SerpinA1 levels in amyotrophic lateral sclerosis patients: An exploratory study

Abstract

BackgroundSerpinA1, a serine protease inhibitor, is involved in the modulation of microglial‐mediated inflammation in neurodegenerative diseases. We explored SerpinA1 levels in cerebrospinal fluid (CSF) and serum of amyotrophic lateral sclerosis (ALS) patients to understand its potential role in the pathogenesis of the disease.MethodsSerpinA1, neurofilament light (NfL) and heavy (NfH) chain, and chitinase‐3‐like protein‐1 (CHI3L1) were determined in CSF and serum of ALS patients (n = 110) and healthy controls (n = 10) (automated next‐generation ELISA), and correlated with clinical parameters, after identifying three classes of progressors (fast, intermediate, slow). Biomarker levels were analyzed for diagnostic power and association with progression and survival.ResultsSerpinA1serum was significantly decreased in ALS (median: 1032 μg/mL) compared with controls (1343 μg/mL) (p = 0.02). SerpinA1CSF was elevated only in fast progressors (8.6 μg/mL) compared with slow (4.43 μg/mL, p = 0.01) and intermediate (4.42 μg/mL, p = 0.03) progressors. Moreover, SerpinA1CSF correlated with neurofilament and CHI3L1 levels in CSF. Contrarily to SerpinA1CSF, neurofilament and CHI3L1 concentrations in CSF correlated with measures of disease progression in ALS, while SerpinA1serum mildly related with time to generalization (rho = 0.20, p = 0.04). In multivariate analysis, the ratio between serum and CSF SerpinA1 (SerpinA1 ratio) and NfHCSF were independently associated with survival.ConclusionsHigher SerpinA1CSF levels are found in fast progressors, suggesting SerpinA1 is a component of the neuroinflammatory mechanisms acting upon fast‐progressing forms of ALS. Both neurofilaments or CHI3L1CSF levels outperformed SerpinA1 at predicting disease progression rate in our cohort, and so the prognostic value of SerpinA1 alone as a measure remains inconclusive.

Identification of key genes and signaling pathway in the pathogenesis of Huntington's disease via bioinformatics and next generation sequencing data analysis

“…Recent studies have shown that SERPINA1 [563], LRRK2 [522], CHRNA4 [564], CD22 [565], TF (transferrin) ssociated tyrosine kinase) [579], FGF14 [580], INSC (INSC spindle orientation adaptor protein) [581], BARHL1 [582], PRKCH (protein kinase C eta) [583], SLC24A4 [584], TMEM176B [585], MBP (myelin basic protein) [586], ACAN (aggrecan) [587], SHH (sonic hedgehog signaling molecule) [588], SIRT2 [589], RBP4 [590], ISM1 [591], HOXB6 [592], CDH13 [593], NTF3 [594], TRPC6 [595], MMP3 [596], HLA-DRB5 [597], HLA-DRB1 [546], CD74 [598], VWF (von Willebrand factor) [599], MDGA1 [600], ANGPT2 [601], NEDD4L [602], CASP1 [603], CHRNA5 [604], CCND2 [605], BRCA2 [606], TET1 [607], ZBTB20 [608], OAS1 [609], EGFR (epidermal growth factor receptor) [610], ABCA1 [611], PLXNA4 [612], FOXG1 [613], WEE1 [433], MAP1B [614], ANK1 [615], GRM3 [436], COMT (catechol-O-methyltransferase) [616], SLC10A4 [617], GPR39 [618] and LIFR (LIF receptor subunit alpha) [562] could promote Alzheimer’s disease progression. SERPINA1 [619], LRRK2 [620], CHRNA4 [621], TLR2 [622], MOBP (myelin associated oligodendrocyte basic protein) [623], AATK (apoptosis associated tyrosine kinase) [624], MBP (myelin basic protein) [625], SHH (sonic hedgehog signaling molecule) [626], XDH (xanthine dehydrogenase) [627], RBP4 [628], GRIA2 [629], NR3C2 [630], HLA-DRB5 [631], HLA-DRA [631], NEDD4L [632], CASP1 [633], EFNB2 [634], CYP7B1 [635], EGFR (epidermal growth factor receptor) [636], MAP1B [637], GRM3 [638<...…”