PLA2G1B, phospholipase A2 group IB, 5319

N. diseases: 268; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.350 GeneticVariation disease BEFREE Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1. 9149325 1996
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.350 Biomarker disease PSYGENET Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1. 9149325 1996
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.350 Biomarker disease PSYGENET We have found evidence of an allelic association between bipolar disorder and a marker at the pancreatic phospholipase A2 gene (PLA2A) in this region (p < or = 0.01). 8750360 1995
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.350 GeneticVariation disease BEFREE We have found evidence of an allelic association between bipolar disorder and a marker at the pancreatic phospholipase A2 gene (PLA2A) in this region (p < or = 0.01). 8750360 1995
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.320 Biomarker group BEFREE In the present study, the possible association between the PLA2 gene and unipolar affective disorder was examined on 321 unipolar patients and 604 controls (all personally interviewed), recruited from six countries (Belgium, Bulgaria, Croatia, Germany, Greece, and Italy) participating in the European Collaborative Project on Affective Disorders. 14639048 2003
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.320 Biomarker group PSYGENET These findings suggest that structural variations at the PLA2 gene or the chromosomal region around it may confer susceptibility for unipolar affective disorder. 14639048 2003
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.320 Biomarker group BEFREE The maximum evidence for linkage was given by a polymorphism at the gene encoding secretory phospholipase A2 (PLA2A), a candidate gene for affective disorder.Dawson et al. 9149325 1996
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
0.320 Biomarker group PSYGENET The maximum evidence for linkage was given by a polymorphism at the gene encoding secretory phospholipase A2 (PLA2A), a candidate gene for affective disorder.Dawson et al. 9149325 1996
CUI: C0338715
Disease: Drug-induced depressive state
Drug-induced depressive state
0.300 Biomarker disease PSYGENET Phospholipase A2 and cyclooxygenase 2 genes influence the risk of interferon-alpha-induced depression by regulating polyunsaturated fatty acids levels. 20034614 2010
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Among all the existing isoforms, secretory PLA2 is the major target for inhibitor development, since many studies have proven that this enzyme participates in various inflammatory conditions, such as cancer, Alzheimer and arthritis. 30706775 2020
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE Analysis of PLA2R-AB in longitudinal serum samples revealed seropositivity in 44% (59 out of 134) of primary MN cases, 3% (one out of 35) of secondary MN cases, and in 0% of healthy controls. 31843984 2020
Idiopathic Membranous Glomerulonephritis
0.100 Biomarker disease BEFREE Diagnostic efficacy of serum anti-phospholipase A2 receptor antibodies for idiopathic membranous nephropathy in patients with diabetic kidney disease. 31730818 2020
Idiopathic Membranous Glomerulonephritis
0.100 Biomarker disease BEFREE Relationship between the status of phospholipase A2 receptor and prognosis of idiopathic membranous nephropathy. 31226230 2020
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.100 Biomarker disease BEFREE Bee Venom Soluble Phospholipase A2 Exerts Neuroprotective Effects in a Lipopolysaccharide-Induced Mouse Model of Alzheimer's Disease <i>via</i> Inhibition of Nuclear Factor-Kappa B. 31736738 2019
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.100 Biomarker disease BEFREE The first part of this review article focuses on the role of pancreatic-derived PLA2G1B in mediating lipid absorption and discusses how the PLA2G1B-derived metabolic product contributes to cardiometabolic diseases, including obesity, hyperinsulinemia, hyperlipidemia, and atherosclerosis. 30003964 2019
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.100 Biomarker disease BEFREE The first part of this review article focuses on the role of pancreatic-derived PLA2G1B in mediating lipid absorption and discusses how the PLA2G1B-derived metabolic product contributes to cardiometabolic diseases, including obesity, hyperinsulinemia, hyperlipidemia, and atherosclerosis. 30003964 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Several recent studies revealed that phospholipid metabolising enzyme, phospholipase A2 (PLA<sub>2</sub>), is a critical regulator of cancer accelerating pathologies and apoptosis in several types of cancers. 29104026 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Finally, recent studies revealing a relationship between PLA2G1B and cancer will also be discussed. 30003964 2019
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.100 Biomarker disease BEFREE Exploring calcium ion-dependent effect on the intermolecular interaction between human secreted phospholipase A2 and its peptide inhibitors in coronary artery disease. 31536875 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 Biomarker disease BEFREE Exploring calcium ion-dependent effect on the intermolecular interaction between human secreted phospholipase A2 and its peptide inhibitors in coronary artery disease. 31536875 2019
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE While there is an increasing understanding of primary MN with the discovery of antibodies directed against phospholipase A2 receptor (PLA2R Ab) and thrombospondin type 1 domain-containing 7A, circulatory factors causative of inducing MCD and FSGS remain in part elusive. 31447217 2019
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE The discovery in 2009 of the M-type phospholipase A2 receptor (PLA2R) as the primary target in membranous nephropathy (MN) greatly advanced basic and clinical research. 31611068 2019
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE Autoantibodies both to the M-type phospholipase A2 receptor (PLA2R) and to thrombospondin type-1 domain-containing 7A (THSD7A), initially described in adult MN, have now been identified in children and adolescents with MN and serve as a useful diagnostic and monitoring tool in this younger population as well. 31811540 2019
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE While the pathogenesis of MN is still controversial, the detection of autoantibodies against two specific glomerular antigens, phospholipase A2 receptor (PLA<sub>2</sub>R) and thrombospondin type 1 domain containing 7A (THSD7A), together with the beneficial effect of therapies targeting B cells, have highlighted the main role of autoreactive B cells driving this renal disease. 31788474 2019
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
0.100 Biomarker disease BEFREE Effect of belimumab on proteinuria and anti-phospholipase A2 receptor autoantibody in primary membranous nephropathy. 31243451 2019