NAAA, N-acylethanolamine acid amidase, 27163

N. diseases: 90; N. variants: 6
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. 31320639 2019
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.050 Biomarker phenotype BEFREE In conclusion, the PLT-F demonstrated excellent performance for diagnosis of thrombocytopenia and for platelet transfusion guidance in the evaluated specimens from acute leukemia patients. 30761915 2019
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.050 GeneticVariation phenotype BEFREE Severe thrombocytopenia (PLT < 20 × 10<sup>9</sup>/L), identified in 31 (26.5%) patients, was associated with poor survival. 30296835 2018
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.050 Biomarker phenotype BEFREE The meta-analyses suggested there was a significantly higher overall response rate (OR 1.89; CI: 1.10-3.24; p = 0.02), grades of KPS (OR 2.35; CI: 1.55-3.56; p<0.01), CD3+cells (MD 10.29; CI: 8.46-12.12; p<0.01), CD4+cells (MD 7.06; CI: 5.33-8.794; p<0.01), CD4/CD8+cells (MD 0.32; CI: 0.25-0.40; p<0.01), NK+ (MD 7.20; CI: 2.02-12.37, p = 0.006), WBC (MD 1.24; CI: 0.59-1.89; p<0.01), HB (MD 14.55; CI: 7.47-21.63; p<0.01), and PLT (MD 19.05; CI: 4.29-33.81; p = 0.01), but lower severe toxicity for leukocytopenia (OR 0.37; CI: 0.17-0.80; p = 0.01), thrombocytopenia (OR 0.32; CI: 0.14-0.74; p = 0.008), gastrointestinal toxicity (OR 0.48; CI: 0.24-0.96; p = 0.04), when chemotherapy combined with SFI was compared with chemotherapy alone. 28953950 2017
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.050 GeneticVariation phenotype BEFREE Thrombocytopenia (PLT < 15 x 10(4)/microL) in type C cirrhosis was diagnosed in all patients with an intact spleen, 8 patients submitted to splenectomy, and in 19 non-C cirrhosis with intact spleen. 16534872 2006
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia
0.050 GeneticVariation phenotype BEFREE Recombinant FVIIa (rFVIIa) has been shown to improve hemostasis in patients with thrombocytopenia and to prevent or control bleeding episodes in patients with inherited deficiencies of major PLT glycoproteins, but the mechanism of action is not well understood. 12823748 2003
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE The disclosed cyanamides represent promising new pharmacological tools to investigate the potential role of NAAA inhibitors and dual NAAA-FAAH inhibitors as therapeutic agents for the treatment of inflammation and pain. 31761726 2020
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE The results revealed that NAAA may has been implicated in OA progression, and treatment with NAAA inhibitor F215 alleviated OA development by preventing cartilage damage, reducing inflammation, and alleviating pain. 31063807 2019
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE Recent medicinal chemistry efforts have led to the development of potent and stable inhibitors that enable studying the effects of NAAA inhibition in preclinical disease models, notably in the context of pain and inflammation. 29567427 2018
CUI: C0030193
Disease: Pain
Pain
0.040 Biomarker phenotype BEFREE The findings further suggest that NAAA regulates peripheral pain initiation by interrupting endogenous FAE signaling at PPAR-α. 23218523 2013
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.020 Biomarker disease BEFREE <b>Conclusion:</b> Collectively, PLT-Exo overexpressing miR-25-3p attenuates ox-LDL-induced CVEC inflammation in ApoE<sup>-/-</sup> mouse models of atherosclerosis. 31632389 2019
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.020 Biomarker disease BEFREE <b>Conclusion:</b> Collectively, PLT-Exo overexpressing miR-25-3p attenuates ox-LDL-induced CVEC inflammation in ApoE<sup>-/-</sup> mouse models of atherosclerosis. 31632389 2019
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.020 Biomarker disease BEFREE Changes in PLT between patients with and without cirrhosis were not significantly different at any of the time points. 31365178 2019
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.020 AlteredExpression disease BEFREE Univariate analysis showed that age, weight, high AST level, low PLT level, and smoking were the risk factors associated with liver fibrosis in the smokers with NAFLD while multivariate analysis showed that age (OR = 1.029, <i>P</i>=0.021), high AST level (OR = 1.0121, <i>P</i>=0.025), and smoking (OR = 1.294, <i>P</i>=0.015) were the independent risk factors associated with liver fibrosis in the patients with NAFLD. 31737583 2019
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.020 Biomarker disease BEFREE This suggests that changes in PLT post-viral elimination should not be interpreted as being reflective of changes in liver fibrosis or portal hypertension. 31365178 2019
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.020 Biomarker disease BEFREE Changes in PLT between patients with and without cirrhosis were not significantly different at any of the time points. 31365178 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE Patients with PLT <40 ×109/l, PT prolonged >3 s and malignancy had inferior survival. 29025045 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE In addition, we found that the PTT treatment augmented PLT-AuNRs targeting to the tumor sites and in turn, improved the PTT effects in a feedback manner, demonstrating the unique self-reinforcing characteristic of PLT-PTT in cancer therapy. 29193651 2018
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 Biomarker group BEFREE In addition, we found that the PTT treatment augmented PLT-AuNRs targeting to the tumor sites and in turn, improved the PTT effects in a feedback manner, demonstrating the unique self-reinforcing characteristic of PLT-PTT in cancer therapy. 29193651 2018
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 Biomarker group BEFREE In addition, we found that the PTT treatment augmented PLT-AuNRs targeting to the tumor sites and in turn, improved the PTT effects in a feedback manner, demonstrating the unique self-reinforcing characteristic of PLT-PTT in cancer therapy. 29193651 2018
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 Biomarker group BEFREE Patients with PLT <40 ×109/l, PT prolonged >3 s and malignancy had inferior survival. 29025045 2018
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.020 Biomarker disease BEFREE The association between hs-CRP, WBC, LDL, PLT, fibrinogen, creatinine, and the amount of periodontopathogenic microorganisms indicates the possibility that periodontal treatment could decrease the risk atherosclerosis. 28116969 2017
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.020 Biomarker disease BEFREE The association between hs-CRP, WBC, LDL, PLT, fibrinogen, creatinine, and the amount of periodontopathogenic microorganisms indicates the possibility that periodontal treatment could decrease the risk atherosclerosis. 28116969 2017