2013
DOI: 10.1016/j.gene.2013.08.016
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Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population

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Cited by 15 publications
(13 citation statements)
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“…This principle is evidenced by a case-report [81] of a patient diagnosed with pernicious anemia at age 16 who later developed AA at age 24, and another report [73] of a patient who developed type 1 diabetes at age 18, 9 months later developed AA, and at age 27 was diagnosed with pernicious anemia. However, as mentioned previously, available case-control studies [72, 79, 80] with multiple AA cases did not identify any such differences in B 12 levels in patients compared to controls.…”
Section: Micronutrientsmentioning
confidence: 69%
See 1 more Smart Citation
“…This principle is evidenced by a case-report [81] of a patient diagnosed with pernicious anemia at age 16 who later developed AA at age 24, and another report [73] of a patient who developed type 1 diabetes at age 18, 9 months later developed AA, and at age 27 was diagnosed with pernicious anemia. However, as mentioned previously, available case-control studies [72, 79, 80] with multiple AA cases did not identify any such differences in B 12 levels in patients compared to controls.…”
Section: Micronutrientsmentioning
confidence: 69%
“…Interestingly, in one AA genetic study, Kalkan et al [80] found that AA patients compared to controls had a higher prevalence of the C677T polymorphism (CT or TT vs. CC genotype) for the enzyme methylenetetrahydrofolate reductase (MTHFR), a key regulator of folate metabolism. The same polymorphism has been associated with other immune-mediated diseases including Graves’ disease [82] and multiple sclerosis [83].…”
Section: Micronutrientsmentioning
confidence: 99%
“…A study including 29 patients with AA that involved > 20% of the scalp showed that mean red blood cell folate concentrations were significantly lower in the patient group than in controls and significantly lower in patients with alopecia totalis/alopecia universalis than in patients with patchy hair loss [ 46 ]. Of interest, a genetic study including 136 Turkish patients with AA and 130 healthy controls found that the affected patients had a higher prevalence of mutations in the methylene-tetrahydrofolate reductase (MTHFR) gene [ 47 ]. This gene regulates folate metabolism, influences nucleic acid synthesis and DNA methylation, and is associated with other autoimmune disorders.…”
Section: Vitamin Bmentioning
confidence: 99%
“…These results suggest that mutations in MTHFR might impact the risk of AA in the Turkish population. However, there was no difference between serum levels of folate or vitamin B12 in affected patients and controls [ 47 ].…”
Section: Vitamin Bmentioning
confidence: 99%
“…But for MTR A2756G and MTRR A66G polymorphisms, there are not enough studies. Hence, further studies are need to be conducted (Table 1) [39][40][41][42][43][44][45][46][47][48][49][50][51][52][53][54][55][56][57][58]. …”
Section: Genetic Susceptibility and The Risk Of Msmentioning
confidence: 99%