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akaturk Akademik ölçüm

Makale detayı · 2016

Association between sequence variations of the Mediterranean fever gene and the risk of migraine a case ndash control study

Neuropsychiatric Disease and Treatment

YÖKSİS OpenAlex Açık erişim · gold SJR Q2 JCR Q3 Atıf 8 Yüzdelik 59.9% FWCI 0.15
Yıl
2016
ISSN
1178-2021
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

Migraine pathogenesis involves a complex interaction between hormones, neurotransmitters, and inflammatory pathways, which also influence the migraine phenotype. The Mediterranean fever gene (MEFV) encodes the pyrin protein. The major role of pyrin appears to be in the regulation of inflammation activity and the processing of the cytokine pro-interleukin-1β, and this cytokine plays a part in migraine pathogenesis. This study included 220 migraine patients and 228 healthy controls. Eight common missense mutations of the MEFV gene, known as M694V, M694I, M680I, V726A, R761H, K695R, P369S, and E148Q, were genotyped using real-time polymerase chain reaction with 5' nuclease assays, which include sequence specific primers, and probes with a reporter dye. When mutations were evaluated separately among the patient and control groups, only the heterozygote E148Q carrier was found to be significantly higher in the control group than in the patient group (P=0.029, odds ratio [95% confidence interval] =0.45 [0.21-0.94]). In addition, the frequency of the homozygote and the compound heterozygote genotype carrier was found to be significantly higher in patients (n=8, 3.6%) than in the control group (n=1, 0.4%) (P=0.016, odds ratio [95% confidence interval] =8.57 [1.06-69.07]). However, there was no statistically significant difference in the allele frequencies of MEFV mutations between the patients and the healthy control group (P=0.964). In conclusion, the results of the present study suggest that biallelic mutations in the MEFV gene could be associated with a risk of migraine in the Turkish population. Moreover, MEFV mutations could be related to increased frequency and short durations of migraine attacks (P=0.043 and P=0.021, respectively). Future studies in larger groups and expression analysis of MEFV are required to clarify the role of the MEFV gene in migraine susceptibility.

Konular

  • Inflammasome and immune disorders
  • Heme Oxygenase-1 and Carbon Monoxide
  • Neuroscience of respiration and sleep

Birincil konu Inflammasome and immune disorders

Yazarlar

  1. SALİH COŞKUN
  2. SEFER VAROL
  3. HASAN HÜSEYİN ÖZDEMİR
  4. sercan bulut çelik
  5. metin balduz
  6. camkurt mehmet akif
  7. ABDULLAH ÇİM
  8. DEMET ARSLAN
  9. MEHMET UĞUR ÇEVİK DİCLE ÜNİVERSİTESİ