2014
DOI: 10.7860/jcdr/2014/6342.4362
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Alpha-1 Antitrypsin, a Diagnostic and Prognostic Marker of Vernal Keratoconjunctivitis

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Cited by 4 publications
(5 citation statements)
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“…Lempinen also observed that the serum levels of the trypsin2-AAT complex were significantly higher in patients with SAP than patients with mild symptoms 44 . AAT was also elevated in many other diseases including vernal keratoconjunctivitis 20 , hepatic carcinoma, and severe chronic hepatitis 45 , reflecting the protective role of AAT in the tissue response to injury. Circulating AAT levels are reported to increase with greater inflammatory damage, indicating that AAT may represent a useful diagnostic or prognostic marker.…”
Section: Discussionmentioning
confidence: 99%
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“…Lempinen also observed that the serum levels of the trypsin2-AAT complex were significantly higher in patients with SAP than patients with mild symptoms 44 . AAT was also elevated in many other diseases including vernal keratoconjunctivitis 20 , hepatic carcinoma, and severe chronic hepatitis 45 , reflecting the protective role of AAT in the tissue response to injury. Circulating AAT levels are reported to increase with greater inflammatory damage, indicating that AAT may represent a useful diagnostic or prognostic marker.…”
Section: Discussionmentioning
confidence: 99%
“…AAT is reported to modulate systemic inflammatory responses, reducing production of pro-inflammatory cytokines, blocking leukocyte migration and inhibiting apoptosis 18 19 20 . However, the precise mechanisms governing regulation of serum AAT levels remain to be determined.…”
Section: Discussionmentioning
confidence: 99%
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“…Another study observed how alpha-1-antitrypsin levels in tears were lower in VKC rather than in the healthy control group [182]. Other potential biomarkers of VKC could be osteopontin and periostin concentrations in tears.…”
Section: Biomarkersmentioning
confidence: 98%
“…Tryptase activity was assayed using N-a-benzoyl-DL-arginine-p-nitroanilide as substrate [ 14 ], glutathione S-transferase (GSH) activity was assayed using 2,4-Dinitrochlorbenzene (CDNB) as substrate [ 15 ], chymotrypsin-like proteinase activity was assayed using N-succinyl-alanine-alanineproline-phenylalanine p-nitroanilide (SAAPFpNA) as substrate [ 16 ], and α-naphyle esterase activity was assayed using α-NA as substrate [ 17 ]. For the assessment of all protease activities, the absorbance was read at 410 nm using an Elx808 microplate reader (BioTek, USA).…”
Section: Methodsmentioning
confidence: 99%