Details

Autor(en) / Beteiligte

• Piccio, Laura
• Deming, Yuetiva
• Del-Águila, Jorge L.
• Ghezzi, Laura
• Holtzman, David M.
• Fagan, Anne M.
• Fenoglio, Chiara
• Galimberti, Daniela
• Borroni, Barbara
• Cruchaga, Carlos

Titel

Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status

Ist Teil von

• Acta neuropathologica, 2016-06, Vol.131 (6), p.925-933

Ort / Verlag

Berlin/Heidelberg: Springer Berlin Heidelberg

Erscheinungsjahr

2016

Quelle

MEDLINE

Beschreibungen/Notizen

• Low frequency coding variants in TREM2 are associated with increased Alzheimer disease (AD) risk, while loss of functions mutations in the gene lead to an autosomal recessive early-onset dementia, named Nasu-Hakola disease (NHD). TREM2 can be detected as a soluble protein in cerebrospinal fluid (CSF) and plasma, and its CSF levels are elevated in inflammatory CNS diseases. We measured soluble TREM2 (sTREM2) in the CSF of a large AD case–control dataset ( n  = 180) and 40 TREM2 risk variant carriers to determine whether CSF sTREM2 levels are associated with AD status or mutation status. We also performed genetic studies to identify genetic variants associated with CSF sTREM2 levels. CSF, but not plasma, sTREM2 was highly correlated with CSF total tau and phosphorylated-tau levels ( r  = 0.35, P  < 1×10 −4 ; r  = 0.40, P  < 1×10 −4 , respectively), but not with CSF Aβ42. AD cases presented higher CSF sTREM2 levels than controls ( P  = 0.01). Carriers of NHD-associated TREM2 variants presented significantly lower CSF sTREM2 levels, supporting the hypothesis that these mutations lead to reduced protein production/function (R136Q, D87N, Q33X or T66M; P  = 1×10 −3 ). In contrast, CSF sTREM2 levels were significantly higher in R47H carriers compared to non-carriers ( P  = 6×10 −3 ), suggesting that this variant does not impact protein expression and increases AD risk through a different pathogenic mechanism than NHD variants. In GWAS analyses for CSF sTREM2 levels the most significant signal was located on the MS4A gene locus ( P  = 5.45 × 10 −07 ) corresponding to one of the SNPs reported to be associated with AD risk in this locus. Furthermore, SNPs involved in pathways related to virus cellular entry and vesicular trafficking were overrepresented, suggesting that CSF sTREM2 levels could be an informative phenotype for AD.