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©The Author(s) 2023.
World J Gastroenterol. Jan 7, 2023; 29(1): 190-199
Published online Jan 7, 2023. doi: 10.3748/wjg.v29.i1.190
Published online Jan 7, 2023. doi: 10.3748/wjg.v29.i1.190
Table 1 List of genes and primer sequences used in the study
Primer | Gene | Primer sequence | Product size (bp) |
CAGAF | CagA | 5’-GATAACAGGCAAGCTTTTGAGG-3’ | 349 |
CAGAR | 5’-CTGCAAAAGATTGTTTGGCAGA-3’ | ||
VA1-F | VacA signal region | 5’-ATGGAAATACAACAAACACAC-3’ | 259/286 (s1/s2) |
VA1-R | 5’-CTGCTTGAATGCGCCAAAC-3’ | ||
VAG-F | VacA middle region | 5’-CAATCTGTCCAATCAAGCGAG-3’ | 567/642 (m1/m2) |
VAG-R | 5’-GCGTCTAAATAATTCCAAGG-3’ |
Table 2 Demographic characteristics of the study participants, n (%)
Characteristic | Arabs, n = 56 | Jews, n = 52 | Total, n = 108 |
Sex | |||
Male | 14 (25) | 39 (23) | 26 (24) |
Female | 84 (75) | 64 (77) | 82 (76) |
Age, yr | |||
Average (range) | 40.93 (18-81) | 43.65 (18-88) | 42.30 (18-88) |
Area of residence | |||
City | 21 (37.5) | 45 (86.5) | 66 (61.1) |
Village | 35 (62.5) | 7 (13.5) | 42 (33.9) |
Table 3 The prevalence of vacuolating cytotoxin A alleles and cytotoxin-associated gene A vs patient demographics
Characteristic | CagA-positive, n = 24 | CagA-negative, n = 84 | P | VacA genotype | P | |||
s1m1 | s1m2 | s2m1 | s2m2 | |||||
Ethnicity | 0.834 | 0.729 | ||||||
Arabs | 12 (50.0) | 40 (47.6) | 11 (21.2) | 11 (21.2) | 27 (51.9) | 3 (5.8) | ||
Jewish | 12 (50.0) | 44 (52.4) | 8 (14.3) | 15 (26.8) | 31 (55.4) | 2 (3.6) | ||
Sex | 0.623 | 0.214 | ||||||
Male | 7 (29.2) | 29 (34.5) | 6 (16.7) | 5 (13.9) | 22 (61.1) | 3 (8.3) | ||
Female | 17 (70.8) | 55 (65.5) | 13 (18.1) | 21 (29.2) | 36 (50.0) | 2 (2.8) | ||
Residence | 0.149 | 0.055 | ||||||
Village | 16 (67.7) | 42 (50.0) | 8 (13.8) | 17 (29.3) | 28 (48.3) | 5 (8.6) | ||
City | 8 (33.3) | 42 (50.0) | 11 (22.0) | 9 (18.0) | 30 (60.0) | 0 (0) |
Table 4 Associations between virulence factors, patient ethnicity, and disease severity, n (%)
Disease severity | P value | |||||
Unremarkable, n = 18 | Mild, n = 50 | Moderate, n = 37 | Severe, n = 3 | Total, n = 108 | ||
Ethnicity | 0.002 | |||||
Arab | 5 (27.8) | 21 (42.0) | 28 (75.7) | 2 (66.7) | 56 (51.9) | |
Jewish | 13 (72.2) | 29 (58.0) | 9 (24.3) | 1 (33.3) | 52 (48.1) | |
Urease activity | ||||||
t1 | 0.32 (0.05) | 0.29 (0.06) | 0.29 (0.07) | 0.30 (0.06) | 0.30 (0.06) | 0.273 |
t5 | 0.32 (0.05) | 0.30 (0.05) | 0.29 (0.07) | 0.34 (0.02) | 0.30 (0.06) | 0.174 |
t10 | 0.32 (0.05) | 0.30 (0.06) | 0.30 (0.06) | 0.35 (0.04) | 0.30 (0.06) | 0.171 |
t15 | 0.33 (0.04) | 0.31 (0.05) | 0.31 (0.06) | 0.36 (0.03) | 0.31 (0.05) | 0.245 |
CagA gene | 0.534 | |||||
CagA- | 13 (72.2) | 41 (82.0) | 27 (73.0) | 3 (100) | 84 (77.8) | |
CagA+ | 5 (27.8) | 9 (18.0) | 10 (27.0) | 0 (0) | 24 (22.2) | |
VacA s allele | 0.651 | |||||
VacA s1 | 5 (27.8) | 22 (44.0) | 16 (43.2) | 1 (33.3) | 44 (40.7) | |
VacA s2 | 13 (72.2) | 28 (56.0) | 21 (56.8) | 2 (66.7) | 64 (59.3) | |
VacA m Allele | 0.652 | |||||
VacA m1 | 3 (16.7) | 14 (28.0) | 7 (18.9) | 1 (33.3) | 25 (23.1) | |
VacA m2 | 15 (83.3) | 36 (72.0) | 30 (81.1) | 2 (66.7) | 83 (76.9) | |
Genotype | 0.926 | |||||
CagA+/s1m1 | 0 (0) | 3 (6.0) | 4 (10.8) | 0 (0) | 7 (6.5) | |
CagA+/s1m2 | 1 (5.6) | 2 (4.0) | 3 (8.1) | 0 (0) | 6 (5.6) | |
CagA+/s2m2 | 2 (11.1) | 2 (4.0) | 2 (5.4) | 0 (0) | 6 (5.6) | |
CagA+/s2m1 | 1 (5.6) | 1 (2.0) | 1 (2.7) | 0 (0) | 3 (2.8) | |
CagA-/s1m1 | 2 (11.1) | 7 (14.0) | 2 (5.4) | 1 (33.3) | 12 (11.1) | |
CagA-/s1m2 | 2 (11.1) | 11 (22.0) | 7 (18.9) | 0 (0) | 20 (18.5) | |
CagA-/s2m2 | 10 (55.6) | 22 (44.0) | 18 (48.6) | 2 (66.7) | 52 (48.1) | |
CagA-/s2m1 | 0 (0) | 2 (4.0) | 0 (0) | 0 (0) | 2 (1.9) |
- Citation: Roshrosh H, Rohana H, Azrad M, Leshem T, Masaphy S, Peretz A. Impact of Helicobacter pylori virulence markers on clinical outcomes in adult populations. World J Gastroenterol 2023; 29(1): 190-199
- URL: https://www.wjgnet.com/1007-9327/full/v29/i1/190.htm
- DOI: https://dx.doi.org/10.3748/wjg.v29.i1.190