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Record W4406209875 · doi:10.1002/alz.092899

Single nucleotide polimorphisms of the main glutamate transporter in the brain are associated with lower regional brain glucose metabolism in cognitively impaired individuals

2024· article· en· W4406209875 on OpenAlexaff
Christian Limberger, Luiza Santos Machado, Marco Antônio De Bastiani, Thomas Hugentobler Schlickmann, Giovanna Carello‐Collar, Guilherme Povala, Tharick A. Pascoal, Eduardo R. Zimmer

Bibliographic record

VenueAlzheimer s & Dementia · 2024
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicAmino Acid Enzymes and Metabolism
Canadian institutionsMcGill University
Fundersnot available
KeywordsTransporterGlutamate receptorMetabolismSingle-nucleotide polymorphismNucleotideExcitatory amino-acid transporterCarbohydrate metabolismEndocrinologyNeuroscienceInternal medicineMedicinePsychologyGeneticsBiologyGeneGenotype

Abstract

fetched live from OpenAlex

Abstract Background Astrocytes play a main role in brain energy metabolism, primarily through the metabolic cooperation with neurons. The use of [18F]fluorodeoxyglucose(FDG)‐PET has become a valuable indicator of neurodegeneration in Alzheimer's disease (AD), revealing a brain hypometabolic signature, but it is sensitive to changes in astrocyte metabolism. It is postulated that the activation of the excitatory amino acid transporter 2 (EAAT2) is the main trigger of FDG‐PET uptake in astrocytes. However, the potential relationship between single nucleotide polymorphisms (SNPs) in the gene that encodes for EAAT2 (SLC1A2) and the AD hypometabolic signature remains unknown. Here, we investigated whether SNPs in SLC1A2 affect brain glucose metabolism in cognitively impaired (CI) individuals. Method We assessed 331 CI individuals from the ADNI cohort with available [18F]FDG‐PET imaging data, CSF Aβ1‐42 and p‐tau181 measures, and genotyping data of SLC1A2 (Table 1). After the genetic data processing, 100 SNPs from the SLC1A2 gene were identified. In this study, we focused on the 10 SNPs more associated with [18F]FDG SUVR in an exploratory ROI‐wise analysis. Then, we performed voxel‐wise correlation analysis with RMINC, testing the association between the SLC1A2 SNP carriership and [18F]FDG‐PET, adjusting for age, sex, APOE4 status, and CSF Aβ42 and p‐tau181 levels (corrected p‐value < 0.05). Result Our findings revealed a negative association between four SLC1A2 SNPs and [18F]FDG‐PET in specific brain regions. This indicates that SLC1A2 SNP carriership is associated with lower regional glucose metabolism. Notably, rs57339940 carriers presented a significant cluster in the cingulate region (tmax = 3.04, p < 0.01, Figure 1A). Carriers of rs11033098 and rs11033099 exhibited bilateral clusters in areas of the lingual gyrus (tmax = 2.4806 and tmax = 2.8736, respectively, p < 0.01, Figure 1B‐C). Additionally, individuals with rs10768132 showed a substantial bilateral impact on the posterior areas of the cuneus (tmax = 2.9821, p < 0.01, Figure 1D). Conclusion These preliminary results show that SLC1A2 SNP carriership had a significant influence on regional glucose hypometabolism, specifically in areas comprising the occipital lobe and the cingulate region. Metabolic alterations may influence the susceptibility of those regions to accumulate amyloid in later stages of AD.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.005
Threshold uncertainty score0.012

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0040.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.017
GPT teacher head0.235
Teacher spread0.218 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2024
Admission routes1
Has abstractyes

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