| Abstract|| |
Background/Aim: Helicobacter pylori is a Gram-negative bacteria, which is associated with development of gastroduodenal diseases. The prevalence of H. pylori and the virulence markers cytotoxin-associated gene A and E (cagA, cagE) and vacuolating-associated cytotoxin gene (vacA) alleles varies in different parts of the world. H. pylori virulence markers cagA, cagE, and vacA alleles in local and Afghan nationals with H. pylori-associated gastroduodenal diseases were studied. Patients and Methods: Two hundred and ten patients with upper gastrointestinal symptoms and positive for H. pylori by the urease test and histology were included. One hundred and nineteen were local nationals and 91 were Afghans. The cagA, cagE, and vacA allelic status was determined by polymerase chain reaction. Results: The nonulcer dyspepsia (NUD) was common in the Afghan patients (P = 0.025). In Afghan H. pylori strains, cagA was positive in 14 (82%) with gastric carcinoma (GC) compared with 29 (45%) with NUD (P = 0.006), whereas cagE was positive in 11 (65%) with GC and 4 (67%) with duodenal ulcer (DU) compared with 12 (18%) with NUD (P < 0.001 and 0.021, respectively). The vacA s1a/b1was positive in 10 (59%) of GC compared with 20 (31%) in NUD (P = 0.033). In Pakistani strains, cagE was positive in 12 (60%) with GC, 7 (58%) with GU, 12 (60%) with DU compared with 11 (16%) with NUD (P < 0.001, 0.004, and < 0.001, respectively). In Pakistani strains, cagA/s1a/m1 was 39 (33%) compared with Afghans in 17 (19%) (P = 0.022). Moderate to severe mucosal inflammation was present in 51 (43%) Pakistani patients compared with 26 (28%) (P = 0.033) in Afghans. It was also associated with grade 1 lymphoid aggregate development in Pakistani patients 67 (56%) compared with 36 (40%) (P = 0.016) in Afghans. Conclusion: Distribution of H. pylori virulence marker cagE with DU was similar in Afghan and Pakistan H. pylori strains. Chronic active inflammation was significantly associated with Pakistani H. pylori strains.
Keywords: cagA , cagE, gastritis, gastric carcinoma, Helicobacter pylori
|How to cite this article:|
Yakoob J, Abbas Z, Jafri W, Usman MW, Jafri F, Awan S. Comparison of the virulence markers of helicobacter pylori and their associated diseases in patients from Pakistan and Afghanistan. Saudi J Gastroenterol 2013;19:211-8
|How to cite this URL:|
Yakoob J, Abbas Z, Jafri W, Usman MW, Jafri F, Awan S. Comparison of the virulence markers of helicobacter pylori and their associated diseases in patients from Pakistan and Afghanistan. Saudi J Gastroenterol [serial online] 2013 [cited 2020 Oct 25];19:211-8. Available from: https://www.saudijgastro.com/text.asp?2013/19/5/211/118123
Helicobacter pylori is a Gram-negative bacteria that inhabit the gastric mucosal lining. Adhesion of the bacteria to the gastric mucosa is a necessary prerequisite for the pathogenesis of H. pylori-related diseases. Although most patients are asymptomatic, persistent infection may cause chronic gastritis, gastric ulcer, gastric cancer, and duodenal ulcer. The prevalence varies among countries with existing evidence suggesting that the diversity in disease outcome may be ascribed to variations in infecting strains. , The virulence markers of H. pylori, such as cytotoxin-associated genes A (cagA) and E (cagE), vacuolating cytotoxin (vacA) and its alleles have been shown to be associated with its various manifestations.  H. pylori genotypes and their geographic distribution are linked to the severity of peptic ulcer disease (PUD). , The H. pylori genome is genetically diverse, as it can be seen in the cag pathogenicity island (PAI) and allelic variation within the vacA gene. , The cytotoxin-associated gene A (cagA) has been proposed as a marker for the cag PAI and is associated with more severe clinical outcomes. ,, The cag PAI genes contain a cagE gene that encodes a secretory protein that is required for the induction of interleukin-8 and for translocation and phosphorylation of CagA protein. , The cagE genotype has been associated with gastric cancer in some studies but contrary results have also been published.  Vacuolating cytotoxin A (vacA) is present in all H. pylori bacteria and has two variable parts, the signal or s-region, and the middle or m-region.  The "s" region and "m" region can be differentiated into s1a, s1b, s1c, s2 and m1a, m1b, m1c, and m2 subtypes, respectively. The different combination of s- and m-region allelic types determines the structure of the cytotoxin. Moreover, there is variability in vacA in the intermediate (i)-region.  The vacA "s10" and "m1" strains are associated with greater gastric epithelial damage than "s20" and "m2" strains.  VacA s1a/m1 strains are more pathogenic than s2/m2 strains. 
The prevalence of H. pylori is high in developing countries. Its seroprevalence in Pakistan exceeds 58% of general population and is common in asymptomatic populations.  Pakistan and Afghanistan are neighboring countries and many Afghan citizens avail health-care facilities within pakistan. Studies about the seroprevalence of H. pylori in Afghanistan population are lacking but it appears to be common in view of high incidence of infections having feco-oral route of transmission. Poor quality of water supply and breakdown of infrastructure, including sanitary conditions, may contribute to high prevalence of this bacterium. Although there are several recent studies examining the relationship between H. pylori virulence factors and clinical outcomes in Pakistan, , there is no study that has compared the virulence marker of Pakistani and Afghan H. pylori strains. The distribution of cagA, cagE, and vacA alleles in Pakistani and Afghan H. pylori strains from patients with upper gastrointestinal symptoms were compared and their association with clinical diagnosis was studied.
| Patients and Methods|| |
Two hundred and ten patients were included in the study. All the patients were reported positive for H. pylori infection by the rapid urease test and histology. They included 119 patients who were local nationals (69 males and 50 females with a mean age of 45 years) and 91 Afghan patients who recently travelled to Pakistan to seek health care (65 males and 26 females with a mean age of 43 years) [Table 1]. They attended the gastroenterology outpatient and endoscopy suite from June 2008 to June 2011. All presented with upper gastrointestinal symptoms and they were diagnosed as having nonulcer dyspepsia (NUD), gastric ulcer (GU), gastric carcinoma (GC), and duodenal ulcer (DU) [Table 1]. The GC were distributed in body in 22 patients (11%), in antrum 12 (6%), and in fundus in 3 patients (1%), respectively. They were adenocarcinomas: 24 were diffuse and 13 intestinal. The study was approved by the institutional ethics review committee. All patients gave an informed consent for endoscopy and participation in the study. None of the patients had received previous treatment for H. pylori infection, antibiotics, acid-reducing drugs, such as H2-receptor antagonists, acid pump inhibitors, nonsteroidal anti-inflammatory drugs, or bismuth compounds in the last four weeks. The clinical symptoms at the time of presentation and endoscopic findings were noted. Gastric biopsy specimens were taken from an area of inflammation in the antrum and corpus. Two biopsy specimens were removed for each of the rapid urease test, histology, and polymerase chain reaction (PCR). Specimens for histology were dispatched in formalin, whereas for PCR in 0.9% normal saline. The cagA PCR for 5΄ terminal, cagE and vacA alleles for the signal "s0" and middle "m" were analyzed.
|Table 1: Clinical details, histological changes, and Helicobacter pylori ce markers in the groups |
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The tissue specimens were used for the rapid urease test (Pronto Dry, Brignais, France) results were read in 30 min after sampling as directed by the manufacturer. The color change from yellow to pink was considered positive. 
Gastric biopsy specimens for histopathology were stained using hematoxylin and eosin (stain for the detection of H. pylori), and the degree of gastritis was scored in accordance with the Sydney system.  The bacterial density was graded from 0 to 3 (0, absent; 1-3, from few and isolated bacteria to colonies). The infiltration of gastric mucosa by mononuclear cells and polymorphonuclear leukocytes, atrophy, and intestinal metaplasia (IM) were graded as follows: 0, none; 1, mild; 2, moderate; 3, marked. Chronic inflammation was defined according to an increase in lymphocytes and plasma cells in the lamina propria graded into mild, moderate, or marked increase in density. Chronic active gastritis indicated chronic inflammation with neutrophilic polymorph infiltration of the lamina propria, pits, or surface epithelium graded as 0 = nil, mild ≤1/3 of pits and surface infiltrated; moderate = 1/3 to 2/3; and marked ≥2/3. Atrophy was defined as the loss of inherent glandular tissue, with or without replacement by intestinal-type epithelium. Lymphoid aggregates were defined as accumulations of lymphocytes and plasma cells without a germinal center.
DNA extraction from tissues
DNA was extracted from gastric tissue as described previously.  Briefly, gastric tissue was homogenized in sterile water and centrifuged. Lysis buffer (100 mM NaCl, 10 mM Tris-HCl [pH 8.0], 25 mM ethylenediaminetetraacetic acid (EDTA), 0.5% sodium dodecyl sulfate) and 10 μL of Proteinase K (10 mg/mL) was added followed by incubation at 50°C for 20 h. DNA was extracted by phenol-chloroform extraction and ethanol precipitation. The resulting pellet was dissolved in 40 μL of Tris-HCl and EDTA containing buffer (10 mM Tris-HCl [pH 7.4] and 0.1 mM EDTA [pH 8.0]). Samples were stored at −20°C before PCR amplification. DNA content and purity was determined by measuring the absorbance at 260 and 280 nm using a spectrophotometer (Beckman DU-600, Michigan, USA).
Polymerase chain reaction
Amplification of cagA, cagE, and vacA alleles by PCR was performed in a volume of 50 μL containing 10 mM/L Tris-HCl (pH 8.3), 50 mM/L KCl, 1.5-2.5 mM/L MgCl 2 , 200 mM/L deoxynucleoside triphosphates, 2 units Taq DNA polymerase (Promega, Wisconsin, USA) and 25 pmol of both forward and reverse primers [Table 2] used before , (synthesized by MWG Automatic synthesizer, Huntsville, USA). PCR was performed in a Perkin Elmer 9700 thermal cycler. The amplification cycles for cagA and vacA alleles are given in [Table 2]. Positive and negative reagent control reactions were performed with each batch of amplifications. DNA from H. pylori strains ATCC 43504 (vacAs1a/m1, cagA positive), ATCC 51932 (vacA s2/m2, cagA negative), and ATCC 43526 (vacA s1b/m1, cagA positive) was used to define the accuracy of the cagA. After PCR, the amplified PCR products were electrophoresed in 2% agarose gels containing 0.5% Χ Tris/acetate/EDTA, stained with ethidium bromide, and visualized under a short-wavelength ultraviolet light source.
|Table 2: Oligonucleotide primers used in typing of Helicobacter pylori cagA, cagE, and vacA alleles |
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The statistical package for social science SPSS (Release 16, standard version, copyright © SPSS; 2007) was used for data analysis. The descriptive analysis was done for demographic and clinical features. Results were presented as mean ± standard deviation for quantitative variables and number (percentage) for qualitative variables. Differences in proportion were assessed by using Pearson Chi-square test, Fisher exact test, or Likelihood ratio test where appropriate. P value less than 0.05 was considered as statistically significant.
| Results|| |
The mean age and range of the Pakistani and Afghan patients were similar. There was a significant difference in the gender of Afghan patients as there were more males 65 out of 91 (71%) compared with Pakistani patients (P = 0.045) [Table 1]. There was no significant difference in the distribution of symptoms in the two groups (P = 0.704) [Table 1]. The endoscopic diagnosis of NUD was significantly more common in the Afghan patients compared with Pakistanis (P = 0.025); 27% (32/119) Pakistani patients had PUD compared with 10% (9/91) Afghan patients (P = 0.002), whereas GC was diagnosed at a similar frequency in the two groups [Table 1].
Comparison of H. pylori genotypes in groups
The distribution of cagA and cagE was similar in Afghan and Pakistani H. pylori strains [Table 1]. In Pakistani H. pylori strains, vacAm1 was positive in 78 (66%) compared with 48 (53%) in the strains in Afghans, whereas cagA/s1a/m1 was more frequently found in Pakistani H. pylori strains 39 (33%) compared with 17 (19%) (P = 0.025) in Afghan strains.
Comparison of histological changes in groups
The density of H. pylori and neutrophil infiltration on histology was similar in the two groups [Figure 1]. Grade 1 inflammation was present in 65 (72%) Afghan patients compared with 68 (57%) (P = 0.033) in Pakistani patients [Figure 2]. It was also associated with Grade 1 lymphoid aggregate in Pakistani patients 67 (56%) compared with 36 (40%) (P = 0.016) in Afghans [Figure 3].
|Figure 1: Gastric mucosa showing a number of Helicobacter pylori organisms (H and E, ×20)|
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|Figure 2: Inflammatory activity associated with Helicobacter pylori from grades 1-3 in Pakistan and Afghan patients (P = 0.033)|
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Correlation of H. pylori genotypes with diagnosis
In Afghan H. pylori strains, cagA was positive in 14 (82%) with GC compared with 29 (45%) with NUD (P = 0.006), whereas cagE was positive in 11 (65%) with GC and 4 (67%) with DU compared with 12 (18%) with NUD (P < 0.001 and 0.021, respectively). The vacA s1a/b1 allele was present in 10 (59%) of GC compared with 20 (31%) in NUD (P = 0.033). The H. pylori genotype cagA/vacAs1a/m1 was associated in 8 (47%) with GC compared with 9 (14%) in NUD (P = 0.006) [Table 3]. The H. pylori genotype cagA/vacAs1b/m1 was associated with GC in 7 (41%) compared with 7 (11%) in NUD (P = 0.007) [Figure 4] and [Table 3].
|Figure 3: Gastric mucosal lymphoid aggregate formation associated with Helicobacter pylori varying from grades 0-1 in Pakistan and Afghan patients (P = 0.016)|
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|Figure 4: Signet ring carcinoma of the gastric epithelium showing peripheral nuclei and empty cytoplasm (H and E, ×20)|
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|Table 3: Distribution of Helicobacter pylori virulence markers in associated disease groups |
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In Pakistani H. pylori strains, cagA did not achieve significant distribution as the number of patients were less in each of the three diagnosis of GU and GC and also DU (P = 0.274) [Table 3]. cagE was positive in 12 (60%) with GC, 7 (58%) with GU, 12 (60%) with DU compared with 11 (16%) with NUD (P < 0.001, 0.004, and < 0.001 respectively) [Table 3]. The vacA allele "s1a0" was positive in 18 (90%) with GC compared with 38 (57%) in NUD (P = 0.006), whereas "m1" was positive in patients with DU in 18 (90%) and 10 (83%) in GU compared with 35 (52%) in NUD (P = 0.002 and 0.045, respectively).The H. pylori vacAs1a/m1 was associated with GC in 14 (70%), 12 (60%) in DU, and 8 (67%) in GU compared with 21 (31%) in NUD (P = 0.002, 0.020, and 0.026, respectively). The H. pylori genotype cagA/vacAs1a/m1 was associated in 13 (65%) with GC compared with 16 (24%) in NUD (P = 0.001).
Correlation of histological changes with H. pylori genotypes
Marked gastritis was associated with cagA among Afghans compared with Pakistani patients [Table 4]a. CagE was associated with neutrophil infiltration in both the groups [Table 4]a. Lymphocyte aggregation was significantly associated with cagA in Pakistanis compared with Afghan patients. The distribution of vacA alleles was not different among Afghan and Pakistani H. pylori strains except that vacAs1b/m1 and cagA/s1b/m1 were significantly distributed among Afghan H. pylori strains compared with Pakistani H. pylori strains, P = 0.010 and 0.001, respectively [Table 4]b. There were two cases of chronic atrophic gastritis among Afghan patients and five among Pakistani patients, and they were equally distributed at the antrum and corpus of the stomach in the two groups. There were four cases of IM documented in Pakistani patients, whereas none was documented in Afghan patients.
| Discussion|| |
This study showed that both Afghan and Pakistani H. pylori strains were associated with NUD in majority of the patients. The density of H. pylori strains did not vary in the two groups but Pakistani H. pylori strains exceeded in their association with moderately active inflammation and lymphocyte aggregate formation compared with Afghan strains. The distribution of virulence markers cagA, cagE, and vacA alleles were similar in the Afghan and Pakistan H. pylori strains and H. pylori cagE was associated strongly with GC and DU compared with NUD, respectively. There was a difference in the vacA signal "s" and middle "m" region types between Afghan and Pakistani H. pylori strains. Among the Afghan strains, vacA genotypes s1a and m1 did not show association with peptic ulcer and GC compared with Pakistani strain. However, vacAs1b/m1 allele in Afghan H. pylori strains was associated with GC. In comparison, vacA alleles " s1a" and "m1" were significantly associated with GC and peptic ulcer, respectively, compared with NUD in Pakistan strains. H. pylori cag/s1a/m1 was significantly associated with GC in Pakistani and GU in Afghan H. pylori strains.
In an earlier study, genotypes of H. pylori isolates obtained from 15 Afghan immigrants in Iran, the cagA was positive in 60% and cagE in 53% of Afghan isolates, while the most common vacA s-region genotype was s1 in 80% and the s1/m1 was observed in 53%.  However, there was no significant association found between cagA, cagE, and vacA genotypes and clinical outcomes in Iranian and Afghan patients.  In both Afghan and Pakistani strains, all cagE-positive strains also typed positive for cagA. The limitation of this study is that small number of strains from patients with peptic ulcer and gastric cancer was evaluated, which is rather small to reveal differences. However, the study shows that Afghan H. pylori strains are not more virulent than Pakistani strains as cagA- and cagE-positive strains were equally common in both the groups (52% vs. 52% and 35% vs. 32%, respectively). There was a strong association between H. pylori virulence marker and disease in Pakistani but not in Afghan patients suggesting that other host and environmental factors may be more important in the disease process in Afghan patients.
The study of H. pylori virulence factors in populations is important, as they contribute to disease risk. According to the latest World Health Organization data published in April 2011, stomach cancer deaths in Pakistan reached 6541 or 0.51% of total deaths with the age-adjusted death rate of 6.66 per 100,000 of population, ranking Pakistan number 97 in the world.  In comparison, stomach cancer deaths in Afghanistan reached 1604 or 0.44% of total deaths with the age-adjusted death rate of 17.07 per 100,000 of population ranking Afghanistan at number 20 in the world.  The gastric cancer rate in Pakistan is high compared with that in Afghanistan. In the absence of an East Asian- (eg., China) type universally virulent strains, this gastric cancer rate in Pakistan appears to be lower than that of stomach cancer deaths in China of 3.99% and Iran 2.34%, respectively, of total deaths. , In conclusion, distribution of H. pylori virulence marker cagE with DU was similar in Pakistan and Afghan H. pylori strains. Chronic active inflammation was significant in association with Pakistani H. pylori strains.
| Acknowledgment|| |
The work was supported by research grants from Aga Khan University Research Committee SMG to JY. We are grateful to staff members at the Juma Research Laboratory, The Aga Khan University, for their assistance during this work.
| References|| |
|1.||Go MF, Graham DY. How does H. pylori cause duodenal ulcer disease: The bug, the host or both? J Gastroenterol Hepatol 1994;9:S8-12. |
|2.||Malaty HM, Engstrand L, Pedersen NL, Graham DY. Helicobacter pylori infection: Genetic and environmental influences. A study of twins. Ann Intern Med 1994;120:982-6. |
|3.||Censini S, Lange C, Xiang Z, Crabtree JE, Ghiara P, Borodovsky M, et al. cagA-pathogenicity island of H. pylori encode type I-specific and disease-associated virulence factors. Proc Natl Acad Sci USA 1996;93:14648-53. |
|4.||van Doorn LJ, Figueiredo C, Sanna R, Pena S, Midolo P, Ng EK, et al. Expanding allelic diversity of Helicobacter pylori vacA. J Clin Microbiol 1998;36:2597-603. |
|5.||Covacci A, Telford JL, Del Giudice G, Parsonnet J, Rappuoli R. Helicobacter pylori virulence and genetic geography. Science 1999;284:1328-33. |
|6.||Yamaoka Y, Kodama T, Kita M, Imanishi J, Kashima K, Graham DY. Relation between clinical presentation, Helicobacter pylori density, interleukin 1beta and production and cagA status. Gut 1999;45:804-11. |
|7.||Tummuru MK, Sharma SA, Blaser MJ. Helicobacter pylori picB, a homologue of the Bordetella pertussis toxin secretion protein, is required for induction of IL-8 in gastric epithelial cells. Mol Microbiol 1995;18:867-76. |
|8.||Odenbreit S, Püls J, Sedlmaier B, Gerland E, Fischer W, Haas R. Translocation of Helicobacter pylori CagA into gastric epithelial cells by type IV secretion. Science 2000;287:1497-500. |
|9.||Ang TL, Fock KM, Dhamodaran S, Teo EK, Tan J. Racial differences in Helicobacter pylori, serum pepsinogen and gastric cancer incidence in an urban Asian population. J Gastroenterol Hepatol 2005;20:1603-9. |
|10.||Atherton JC, Cao P, Peek RM, Tummuru MK, Blaser MJ. Mosaicism in vacuolating cytotoxin alleles of H. pylori: Association of specific vacA types with cytotoxin production and peptic ulceration. J Biol Chem 1995;270:17771-7. |
|11.||Atherton JC, Peek RM Jr, Tham KT, Cover TL, Blaser MJ. Clinical and pathological importance of heterogeneity in vacA, the vacuolating cytotoxin gene of Helicobacter pylori. Gastroenterology 1997;112:92-9. |
|12.||Jafri W, Yakoob J, Abid S, Siddiqui S, Awan S, Nizami SQ. Helicobacter pylori infection in children: Population-based age-specific prevalence and risk factors in a developing country. Acta Pediatr 2010;99:279-82. |
|13.||Yakoob J, Abid S, Abbas Z, Jafri W, Ahmad Z, Ahmed R, et al. Distribution of Helicobacter pylori virulence markers in patients with gastroduodenal diseases in Pakistan. BMC Gastroenterol 2009;9:87. |
|14.||Ahmad T, Sohail K, Rizwan M, Mukhtar M, Bilal R, Khanum A. Prevalence of Helicobacter pylori pathogenicity-associated cagA and vacA genotypes among Pakistani dyspeptic patients. FEMS Immunol Med Microbiol 2009;55:34-8. |
|15.||Morio O, Rioux-Leclercq N, Pagenault M, Corbinais S, Ramee MP, Gosselin M, et al. Prospective evaluation of a new rapid urease test (Pronto Dry) for the diagnosis of Helicobacter pylori infection. Gastroenterol Clin Biol 2004;28:569-73. |
|16.||Price AB. The Sydney System: Histological division. J Gastroenterol Hepatol 1991;6:209-22. |
|17.||Van Zwet AA, Thijs C, Kooistra-Smid AM, Schirm J, Snijder JA. Sensitivity of culture compared with that of polymerase chain reaction for detection of Helicobacter pylori from antral biopsy samples. J Clin Microbiol 1993;31:1918-20. |
|18.||Covacci A, Rappuoli R. PCR amplification of gene sequences from Helicobacter pylori strains. In: Helicobacter pylori: Techniques for clinical diagnosis and basic research. Philadelphia: W. B. Saunders; 1996. p. 94-109. |
|19.||Akopyants NS, Clifton SW, Kersulyte D, Crabtree JE, Youree BE, Reece CA, et al. Analyses of the cag pathogenicity island of Helicobacter pylori. Mol Microbiol 1998;28:37-53. |
|20.||Dabiri H, Bolfion M, Mirsalehian A, Rezadehbashi M, Jafari F, Shokrzadeh L, et al. Analysis of Helicobacter pylori genotypes in Afghani and Iranian isolates. Pol J Microbiol 2010;59:61-6. |
|21.||Available from: http://www.worldlifeexpectancy.com/afghanistan-stomach-cancer [Last accessed on 2012 Aug 08]. |
|22.||Available from: http://www.worldlifeexpectancy.com/pakistan-stomach-cancer [Last accessed on 2012 Aug 08]. |
|23.||Available from: http://www.worldlifeexpectancy.com/china-stomach-cancer [Last accessed on 2012 Aug 08]. |
|24.||Available from: http://www.worldlifeexpectancy.com/iran-stomach-cancer [Last accessed on 2012 Aug 08]. |
Department of Medicine, The Aga Khan University, Stadium Road, Karachi-4800
Source of Support: The work was supported by research grants from
Aga Khan University Research Committee SMG to JY,, Conflict of Interest: None
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4]