2014
DOI: 10.1016/j.ejmhg.2014.03.003
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Haptoglobin phenotypes as a risk factor for coronary artery disease in type 2 diabetes mellitus: An Egyptian study

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Cited by 10 publications
(12 citation statements)
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“…Hp1 exerts greater antioxidant activity than Hp2, with various studies confirming the association with higher oxidative stress and diabetic complications [ 123 ]. All reported studies similarly confirmed the association with prevalence of CAD, MI or MACE in T2DM [ 121 , 122 , 124 , 125 ] (Table 4 ).…”
Section: Polymorphisms Of Heme System Genessupporting
confidence: 66%
See 1 more Smart Citation
“…Hp1 exerts greater antioxidant activity than Hp2, with various studies confirming the association with higher oxidative stress and diabetic complications [ 123 ]. All reported studies similarly confirmed the association with prevalence of CAD, MI or MACE in T2DM [ 121 , 122 , 124 , 125 ] (Table 4 ).…”
Section: Polymorphisms Of Heme System Genessupporting
confidence: 66%
“…Hp is a serum α 2 -glycoprotein, an acute phase reactant synthetized mainly in the liver. Free heme is bound by the Hp stabilizing iron within, and consequently prevents oxidative stress damage [ 121 ]. In humans, there are two alleles of Hp, Hp1 and Hp2 [ 122 ].…”
Section: Polymorphisms Of Heme System Genesmentioning
confidence: 99%
“…Indeed, a number of studies have associated Hp phenotypes with the development or progression of diseases, and the antioxidant activities of the phenotypes have been proposed as the underlying mechanism of the association . In type 2 diabetes, Hp2‐2 was considered to be a major susceptible gene for the development of coronary artery disease (CAD); it correlates with increased levels of inflammatory response markers . The Hp2‐2 phenotype has been implicated in increased HIV viral titres compared to the other Hp phenotypes .…”
Section: Discussionmentioning
confidence: 99%
“…Hp0 is the absence of Hp in blood, which has been attributed to mutation and/or deletion of the promoter region of the HP gene and excessive haemolysis, and results in null expression and rapid clearance of the circulatory protein, respectively . Different Hp phenotypes have been associated with different diseases due to disparities in free radical clearance by the respective phenotypes . Poor clearance of free haemoglobin (Hb) in circulation by Hp2‐2 phenotype increases iron availability for growth of iron‐dependent bacteria , and the phenotype has also been reported to increase mortality rate of HIV‐infected patients compared to Hp1‐1 and Hp2‐1 .…”
Section: Introductionmentioning
confidence: 99%
“…Именно альфа-цепь может существовать в двух аллельных формах: альфа 1 (83 аминокислотных остатка, укороченная форма) и альфа 2 (142 аминокислотных остатка, полноразмерная форма). Таким образом, одной из причин сниженного содержания белка может быть аллельный полиморфизм, который ассоциируют с развитием различных заболеваний различных органов, в том числе сердечно-сосудистой системы [14,15]. Метод MRM позволяет отслеживать и принимать во внимание как артефакты пробоподготовки, так и структурные различия аминокислотной последовательности, обусловленные точечными мутациями или посттрансляционными модификациями.…”
Section: протеомное ядро плазмы крови человека: оценка межиндивидуальunclassified