METHODS: A cross sectional study was carried out in the Department of Microbiology of Mymensing Medical College, Mymensingh, Bangladesh in two time points, one was from February 2013 to September2013 and another was from March to April, 2015 . A total of 3161 adult (18-45 years) male job seekers to Malaysia attending for health check up were invited to the study and out of them 2925 could be finally enrolled. A single blood sample was collected and Widal test was carried out according to kit manufacturer's instructions and interpreted using standard guidelines.
RESULTS: The significant baseline titers for Anti TO, TH, AO, AH, BO agglutinins among the participants were found to be 1:80 for each respectively. A titer of 1: 40 was observed for BH antigen Conclusion: In case of singular Widal test, base line values for normal range should be revised and set 1:80 for all the antigens (TO, TH, AO, AH, BO, BH), except BH, for which it should be 1:40. Further studies in different geological and demographic groups are required to ascertain the use of right context and cut off values for screening and diagnostic purposes.
METHODS: Blood samples of individuals with periodontitis (PD) (n=72) and periodontally healthy (PH) (n=62) donors were obtained from Malaysian Periodontal Database and Biobanking system (MPDBS). Genomic DNA samples were analyzed for three PTGS2 SNPs (rs5275, rs20417, rs689466,) and one DEFB1 SNP (rs1047031) using Taqman SNP genotyping assays. Notably, rs20417 and rs689466 were located in the promoter region while rs5275 and rs1047031 were located in the 3' untranslated region of the transcript. Association between the SNPs and PD were then analyzed using genotypic association analysis (additive, dominant and recessive models).
RESULTS: The allelic frequency for the rs689466-G was higher in PD group (35.2%) compared that in PH group (29.0%). However, the association of rs689466-G and other SNPs with PD was not statistically significant (at 95% CI). No associations were observed for genotypic associations between the PTGS2 and DEFB1 SNPs with PD susceptibility.
CONCLUSIONS: PTGS2 (rs5275, rs20417, and rs689466) and DEFB1 (rs1047031) polymorphism was not associated with PD in Malays, unlike the Chinese, Taiwanese & European population. This suggests that other causal variants might be involved in the development and progression of PD among Malays.
MATERIALS AND METHODS: We compared the LC scores of three previous years with those of the SBCE and studied the feedback of the three stakeholders: students, examiners, and simulated patients (SPs), regarding their experience with SBCE and the suitability of SBCE as an alternative for LC in future examinations.
RESULTS: The SBCE scores were higher than those of the LC. Most of the examiners and students were not in favour of SBCE replacing LC, as such. The SPs were more positive about the proposition. The comments of the three stakeholders brought out the plus and minus points of LC and SBCE, which prompted our proposals to make SBCE more practical for future examinations.
CONCLUSION: Having analysed the feedback of the stakeholders, and the positive and negative aspects of LC and SBCE, it was evident that SBCE needed improvements. We have proposed eight modifications to SBCE to make it a viable alternative for LC.