Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 AlteredExpression disease BEFREE Significantly, compared to non-diabetics, BVRA and PKCζ expression was low and haptoglobin was high in T2D patients leukocytes. 31065010 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE In adults with type 2 diabetes the haptoglobin genotype 1-1 has been shown to have a protective role in inhibiting the development of complications. 17939622 2007
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE This study investigated the possible association of haptoglobin genotypes with onset of retinopathy in Type 2 diabetes (DM2). 21555971 2011
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 AlteredExpression disease BEFREE An Okinawan-based Nordic diet improves glucose and lipid metabolism in health and type 2 diabetes, in alignment with changes in the endocrine profile, whereas zonulin levels are elevated. 30936958 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE The haptoglobin 2 allele was determined to be a risk factor for type 2 diabetes in Ghana (OR = 6.1, 95% CI = 1.8-21.2; P = .0.001) while the Hp1 allele appeared protective (OR = 0.56, 95% CI = 0.31-1.0; P = .06). 16733296 2006
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Haptoglobin 1-1 Genotype Modulates the Association of Glycemic Control With Hippocampal Volume in Elderly Individuals With Type 2 Diabetes. 28860127 2017
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE Haptoglobin genotype modulates the relationships of glycaemic control with cognitive function in elderly individuals with type 2 diabetes. 25628235 2015
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE A positive correlation was observed between Zo and LPS in T2DM-CKD subjects. 28925931 2017
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Author Correction: Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. 30190539 2018
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE When combined with the glycation level of lysine-141 of haptoglobin, diagnostic accuracy improved further for newly diagnosed (SN, 94%; SP 96%) and long-term controlled (SN, 85%; SP, 94%) T2DM patients (HbA1c: SN, 88%; SP, 96%). 29943387 2018
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE Haptoglobin(Hp) 2-2 genotype has been shown to increase coronary artery disease (CAD) risk in numerous type 2 diabetes studies but in only one type 1 diabetes cohort. 27539884 2018
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE The present paper reports the results of tests of association between Type 2 diabetes mellitus and seven polymorphic markers: the blood groups - ABO, Rhesus, Duffy and Kell (K and KP) - haptoglobin and group specific component; among Anglo and Hispanic populations in the San Luis Valley of Colorado, USA. 2792588 1989
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE Haptoglobin genotypes and refractory hypertension in type 2 diabetes mellitus patients. 22011804 2011
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE The haptoglobin 2-2 genotype is associated with atherosclerosis in type 2 diabetes mellitus. 27190085 2016
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 AlteredExpression disease BEFREE Serum Hp levels in T2DM patients and non-DM subjects were 103.40 (72.46, 131.99) mg/dL and 100.20 (53.99, 140.66) mg/dL, respectively. 30634984 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE The genetic polymorphism of haptoglobin (HP) has been associated with cardiovascular disease and type 2 diabetes. 18760271 2008
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Urine Haptoglobin/Creatinine Ratio Correlates with Tubular Injury Biomarkers and Severity of Albuminuria in Type 2 Diabetes Patients. 31505705 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Haptoglobin (Hp), a major antioxidant protein, is a determinant of cardiovascular events in patients with Type 2 diabetes mellitus (DM). 18032779 2008
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE We investigated whether serum Hp has a causal effect on macroangiopathy via Mendelian randomization (MR) analysis with common variants of the Hp gene in Chinese patients with type 2 diabetes. 29338727 2018
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE The genetic variant rs2000999 was not associated with diabetic macrovascular diseases but showed an association with metabolic traits and serum Hp levels in Chinese patients with type 2 diabetes. 30366827 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE To collectively evaluate the association between haptoglobin (Hp) gene variants and diabetic retinopathy (DR) in patients with type 2 diabetes mellitus (T2DM). 28758129 2017
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. 29572449 2018
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE The Hp genotypes of 265 patients, 95 type 1 diabetes mellitus (DM1) sufferers with at least 10 years of disease and 170 type 2 diabetes mellitus (DM2) sufferers with at least 5 years of disease were determined by allele-specific PCR; both groups included patients with and without DN. 19455468 2009
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 Biomarker disease BEFREE Our findings suggest that serum Hp levels may be used as a potential biomarker for the early diagnosis and monitoring of DKD in T2DM patients. 31545979 2019
Entrez Id: 3240
Gene Symbol: HP
HP
0.600 GeneticVariation disease BEFREE <b>Conclusions:</b> These results suggest that subjects with type 2 diabetes carrying the Hp 1-1 genotype may have higher susceptibility to depression in the context of white matter damage and frontal lobe atrophy. 30809196 2019