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Reciprocal impact of host factors and Helicobacter pylori genotypes on gastric diseases 被引量:5

Reciprocal impact of host factors and Helicobacter pylori genotypes on gastric diseases
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摘要 AIM: To assess the impact of Helicobacter pylori(H. pylori) genotypes and patient age and sex on the development of gastric diseases.METHODS: H. pylori-infected patients(n = 233) referred to the endoscopy unit at Tehran University of Medical Sciences(Tehran,Iran) were diagnosed with chronic gastritis(CG),gastric ulcer(GU),or duodenal ulcer(DU). Brucella blood agar was used for biopsy cultures and H. pylori isolation under microaerobic conditions. H. pylori isolates were confirmed with biochemical tests and through amplification of the 16 S r RNA gene. DNA was extracted from fresh cultures of the H. pylori isolates and used for amplification of vac A alleles and the cag A gene. Statistical analysis was performed to determine the association between H. pylori genotypes,age(< 40 years vs > 40 years) and sex of the patient,and gastric diseases.RESULTS: CG was the most prevalent gastric disease(113/233; 48.5%),compared to GU(64/233; 27.5%)and DU(56/233; 24%). More patients were male,and gastric diseases were more frequent in patients > 40 years(P < 0.05). The percentage of CG and GU patients that were male and female did not show a significant difference; however DU was more common in males(P < 0.05). Interestingly,a diagnosis of CG in patients > 40 years was more common in females(18.5%) than males(11.6%)(P = 0.05),whereas a diagnosis of GU or DU in patients > 40 years was more frequent in males(14.6% vs 10.7% and 12.4% vs 4.3%,respectively). Overall,genotyping of the H. pylori isolates revealed that the vac A s1(82%),vac A m2(70%),and cag A+(72.5%) alleles were more frequent than vac A s2(18%),vac A m1(29.2%),and cag A-(all P < 0.05). The vac A s1m2 cag A+ genotype was the most prevalent within the three disease groups. vac A s1m2 frequency was 56.2% with a similar occurrence in all diagnoses,while vac A s1m1 appeared more often in DU patients(33.9%). A genotype of vac A s2m2 occurred in 15% of isolates and was more common in CG patients(21.2%); vac A s2m1 was the least common genotype(3%). The vac A s1 allele was found to be a risk factor for DU,vac A s2 for CG,and vac A s1 and vac A s2 for GU(all P < 0.05). The vac A s2m2 genotype was associated with the development of CG and GU compared to DU(P < 0.05). No correlation was found between vac A m or cag A and gastric diseases.CONCLUSION: The outcome of H. pylori infection is the result of interaction between bacterial genotypes and the age and sex of infected individuals. AIM: To assess the impact of Helicobacter pylori(H. pylori) genotypes and patient age and sex on the development of gastric diseases.METHODS: H. pylori-infected patients(n = 233) referred to the endoscopy unit at Tehran University of Medical Sciences(Tehran,Iran) were diagnosed with chronic gastritis(CG),gastric ulcer(GU),or duodenal ulcer(DU). Brucella blood agar was used for biopsy cultures and H. pylori isolation under microaerobic conditions. H. pylori isolates were confirmed with biochemical tests and through amplification of the 16 S r RNA gene. DNA was extracted from fresh cultures of the H. pylori isolates and used for amplification of vac A alleles and the cag A gene. Statistical analysis was performed to determine the association between H. pylori genotypes,age(< 40 years vs > 40 years) and sex of the patient,and gastric diseases.RESULTS: CG was the most prevalent gastric disease(113/233; 48.5%),compared to GU(64/233; 27.5%)and DU(56/233; 24%). More patients were male,and gastric diseases were more frequent in patients > 40 years(P < 0.05). The percentage of CG and GU patients that were male and female did not show a significant difference; however DU was more common in males(P < 0.05). Interestingly,a diagnosis of CG in patients > 40 years was more common in females(18.5%) than males(11.6%)(P = 0.05),whereas a diagnosis of GU or DU in patients > 40 years was more frequent in males(14.6% vs 10.7% and 12.4% vs 4.3%,respectively). Overall,genotyping of the H. pylori isolates revealed that the vac A s1(82%),vac A m2(70%),and cag A+(72.5%) alleles were more frequent than vac A s2(18%),vac A m1(29.2%),and cag A-(all P < 0.05). The vac A s1m2 cag A+ genotype was the most prevalent within the three disease groups. vac A s1m2 frequency was 56.2% with a similar occurrence in all diagnoses,while vac A s1m1 appeared more often in DU patients(33.9%). A genotype of vac A s2m2 occurred in 15% of isolates and was more common in CG patients(21.2%); vac A s2m1 was the least common genotype(3%). The vac A s1 allele was found to be a risk factor for DU,vac A s2 for CG,and vac A s1 and vac A s2 for GU(all P < 0.05). The vac A s2m2 genotype was associated with the development of CG and GU compared to DU(P < 0.05). No correlation was found between vac A m or cag A and gastric diseases.CONCLUSION: The outcome of H. pylori infection is the result of interaction between bacterial genotypes and the age and sex of infected individuals.
出处 《World Journal of Gastroenterology》 SCIE CAS 2015年第31期9317-9327,共11页 世界胃肠病学杂志(英文版)
基金 Supported by Research Council of the University of Tehran
关键词 Age GASTRIC disease GENDER GENOTYPE HELICOBACTER p Age Gastric disease Gender Genotype Helicobacter p
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  • 1Douglas Mapel,Melissa Roberts,Andrew Overhiser,Andrew Mason.The Epidemiology, Diagnosis, and Cost of Dyspepsia and H elicobater pylori Gastritis: A Case–Control Analysis in the S outhwestern U nited S tates[J]. Helicobacter . 2012 (1)
  • 2Osamu Matsunari,Seiji Shiota,Rumiko Suzuki,Masahide Watada,Nagisa Kinjo,Kazunari Murakami,Toshio Fujioka,Fukunori Kinjo,Yoshio Yamaoka.Association between Helicobacter pylori Virulence Factors and Gastroduodenal Diseases in Okinawa, Japan[J]. Journal of Clinical Microbiology . 2012 (7)
  • 3Sreenivasan Sasidharan,Subramanion Jo Thy Lachumy,Manickam Ravichandran,Lachimanan Yoga Latha,Surasa Rao Surya Gegu.Epidemiology of Helicobacter pylori among multiracial community in Northern Peninsular,Malaysia:effect of age across race and gender[J].Asian Pacific Journal of Tropical Medicine,2011,4(1):72-75. 被引量:11
  • 4André M.N.Fialho,Andréa B.C.Braga,Manuel B.Braga Neto,Jéssica G.Carneiro,Andreia M.C.Rocha,Maria N.Rodrigues,Dulciene M.M.Queiroz,Lúcia L.B.C.Braga.Younger Siblings Play a Major Role in Helicobacter pylori Transmission Among Children From a Low‐Income Community in the Northeast of Brazil[J]. Helicobacter . 2010 (6)
  • 5ShigemiNakajima,YorihiroNishiyama,MiyokoYamaoka,TakashiYasuoka,EisaiCho.Changes in the prevalence of Helicobacter pylori infection and gastrointestinal diseases in the past 17?years[J]. Journal of Gastroenterology and Hepatology . 2010
  • 6C. Dube ,,T.C. Nkosi ,,A.M. Clarke ,,N. Mkwetshana ,,E. Green ,,R.N. Ndip ,.Helicobacter pylori Antigenemia in an Asymptomatic Population of Eastern Cape Province, South Africa: Public Health Implications[J]. Reviews on Environmental Health . 2009 (3)
  • 7Timothy L. Cover,Martin J. Blaser.Helicobacter pylori in Health and Disease[J].Gastroenterology.2009(6)
  • 8Daniela Basso,Carlo–Federico Zambon,Darren P. Letley,Alessia Stranges,Alberto Marchet,Joanne L. Rhead,Stefania Schiavon,Graziella Guariso,Marco Ceroti,Donato Nitti,Massimo Rugge,Mario Plebani,John C. Atherton.Clinical Relevance of Helicobacter pylori cagA and vacA Gene Polymorphisms[J]. Gastroenterology . 2008 (1)
  • 9Manuel R. Amieva,Emad M. El–Omar.Host-Bacterial Interactions in Helicobacter pylori Infection[J].Gastroenterology.2008(1)
  • 10D.G.Marshall,D.C.Coleman,D.J.Sullivan,H.Xia,C.A.O’Moráin,C.J.Smyth.Genomic DNA fingerprinting of clinical isolates of Helicobacter pylori using short oligonucleotide probes containing repetitive sequences[J]. Journal of Applied Microbiology . 2008 (5)

二级参考文献24

  • 1Kang JY,Wee A,Math MV,Guan R,Tay HH,Yap I,Sutherland IH.Helicobacter pylori and gastritis in patients with peptic ulcer and non-ulcer dyspepsia:ethnic differences in Singapore. Gut . 1990
  • 2nniina Salomaa-Rasanen,Timo U Kosunen et al.A "Screen-and Treat" Approach for Helicobacter pylori infection:A population-Based study in Vammala Finland. Helicobacter . 2010
  • 3Raj SM,Yap K,Haq JA,et al.Further evidence for an exceptionally lowprevalence of Helicobacter pylori infect among peptic ulcer patients innorth-eastern peninsular Malaysia. Transactions of the Royal Society of Tropical Medicine and Hygiene . 2001
  • 4Kusters JG,van Vliet AH,Kuipers EJ.Pathogenesis of Helicobacter pylori infection. Clinical Microbiology Reviews . 2006
  • 5Raymond J,,Bergeret M,Kalach N.Helicobacter pylori infection in children. Presse Medicale . 2008
  • 6Dattoli VC,Veiga RV,da Cunha SS,et al.Seroprevalence and potential risk factors for Helicobacter pylori infection in Brazilian children. Helicobacter . 2010
  • 7Farrell S,Doherty GM,Milliken I, et al.Risk factors for Helicobacter pylori infection in children:an examination of the role played by intrafamilial bed sharing. Pediatric Infectious Disease . 2005
  • 8Brown LM,Thomas TL,Ma JL,et al.Helicobacter pylori infection in rural China: exposure to domestic animals during childhood and adulthood. Scandinavian Journal of Infectious Diseases . 2001
  • 9Wu ML,,Lewin KJ.Understanding Helicobacter pylori. Human Pathology . 2001
  • 10Kaur G,Naing NN.Prevalence and ethnic distribution of Helicobacter pylori infection among endoscoped patients in North Eastern Peninsular Malaysia. Mal J Med Sci . 2003

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  • 1房静远,刘文忠,李兆申,杜亦奇,纪小龙,戈之铮,李延青,姒健敏,吕农华,吴开春,陈萦,萧树东.中国慢性胃炎共识意见(2012年,上海)[J].中国医学前沿杂志(电子版),2013,5(7):44-55. 被引量:153
  • 2MALFERTHEINER P, MEGRAUD F, O'MORAIN C, et 01. Current concepts in the management of Helicobacter pylori infection: the Maastricbt Ill Consensus Report[J]. Gut, 2007, 56(6) : 772-781.
  • 3BIERNAT MM, PONIEWIERKA E, BLASZCZUK J, et 01. Antimicrobial susceptibility of Helicobacter pylori isolates from Lower Silesia, Poland[J]. Arch Med Sci 2014, 10(3): 505-509.
  • 4FOCK KM, KATELARIS P, SUGANO K, et 01. Second Asia- Pacific consensus guidelines for Helicobacter pylori infection[J]. J Gastroenterology Hepatol, 2009, 24(10): 1587-1600.
  • 5PERRI F, FESTA V, CLIMENTE R, et ol. Rifabutin- based 'rescue therapy' for Helicobacter pylori infected patients after failure of standard regimens[J] Aliment Pharmacol Ther, 2000, 14: 311-316.
  • 6PERRI F, FESTA V, CLEMENTE R, et al. Randomized study of two"rescue"therapies for Helieobaeler pylori--infected patients after failure of standard triple therapies[J]. Am J Gastmentrol, 2001, 96(1): 58-62.
  • 7FINORINI G, VAKIL N, ZULLO A, et ol. Culture- based selection therapy for patients who did not respond to previous treatment for Helicobacter pylori infection[J]. Clin Gastroenterol Hepatol, 2013, 11(5): 507-510.
  • 8MIEHLKE S, HANSKY K, SCHNEIDER-BRACHERT W, et a/. Randomized trial of rifabutin-based triple therapy and high- dose dual therapy for rescue treatment of Helicobacter pylori resistant to both metronidazole and clarithromycin[J]. Aliment Pharmacol Ther, 2006, 24(2): 395-403.
  • 9MIEHLKE S, SCHNEIDER-BRACHERT W, KIRSCH C, et ol. One- week once- daily triple therapy with esomeprazole, moxifloxacin, and rifabutin for eradication of persistenthelico- baeter pylori resistant to both metronidazole and Clarithromycin [J]. Helicobaeter, 2008, 13: 69-74.
  • 10GISBERT JP, GISBERT JL, MARCOS S, et al. Third-line rescue therapy with levofloxacin is more effective than rifabutin rescue regimen after two Helicobacter pylori treatment failures[J]. Aliment Pharmaeol Ther, 2006, 24(10): 1469-1474.

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