Saxena A, Prasad KN, Ghoshal UC, Bhagat MR, Krishnani N, Husain N. Polymorphism of -765G > C COX-2 is a risk factor for gastric adenocarcinoma and peptic ulcer disease in addition to H pylori infection: A study from northern India. World J Gastroenterol 2008; 14(10): 1498-1503 [PMID: 18330937 DOI: 10.3748/wjg.14.1498]
Corresponding Author of This Article
Kashi Nath Prasad, Professor, Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226014, India. knprasad@sgpgi.ac.in
Article-Type of This Article
H Pylori
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Table 3H pylori infection and COX-2 polymorphism as risk for gastric adenocarcinoma
H pylori status
COX-2 genotype
Gastric adenocarcinoma (n = 62)
Non-ulcer dyspepsia (Controls, n = 241)
OR (95% CI)
P-value
HP-
GG
8
79
Referent
HP-
C carriers
19
29
7.06 (2.61-19.09)
< 0.001
HP+
GG
6
92
0.83 (0.26-2.59)
0.747
HP+
C carriers
29
41
7.83 (3.09-19.85)
< 0.001
Table 4H pylori infection and COX-2 polymorphism as risk for peptic ulcer disease
H pylori status
COX-2 genotype
Peptic ulcer disease (n = 45)
Non-ulcer dyspepsia (Controls, n = 241)
OR (95% CI)
P-value
HP-
GG
8
79
Referent
HP-
C carriers
1
29
0.86 (0.09-7.48)
0.89
HP+
GG
23
92
2.83 (1.18-6.73)
0.019
HP+
C carriers
13
41
5.65 (2.07-15.34)
< 0.001
Table 5 C allele frequency and C carrier distribution in control populations from various countries
Country
Control
C allele
C carrier
Reference
population (n)
Frequency (%)
distribution (%)
America
USA
228
21
37
27
USA (African American)
100
32
52
27
Europe
Portugal
210
22
38
34
Italy
864
28
50
31
UK
454
14
25
22
Poland
547
17
31
30
Australia
Australia
168
17
31
32
Asia
India
241
16
29
Present study
Singapore
1177
5
9
23
Japan
241
2
5
24
China
1270
2
4
19
Citation: Saxena A, Prasad KN, Ghoshal UC, Bhagat MR, Krishnani N, Husain N. Polymorphism of -765G > C COX-2 is a risk factor for gastric adenocarcinoma and peptic ulcer disease in addition to H pylori infection: A study from northern India. World J Gastroenterol 2008; 14(10): 1498-1503