Comprehensive Research Journal of Medicine and Medical Science (CRJMMS) Vol. 2 (1) pp. 008 - 013 January, 2014 Available online http://crjournals.org/CRJMMS/Index.htm Copyright © 2014 Comprehensive Research Journals Full Length Research Paper Investigation of Hepatitis A Seropositivity in Children with Different Age Groups in Iğdır, Turkey Gülhan Arvas1, Aydoğan Bora1,Tamer Özsarı2, Bülent Kaya2, Güneş Açıkgöz3 1 Yüzüncü Yil University, Faculty of Pharmacy, Pharmaceutical Microbiology, Van, Turkey, 2 Iğdır State Hospital, Pediatric Department, Iğdır, Turkey, 3 Mustafa Kemal University, Vocational School of Health Services, Hatay, Turkey. Accepted 31 January, 2014 Aim: Hepatitis A virus (HAV) is the most common cause of hepatitis in childhood and one of the serious morbidity and mortality reason. In this study HAV values were investigated. Material and methods: In between December 2011 and January 2011 hepatitis values of 832 patients whose ages are between 1 and 15 years old were analyzed. This patients results were examined with Enzyme Linked Immunosorbend Assay (ELISA) (Vitros ECI QJ8J Company Ortho Clinical Diagnostic makro ELISA). SPSS package programe was used. The results were evaluated as statistical by chi-square test according to age groups and genders. Results: Serum samples were analyzed according to age groups and gender. Acording to gender, Immunoglobulin M antibodies to HAV (IgM anti-HAV) was found 8,4%, Immunoglobulin G antibodies to HAV (anti-HAV IgG) was found 1,9%, total anti- HAV was found 16,1%, anti-HAV IgG + anti-HAV IgM was found 0,7%, respectively. According to age groups rates were found that 32,4% from 1 to 5 ages, 58,1% from 6 to10 ages, 9,5% from 11 to 15 ages. Seroprevalence of HAV increased with ages. Conclusion: Hepatitis A is important a health problem in Iğdır province. The low level of socioeconomic development of the province and the lack of clean drinking water, inadequate infrastructure cause diseases such as hepatitis A which is transmitted through the digestive. Keywords: Hepatitis A virus; Anti-HAV IgM; Anti-HAV IgG; Total Anti-HAV INTRODUCTION Hepatitis is a general term meaning inflammation of the liver and can be caused by a variety of different viruses (WHO). Globally, there are an estimated 1.4 million cases of hepatitis A every year (WHO, Jacobsen and Koopman, 2004; WHO, 2008). *Corresponding Author E-mail: [email protected] HAV is the most common cause of hepatitis in childhood. Spread of infection is generally person to person (Cuthbert, 2001; Franco et al. 2012; Center for Disease Control and Prevention, 2006; Nainan et al., 2006) or by oral intake after fecal contamination of skin or mucous membranes; less commonly, there is fecal contamination of food or water (Cuthbert, 2001). Unfortunately, because of the long incubation period of HAV infection, virus detection in food is Gülhan et al. 009 Table I. Anti-HAV positive values according to gender Gender Anti-HAV IgM Anti-HAV IgG Anti-HAV Total Anti-HAV n(%) n(%) n(%) IgG+IgM Total n(%) Male 37 (8.1) 10 (2.2) 74 (14.0) 5 (1.1) 126 Female 33 (8.8) 6 (1.6) 60 (18.7) 1 (0.3) 100 Total 70 (8.4) 16 (1.9) 134 (16.1) 6 (0.7) 226 p=0.716 p=0.539 p=0.690 p=0.160 Table II. Anti-HAV positive values according to ages Anti-HAV IgM Anti-HAV IgG Anti-HAV Total Anti-HAV Total n(%) n(%) n(%) IgG+IgM (%) n(%) 1 to 5 ages 22(32.4) 3(18.8) 34(24.8) 2(33.3) 61(27) 6 to10 ages 41(58.1) 6(37.5) 68(51.1) 3(50) 118(52.21) 11 to 15 ages 7(9.5) 7(43.8) 32(24.1) 1(16.7) 47(20.79) Total 70 16 134 6 226 p=26.543 p=0.804 p=0.314 p=0.230 difficult, unless some of the food was kept or contamination is ongoing (Nainan et al. 2006). HAV is a small, non-enveloped RNA virus (Cuthbert, 2001; Franco et al. 2012). It is thermostable and acid-resistant (Franco et al. 2012). Usually, hepatitis A affects children without producing symptoms, but in adults it causes clinically apparent disease, often with jaundice (Koff, 1998). HAV infection rates are very low in industrialized countries (Raffaele et al., 2005). This virus is more common in low soci-oeconomic societies, crowded regions and those using untreated water (Taghavi et al. 2011). The changing epidemiology of hepatitis A virus (HAV) in many world regions heightens the need for up-to-date risk maps. Most children in low-income areas become infected in early childhood when HAV infections are typically asymptomatic, and infection confers lifelong immunity. (Hanafiah et al. 2011). Incidence of hepatitis A is highest among children 514 years of age (Center for Disease Control and Prevention; Averhoff et al. 2001). Many more children have unrecognized, asymptomatic infection and can be the source of infection for others (Center for Disease Control and Prevention, 2006). HAV infections are often acute and relief from symptoms occurs in a short time but sometimes prolonged or relapsing hepatitis is induced (Ghorbani, 2011). Until recently, immunoglobulin and improved hygiene were the only measures available to prevent and control hepatitis A (Averhoff et al. 2001). In this study ıt was aimed that to detect hepatitis A seropositivity in children between 0-15 years who applied to Igdır State Hospital. MATERIAL AND METHOD This retrospective hospital based exploratory study was conducted in the department of pediatrics, from January 2011 through December 2011 in Iğdır province. Hepatitis values of 832 children aged between 1 and 15 years with were analyzed with ELISA (Vitros ECI QJ8J Company Ortho Clinical Diagnostic makro ELISA ). The third generation of kits were used in accordance with the manufacturer's procedure. In total, 226 patients were found to HAV. SPSS 17.0 package programe was used. The results were evaluated as statistical by chi-square test according to age groups and genders. RESULTS According to the results of 832 patients, 226 patients results were found positive. Anti-HAV IgM seropositivity was detected in 70 patients (8.4%), anti-HAV IgG seropositivity was detected in 16 010 Compr. Res. J. Med. Med. Sci. Case Processing Summary(ANTI-HAV IgM) Cases Valid N hastasayısı * sonuç Missing Percent 832 N 94,4% Total Percent 49 5,6% N Percent 881 100,0% Hastasayısı * sonuç Crosstabulation sonuç hastasayısı 1-5 5-10 10-15 Total pozitif 2 Total Count 22 254 276 % within hastasayısı 8,0% 92,0% 100,0% % within sonuç 31,4% 33,3% 33,2% % of Total 2,6% 30,5% 33,2% Count 41 239 280 % within hastasayısı 14,6% 85,4% 100,0% % within sonuç 58,6% 31,4% 33,7% % of Total 4,9% 28,7% 33,7% Count 7 269 276 % within hastasayısı 2,5% 97,5% 100,0% % within sonuç 10,0% 35,3% 33,2% % of Total ,8% 32,3% 33,2% Count 70 762 832 % within hastasayısı 8,4% 91,6% 100,0% % within sonuç 100,0% 100,0% 100,0% % of Total 8,4% 91,6% 100,0% df Asymp. Sig. (2sided) 2 2 1 ,000 ,000 ,022 Chi-Square Tests Value Pearson Chi-Square Likelihood Ratio Linear-by-Linear Association N of Valid Cases 26,543 28,512 5,283 a 832 a. 0 cells (,0%) have expected count less than 5. The minimum expected count is 23,22. patients (1.9%), total anti-HAV seropositivity was detected in 134 patients (16.1%), both anti-HAV IgM and anti-HAV IgG seropositivity was detected in 6 patients (0.7%), respectively. These results in the distribution of male and female children are shown in Table I. Seventy (70) patients were evaluated according to age groups, 22 children aged 1-5 years (32.4%), 41 children aged 6-10 years (58.1%), and 7 children aged 11-15 (9.5% ) were detected anti-HAV IgM seropositivity, respectively. Sixteen (16) patients were evaluated according to age groups, 3 children aged 1-5 years (18.8%), 6 children aged 5-10 years (37.5%), 7 children aged 10-15 years (43.8%) were detected anti-HAV IgG seropositivity, respectively. One hundred and thirty four (134) patients were evaluated according to age groups, 61(27%) children aged 1-5 years, 118 (52.21%) children aged 6-10 years and 47(20.79%) children aged 11-15 were total anti-HAV seropositivity, respectively. Six (6) patients were evaluated according to age groups, 2 children aged 1-5 years (33.3%), 3 children aged 6-10 years (50%), and 1 children aged 11-15 (24.1%) were detected both anti-HAV IgM and antiHAV IgG seropositivity, respectively. Table II shows the distribution of seropositivity according to age groups. Gülhan et al. 011 Directional Measure Nominal by Nominal Lambda Value Asymp. a Error Symmetric ,048 ,035 1,332 ,183 hastasayısı Dependent ,054 ,040 1,332 ,183 sonuç Dependent Somers' d Nominal by Interval Eta c Approx. Sig. c ,016 ,005 ,000 sonuç Dependent ,032 ,011 ,000 Symmetric ,059 ,020 2,818 ,005 hastasayısı Dependent ,156 ,053 2,818 ,005 sonuç Dependent ,036 ,013 2,818 ,005 hastasayısı Dependent ,080 sonuç Dependent ,179 c. Cannot be computed because the asymptotic standard error equals zero. . b ,000 a. Not assuming the null hypothesis. b. Using the asymptotic standard error assuming the null hypothesis. d. Based on chi-square approximation Approx. T ,000 Goodman and Kruskal tau hastasayısı Dependent Ordinal by Ordinal Std. . d d 012 Compr. Res. J. Med. Med. Sci. Symmetric Measures Symmetric Measures Value Nominal by Nominal Asymp. a Error Std. Approx. T b Approx. Sig. Phi ,179 ,000 Cramer's V ,179 ,000 Contingency Coefficient ,176 Ordinal by Ordinal Gamma ,231 c Measure of Agreement Kappa . N of Valid Cases 832 ,000 ,005 ,078 2,818 a. Not assuming the null hypothesis. a. Not assuming the null hypothesis. b. Using the asymptotic standard error assuming the null hypothesis. c. Kappa statistics cannot be computed. They require a symmetric 2-way table in which the values of the first variable match the values of the second variable. DISCUSSION AND CONCLUSION Hepatitis A is the most common type of viral hepatitis infections (Cuthbert, 2001; Franco et al. 2012). It can cause debilitating symptoms and fulminant hepatitis (acute liver failure), which is associated with high mortality (Koff, 1998). A positive IgM anti-HAV indicates that infection has taken place within the past 3 to 6 months (Center for Disease Control and Prevention, 2006; Nainan et al. 2006; Minuk et al. 2005). Shortly after the appearance of the IgM anti-HAV, IgG anti-HAV appears in the circulation. IgG antibodies to HAV (IgG anti-HAV) appear soon after IgM, persist for years after infection (Nainan et al. 2006; Minuk et al. 2005). Anti-HAV seroprevalence may vary significantly between countries and regions with age. In countries, socioeconomic status, urbanization level, ethnic origin, regional hygienic standards, access to clean water and sanitation facilities may vary (Center for Disease Control and Prevention, 2006; Nainan et al. 2006; Jacobsen and Koopman, 2004). The prevalence of anti-HAV increases gradually with age (Franco et al. 2012). In this study the most patient numbers were found in the range from 6 to 10 years. The present cross-sectional study reports the burden of viral hepatitis in a population of one geographically defined area of Igdır, Turkey and potential associations with basic socio-demographic characteristics such as gender and age. There are a lot of study similarity with our study in our country. Tekay, didn’t determine any anti-HAV IgM seropositivity of children aged 0-14 years, but he detected that anti-HAV IgG+IgM seropositivity was 5.04%, anti-HAV IgG seropositivity was 62.98%, total anti-HAV seropositivity was 68.2% in his study in Hakkari, Turkey (Tekay, 2006). In our study anti-HAV IgM was determined 8.4%, anti-HAV IgG + IgM was determined 0.7%, anti-HAV IgG was determined 1.9% and anti-HAV total was determined 16.1%. Arvas et al. studied with 990 children in Igdır in their another study and they determined that anti-HAV IgM seropositivity was 18.1% in 2010 (Arvas et al. 2011). In this study, anti-HAV IgM was found 8.4%. Ceylan et al. found that children aged 0-15 years anti-HAV seropositivity was 35.5% in Istanbul, Turkey (Ceylan et al. 1997). Şahin et al. found that children aged 1–16 years anti-HAV seropositivity was 79.33% in Gaziantep, Turkey (Şahin and Aydın, 2005). In this study, male and female childrens’ results were close to each other. Based on these data, our findings suggest that the incidence of acute hepatitis was lower than other studies in the region. However, If we compare with other studies done in our country, total anti-HAV and anti-HAV IgG seropositivity is found low. Anti-HAV seroprevalence rates in the Middle East are high. More than half of Turkish children have IgG antibodies in their late teenage years (Jacobsen and Koopman, 2004). Three epidemiological patterns of HAV endemicity are commonly observed worldwide: low, intermediate and high (WHO). Turkey is a developing country and is considered an intermediate endemic region for HAV (Dinç et al. 2012). Hepatitis A is important a health problem in Iğdır province. The low level of socio-economic development and the lack of clean drinking water, inadequate infrastructure cause diseases such as hepatitis A. The endemicity of HAV infection varies according to regional hygienic standards (Nainan et al. 2006). Most studies around the world, report that the HAV epidemiologic pattern is declining in seropositivity especially in the lower age (Center for Disease Control and Prevention, 2006; 20) groups. The Gülhan et al. 013 statement about the change of epidemiologic pattern of HAV (Hanafiah et al. 2011; Center for Disease Control and Prevention, 2006; Nainan et al. 2006; Minuk et al. 2005) is feasible by comparing the seroepidemiology of HAV at two different time points in the same region (Ardakani et al. 2013). The spread of hepatitis A can be reduced, such as adequate supplies of safe drinking water, proper disposal of sewage within communities, personal hygiene practices such as regular hand-washing with safe water (WHO- Center for Disease Control and Prevention, 2006; Averhoff et al., 2001 - WHO., 2008). In addition to low-income (Hanafiah et al.,2011) households may have limited access to clean water sources, which increases risk of HAV (Jacobsen and Koopman 2004). Improvements in the hygiene of food and water have caused the displacement of HAV infections from children to adult populations which has increased the mortality rate (Hanafiah et al. 2011; Nainan et al. 2006). The national vaccination program for hepatitis A was entered to national vaccination program for September 2011 in children at Turkey. But all children between their first and second birthdays (12 through 23 months of age) should be routinely vaccinated with hepatitis A vaccine, and the other children were not made vaccination for 2011. Children and adolescents 2 through 18 years of age who live in states or communities where routine vaccination has been implemented because of high disease incidence. It is important issue for Igdır, Turkey. It is suggested that necessary precautions should be taken in order to prevent sewage water intermingling with drinking water during the time of vaccination for pre-school children and seasons of frequent rainfall. In addition to the necessary training should be given to Igdır people about this infection. REFERENCES Ardakani AT, Soltani B, Sehat M, Namjoo S, Haji Rezaei M (2013). Seroprevalence of Anti-Hepatitis A Antibody Among 1 - 15 Year Old Children in Kashan-Iran. Hepat Mons 13 (5):e10553. Arvas G, Kaya B, Berktaş M. (2011). Iğdır Devlet Hastanesine Başvuran 0-18 Yaş Grubu Çocuklarda Akut Hepatit A Seroprevalansı. Çocuk Enf. Derg.5 (4): 129-31. Averhoff F, Shapiro CN, Bell BP, Hyams I, Burd L, Deladisma A (2001). Control of hepatitis A through routine vaccination of children. JAMA 286:2968–2973. Center for Disease Control and Prevention (2006). Prevention of Hepatitis A Through Active or Passive Immunization: Recommendations of the Advisory Committee on Immunization Practices (ACIP). Accessed at:15 August 2013 Available from: http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5507a1.htm Ceylan T, Özgüneş N, Ceylan N, Üçışık AC (1997). 0–15 yaş grubu çocuklarda hepatit A ve hepatit B seroprevalansı. Viral Hepatit Dergisi 3 (2): 115-117. Cuthbert JA (2001). Hepatitis A: old and new. Clin Microbiol Rev. January; 14(1): 38–58. Dinç B, Koyuncu D, Karatayli SC, Berk E, Karatayli E, Parlak M (2012). Molecular characterization of hepatitis A virus isolated from acute infections in Turkey. Turk J Gastroenterol 23(6):7149. Franco E, Meleleo C, Serino L, Sorbara D and Zaratti L (2012). Hepatitis A: Epidemiology and prevention in developing countries. World J Hepatol 27; 4 (3): 68–73. Ghorbani GA (2011). Is Evaluation of Hepatitis A Immunity Required or Not? Hepat Mon 11(12): 955-7. Hanafiah KM, Jacobsen KH, Steven TW (2011). Challenges to mapping the health risk of hepatitis A virus infection. Int J Health Geogr 10: 57. Jacobsen KH and Koopman JS (2004). Declining hepatitis A seroprevalence: a global review and analysis. Epidemiol Infec 132: 1005–1022. Koff RS (1998). Hepatitis A. Lancet 351: 1643-1649. Minuk GY, Cohen AJ, Assy N, and Mose Mr. (2005). Viral hepatitis and the surgeon. HPB (Oxford) 7 (1): 56–64. Nainan OV, Xia G, Vaughan G and Margolis HS (2006). Clin Microbiol Rev 19 (1): 63. Nainan OV, Xia G, Vaughan G and Margolis HS (2006). Diagnosis of Hepatitis A Virus Infection: Molecular Approach. Clin Microbiol Rev 19 (1): 63. Raffaele D'A, Alfonso M, Mariano A, Romanò L, Roberto B, Florigio L, Alessandro Z, Tommaso S. (2005). Hepatitis A. Italy Emerg Infect Dis 11(7): 1155–1156. Şahin Y, Aydın D (2005). Gaziantep’te yaşayan çocuklarda hepatit A virüsü seroprevalansı. Sendrom Dergisi 17 (7): 70–72. Taghavi SA, Hosseini Asl MK, Talebzadeh M, Eshraghian A (2011). Seroprevalence study of hepatitis A virus in Fars province, southern Iran. Hepat Mon 11 (4): 285-88. Tekay F (2006). Hakkâri Devlet Hastanesine Başvuran 0–14 Yaş Grubu Çocuklarda Hepatit A Sıklığı. Dicle Tıp Dergisi.33 (4): 245-247. WHO (2008). Hepatitis A. Available at: http://www.who.int/mediacentre/factsheets/fs328/en/ WHO. Hepatitis. Available: http://www.who.int/csr/disease/hepatitis/en/index.html Accessed: at 15 August 2013.
© Copyright 2024 ExpyDoc