Bice, Paula J; Kim, SangYun; Saykin, Andrew J; Nho, Kwangsik.
Affiliation
  • Pyun JM; Department of Neurology Seoul National University Bundang Hospital and Seoul National University College of Medicine Seongnam Republic of Korea.
  • Park YH; Department of Neurology Soonchunhyang University Seoul Hospital Soonchunhyang University College of Medicine Seoul Republic of Korea.
  • Hodges A; Department of Neurology Seoul National University Bundang Hospital and Seoul National University College of Medicine Seongnam Republic of Korea.
  • Jang JW; Institute of Psychiatry Psychology & Neuroscience King's College London London UK.
  • Bice PJ; Department of Neurology Kangwon National University Hospital Chuncheon Republic of Korea.
  • Kim S; Department of Radiology and Imaging Sciences, and the Indiana Alzheimer Disease Center Indiana University School of Medicine Indianapolis Indiana USA.
  • Saykin AJ; Department of Neurology Seoul National University Bundang Hospital and Seoul National University College of Medicine Seongnam Republic of Korea.
  • Nho K; Department of Radiology and Imaging Sciences, and the Indiana Alzheimer Disease Center Indiana University School of Medicine Indianapolis Indiana USA.
Alzheimers Dement (Amst) ; 14(1): e12317, 2022.
Article in En | MEDLINE | ID: mdl-35769874
ABSTRACT

Introduction:

We investigated single-nucleotide polymorphisms (SNPs) in IFITM3, an innate immunity gene and modulator of amyloid beta in Alzheimer's disease (AD), for association with cognition and AD biomarkers.

Methods:

We used data from the Alzheimer's Disease Neuroimaging Initiative (ADNI; N = 1565) and AddNeuroMed (N = 633) as discovery and replication samples, respectively. We performed gene-based association analysis of SNPs in IFITM3 with cognitive performance and SNP-based association analysis with cognitive decline and amyloid, tau, and neurodegeneration biomarkers for AD.

Results:

Gene-based association analysis showed that IFITM3 was significantly associated with cognitive performance. Particularly, rs10751647 in IFITM3 was associated with less cognitive decline, less amyloid and tau burden, and less brain atrophy in ADNI. The association of rs10751647 with cognitive decline and brain atrophy was replicated in AddNeuroMed.

Discussion:

This suggests that rs10751647 in IFITM3 is associated with less vulnerability for cognitive decline and AD biomarkers, providing mechanistic insight regarding involvement of immunity and infection in AD. Highlights IFITM3 is significantly associated with cognitive performance.rs10751647 in IFITM3 is associated with cognitive decline rates with replication.rs10751647 is associated with amyloid beta load, cerebrospinal fluid phosphorylated tau levels, and brain atrophy.rs10751647 is associated with IFITM3 expression levels in blood and brain.rs10751647 in IFITM3 is related to less vulnerability to Alzheimer's disease pathogenesis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Alzheimers Dement (Amst) Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Alzheimers Dement (Amst) Year: 2022 Type: Article