2020
DOI: 10.4103/ijd.ijd_104_18
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NPY gene polymorphism in vitiligo: A case–control study in Egyptian patients

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Cited by 5 publications
(4 citation statements)
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“…NPY, a 36 amino acid neuromodulator secreted by neurons, is believed to be involved in control of vitiligo development ( 7 , 21 , 38 , 39 ). Several studies have shown that the NPY levels of lesions and plasma in patients with vitiligo are significantly higher than in healthy volunteers ( 7 , 21 , 38 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…NPY, a 36 amino acid neuromodulator secreted by neurons, is believed to be involved in control of vitiligo development ( 7 , 21 , 38 , 39 ). Several studies have shown that the NPY levels of lesions and plasma in patients with vitiligo are significantly higher than in healthy volunteers ( 7 , 21 , 38 ).…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have shown that the NPY levels of lesions and plasma in patients with vitiligo are significantly higher than in healthy volunteers ( 7 , 21 , 38 ). Furthermore, NPY −399T/C (rs16147) and +1128T/C (rs16139) polymorphisms are correlated with vitiligo susceptibility and increase NPY transcription activity ( 39 , 40 ). In this study, we found that camouflage combined with psychotherapy could considerably decrease serum NPY level.…”
Section: Discussionmentioning
confidence: 99%
“…Skin neuroendocrinology literature has long suggested the involvement of NPY in skin pathology [47]. In support of this hypothesis, clinical studies have shown that genetic mutations in NPY are associated with increased susceptibility for vitiligo [48][49]. Studies have also shown that NPY is more highly expressed in the circulation and affected skin from patients suffering from atopic dermatitis and vitiligo [20][21][22][23][24][25]27].…”
Section: Discussionmentioning
confidence: 99%
“…In this case, the TC haplotype (+1128 T/-399 C) is associated with a 2.3-fold greater odds for developing vitiligo. Similarly, in an Egyptian population, the C/C and T/C genotypes of the -399T/C SNP are associated with a 3.75- and 4.6-fold increased odds for disease ( 103 ). Both the -399 and +1128 SNPs also appear to have functional consequences on NPY gene regulation.…”
Section: Genetic Associations Of Npy With Skin Pathologymentioning
confidence: 97%