Abstract
Objectives
Because patients with type 1 diabetes mellitus (T1DM) have persistent and profound limitations in immune functions, immune response to vaccines may diminish. The aim of our study was to compare the antibody to Hepatitis B surface antigen (anti-HBs) serologies of children with T1DM, at the time of T1DM diagnosis, who were vaccinated according to the vaccination schedule with the anti-HBs serologies of healthy children. And to investigate the relationship between anti-HBs levels and the accompanying variables of these patients.
Methods
Anti-HBs and Hepatitis B surface antigen (HBs Ag) results of 214 children with T1DM and 210 healthy children were recorded retrospectively. Seropositivity rates for anti-HBs were compared between T1DM and control groups and the odds of seropositivity were examined. Clinical and laboratory data of T1DM patients were investigated according to anti-HBs seropositivity.
Results
Anti-HBs seropositivity rates and titers in the T1DM group were significantly lower than those in the healthy group. According to anti-HBs status among T1DM patients; no difference was found in terms of gender, BMI, presence of comorbidities, presence of autoantibodies and lipid profiles. Diagnosis age and HbA1c levels of anti-HBs negative group were higher than anti-HBs positive group in patients diagnosed with T1DM. However, neither age nor HbA1c level was found to significantly change the odds of the seropositivity for anti-HBs in T1DM patients after adjustment.
Conclusions
We recommend that children diagnosed with T1DM should have anti-HBs serology tested at the time of diagnosis and seronegative patients should have additional hepatitis B vaccination.
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Research ethics: The study was conducted in accordance with the guidelines of the Declaration of Helsinki and was approved by the Ethics Committee of the Prof Dr Cemil Tascioglu City Hospital (06.03.2024 dated, E-48670771-514.99-238484061 numbered).
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Informed consent: Not applicable.
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Author contributions: Pınar Yılmazbaş and Diğdem Bezen conceived of or designed study. Diğdem Bezen and Pınar Yılmazbaş performed research. Eren Vurgun analyzed data. Eren Vurgun, Diğdem Bezen and Pınar Yılmazbaş contributed new methods or models. Pınar Yılmazbaş wrote the paper. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: Not applicable.
References
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Articles in the same Issue
- Frontmatter
- Original Articles
- Diabetes distress, depression, and future glycemic control among adolescents with type 1 diabetes
- Is oxytocin related to psychiatric symptoms in adolescents with obesity?
- Associations between body mass index and sleep duration in Brazilian children and adolescents: the moderating role of screen time
- The transfer of care experience in young adults with type 1 diabetes
- Assessing the efficacy of a hybrid closed loop system in a racial-ethnic minority cohort of children and adolescents with type 1 diabetes
- Do children with type 1 diabetes mellitus remain protected against hepatitis B?
- Influence of excess weight on metabolic risk factors in Argentinian preschool children
- Causal associations between childhood obesity and delayed puberty or height: a bidirectional two-sample Mendelian randomization study
- Differentiating true precocious puberty and puberty variants in consecutive 275 girls: a single center experience
- Development of bone mineral density and content in children with cerebral palsy: a retrospective, longitudinal study
- Insights in non-CAH pediatric primary adrenal insufficiency: a single-center experience from India
- Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye
- Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort
- Short Communication
- The impact of the COVID-19 pandemic on DKA severity in Black and White pediatric patients
- Case Reports
- Evinacumab as an adjunct to lipid apheresis in an infant with homozygous familial hypercholesterolemia
- DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report
- Moebius syndrome and hypopituitarism: a case of multiple pituitary hormone deficiency and revision of the literature
Articles in the same Issue
- Frontmatter
- Original Articles
- Diabetes distress, depression, and future glycemic control among adolescents with type 1 diabetes
- Is oxytocin related to psychiatric symptoms in adolescents with obesity?
- Associations between body mass index and sleep duration in Brazilian children and adolescents: the moderating role of screen time
- The transfer of care experience in young adults with type 1 diabetes
- Assessing the efficacy of a hybrid closed loop system in a racial-ethnic minority cohort of children and adolescents with type 1 diabetes
- Do children with type 1 diabetes mellitus remain protected against hepatitis B?
- Influence of excess weight on metabolic risk factors in Argentinian preschool children
- Causal associations between childhood obesity and delayed puberty or height: a bidirectional two-sample Mendelian randomization study
- Differentiating true precocious puberty and puberty variants in consecutive 275 girls: a single center experience
- Development of bone mineral density and content in children with cerebral palsy: a retrospective, longitudinal study
- Insights in non-CAH pediatric primary adrenal insufficiency: a single-center experience from India
- Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye
- Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort
- Short Communication
- The impact of the COVID-19 pandemic on DKA severity in Black and White pediatric patients
- Case Reports
- Evinacumab as an adjunct to lipid apheresis in an infant with homozygous familial hypercholesterolemia
- DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report
- Moebius syndrome and hypopituitarism: a case of multiple pituitary hormone deficiency and revision of the literature