Journals / Turkish Journal of Gastroenterology / 2009 / Cilt: 20 - Sayı: 3

Dispeptik yakınmaları olan Türk hastalarda CYP2C19 mutasyonlarının prevelansı

The prevalence of CYP2C19 mutations in Turkish patients with dyspepsia

Pages
161–164
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

This finding might have impact on the clinical consequences for the treatment strategies in dyspepsia.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background/aims: We aimed to determine the distribution of cytochrome P450 2C19 (CYP2C19) genotype frequencies in Turkish patients with dyspepsia.
📊
Key Findings & Data:Methods: CYP2C19 genotype was determined in 100 Turkish patients with dyspepsia.
💡
Conclusion & Impact:This finding might have impact on the clinical consequences for the treatment strategies in dyspepsia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Dispepsi · Hastalığa genetik yatkınlık · Genotip

Abstract

Background/aims: We aimed to determine the distribution of cytochrome P450 2C19 (CYP2C19) genotype frequencies in Turkish patients with dyspepsia. Methods: CYP2C19 genotype was determined in 100 Turkish patients with dyspepsia. DNA of the patients was isolated from whole blood and genotypes were detected by specific probes in real-time polymerase chain reaction (PCR). Results: The frequencies of heterozygous CYP2C19*2 and CYP2C19*3 genotypes were 13% and 1% in dyspeptic patients, respectively. Homozygous mutant CYP2C19*2 was detected at a rate of only 1% in the study population, and homozygous mutant genotype of CYP2C19*3 was not found. The frequencies of homozygous CYP2C19*2 and CYP2C19*3 genotypes were 86% and 99% in dyspeptic Turkish patients, respectively. Conclusions: This is the first study investigating CYP2C19 polymorphism in dyspeptic Turkish patients. Our investigation revealed that the most common CYP2C19 genotype was wild type CYP2C19 in dyspeptic Turkish patients. Dyspeptic Turkish patients are extensive metabolizers for proton pump inhibitors. This finding might have impact on the clinical consequences for the treatment strategies in dyspepsia.

Özet

Amaç: Dispeptik yakınmaları olan Türk hastalarda cytocrom P450 2C19 enziminin genotipik dağılımını belirlemek. Yöntem: Dispeptik yakınmaları olan 100 Türk hastada CYP2C19 genotipi belirlendi. Hastaların DNA'lı kandan ayrıldı ve genotipler real-time PCR ile spesifik problarla saptandı. Bulgular: Dispeptik hastalarda heterozigot CYP2C19*2 ve CYP2C19*3 genotipi sırasıyla %13 ve %1 saptandı. Çalışma hastalarının sadece birinde (%1) homozigot mutant CYP2C19*2 saptandı. Dispeptik hastalarda homozigot mutant CYP2C19*3 bulunmadı. Dispeptik Türk hastalarda homozigot CYP2C19*2 ve CYP2C19*3 genotipleri sırasıyla %86 ve %99 olarak bulundu. Sonuç: Bu araştırma dispeptik Türk hastalarda CYP2C19 polimorfizminin araştırıldığı ilk çalışmadır. Çalışmamız dispeptik Türk hastalarda en sık görülen CYP2C19 genotiplerinin homozigot CYP2C19*2 ve CYP2C19*3 olduğunu göstermektedir. Dispeptik Türk hastalar Proton Pompa İnhibitörleri için hızlı metabolize edicidirler. Bu bulgular dispepsi tedavisinin klinik sonuçlarında etkili olabilir.

🔖

Cite This Article

ÇELEBİ, A., KOCAMAN, O., SAVLI, H., AYGÜN, C., KONDUK, B. T., ŞENTÜRK, Ö., HÜLAGÜ, S. (2009). Dispeptik yakınmaları olan Türk hastalarda CYP2C19 mutasyonlarının prevelansı. Turkish Journal of Gastroenterology, Cilt: 20 - Sayı: 3, 161–164. https://ajindex.com/articles/409870

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Goldstein JA. Clinical relevance of genetic polymorphism in the human CYP2C subfamily. Br J Clin Pharmacol 2001; 52: 349-55
  2. Dickson EJ, Stuart RC. Genetics of response to proton pump inhibitor therapy. Am J Pharmacogenomics 2003; 3: 303-5
  3. Rosemary J, Adithan C, Padmaja N, et al. The effect of the CYP2C19 genotype on the hydroxylation index of omeprazole in South Indians. Eur J Clin Pharmacol 2005; 61: 19- 23
  4. Van Zanten SV, Thompson K. Should the presence of polymorphisms of CYP2C19 enzymes influence the choice of the proton pump inhibitor for treatment of Helicobacter pylori infection? Am J Gastroenterol 2006; 101: 1476-8
  5. Drossman DA. Rome III: the new criteria. Chin J Dig Dis 2006; 7: 181-5
  6. Chong E, Ensom M. Pharmacogenetics of the proton pump inhibitors: a systematic review. Pharmacotherapy 2003; 23: 460-71
  7. Talley NJ, Vakil N. Practice Parameters Committee of the American College of Gastroenterology. Guidelines for the management of dyspepsia. Am J Gastroenterol 2005; 100: 2324-37
  8. Lind T, Megraud F, Unge P, et al. The MACH2 study: role of omeprazole in eradication of Helicobacter pylori with 1- week triple therapies. Gastroenterology 1999; 116: 248-53
  9. Talley NJ. Therapeutic options in nonulcer dyspepsia. J Clin Gastroenterol 2001; 32: 286-93
  10. Tanum L, Malt UF. A new pharmacologic treatment of functional gastrointestinal disorder. A double-blind placebo- controlled study with Mianserin. Scand J Gastroenterol 1996; 31: 318-25
  11. Kirchheiner J, Nickchen K, Bauer M, et al. Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response. Mol Psychiatry 2004; 9: 442-73.