Bilal Olcay Peker

Dr. Bilal Olcay Peker

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 October 2021 in Journal of Immunological Methods
Verified
Journal Article
Closed access
BPBilal Olcay Peker
Bilal Olcay Peker
AŞAslı Gamze Şener
Aslı Gamze Şener
FAFigen Kaptan Aydoğmuş
Figen Kaptan Aydoğmuş

8 August 2019 in Clinical Rheumatology
Verified
Journal Article
Closed access
PDF file
BPBilal Olcay Peker
Bilal Olcay Peker
AŞAslı Gamze Şener
Aslı Gamze Şener
ETEmine Figen Tarhan
Emine Figen Tarhan
SKSelçuk Kaya
Selçuk Kaya

1 December 2020 in Microbial Pathogenesis
Verified
Journal Article
Closed access
BPBilal Olcay Peker
Bilal Olcay Peker
ADAYLIN ERMAN DALOGLU
AYLIN ERMAN DALOGLU
IGIrene Görzer
Irene Görzer
EPElisabeth Puchhammer-Stöckl
Elisabeth Puchhammer-Stöckl
ÖPÖmür Mustafa Parkan
Ömür Mustafa Parkan
DÇDilek Çolak
Dilek Çolak

27 January 2021 in Mikrobiyoloji Bulteni
Verified
Journal Article
Closed access
ADAYLIN ERMAN DALOGLU
AYLIN ERMAN DALOGLU
ÖPÖmür Mustafa Parkan
Ömür Mustafa Parkan
AEAli Erdoğan
Ali Erdoğan
BPBilal Olcay Peker
Bilal Olcay Peker
RSRabia Can Sarinoglu
Rabia Can Sarinoglu
DÇDilek Çolak
Dilek Çolak
Genotype distribution of hepatitis C virus (HCV) can vary over the years between different patient groups and regions. The prevalence of intravenous drug users (IVDU) is known to increase in our country, yet there are a limited number of studies investigating the distribution of HCV genotypes in this group. These data are essential for monitorization of the changes in HCV epidemiology. The present study aimed to evaluate the five-year results of HCV genotyping among patients infected with HCV related to IVDU and unrelated to drug use. Plasma samples of 720 patients (HCV antibody, HCV RNA positive), which were sent to our laboratory for HCV genotyping between January 2014-March 2019 were analyzed. HCV RNA extraction from plasma samples was performed in the automated-extraction system of EZ1 advanced (Qiagen, Germany) using the EZ1 virus mini kit v2.0 (Qiagen, Germany). Amplicons were obtained by amplifying the 5’NCR and core gene region in the Rotorgene 6000 real-time PCR (Qiagen, Germany) device with the HCV RNA real-time quantitative 2.0 (NLM, Italy) kit. For the genotyping, a commercial line probe assay (LIPA) based on in vitro reverse hybridization GEN-C2.0 kit (NLM, Italy) which can distinguish 1, 2, 3, 4, 6 genotypes and 1a, 1b, 2a/c, 2b, 3a, 3b, 3c, 3k, 4a, 4b, 4c/d, 4e, 4f, 4h, 5a, 6a/b, 6g, 6f/q, 6m, 7a subtypes of HCV, based on variations in the 5’-NCR and core regions was used. HCV genotype distribution of 266 IVDU (93.2%: male; median age: 25 ± 6.82) and 454 non-drug users (51.3%: male; median age: 56.5 ± 16.06) were examined. In order of frequency in the group with IVDU; genotype 1a, 3a, 1b, 4c/d, 2b, 4, 3 were observed and genotype 1, 2a/c and mixed genotype (1+3a) were detected in one patient. In the group without IVDU, in order of frequency; genotype 1b, 1a, 3a, 1, 2a/c, 4 were observed and genotype 2b, 4c/d, 5a, 6a/b, 6 and mixed genotype (3+4) were detected in one patient. Genotypes 1a and 3a were significantly higher in the IVDU group (p< 0.00001, p< 0.00001), while 1b was significantly higher in patients without IVDU (p< 0.00001). Genotypes 1a and 3a were more common in young men (p< 0.00001, p= 0.000163), while 1b was higher in middleaged women (p< 0.00001). The incidence of genotypes 1b (p= 0.021) and 3a (p= 0.012) was higher in foreign nationals than the Turkish patients. When the HCV genotype distribution was examined by years, it was observed that the percentages of genotype 1b and 1a were decreasing, while the percentage of genotype 3a was increasing. As a result, in this study, HCV genotype distribution among IVDU was observed to be different from the general population without IVDU. It was found that genotypes 1a and 3a were more common in the IVDU group. As in the other regions of our country, genotype 1b was found most frequently in the general population. Genotype 3a increases significantly compared to years. In our study, the determination of genotypes existing in different parts of the world may be due to the foreign nationals living in our city and our region is a tourism center. It is also necessary to investigate whether there is an increase in IVDU over the years.

1 September 2022 in Türk Mikrobiyoloji Cemiyeti Dergisi
Verified
Journal Article
Closed access
BPBilal Olcay Peker
Bilal Olcay Peker
TMTuba Müderris
Tuba Müderris
SYSüreyya Gül Yurtsever
Süreyya Gül Yurtsever
SKSelçuk Kaya
Selçuk Kaya

12 September 2022 in Turkish Journal of Parasitology
Verified
Journal Article
Closed access
ÖBÖzlem ULUSAN BAĞCI
Özlem ULUSAN BAĞCI
FBFulya Bayındır Bilman
Fulya Bayındır Bilman
NBNurten Baran
Nurten Baran
BPBilal Olcay Peker
Bilal Olcay Peker
BPBayram Pektaş
Bayram Pektaş
SKSelçuk Kaya
Selçuk Kaya
In this study, it was aimed to retrospectively evaluate the anti-Toxoplasma IgG, IgM and avidity index results of patients who were requested for Toxoplasma serology in our hospital between 01.01.2017 and 31.12.2021. Anti-Toxoplasma antibodies are studied with Abbott Architect İ2000 SR device that using the chemiluminescent microparticle immunoassay method (CMIA), according to the company's recommendations. The age, gender, nationality, sending clinic/polyclinic, and pregnancy status information of patients were scanned from the hospital system. In the five-year period between 2017 and 2021, 29.58% of anti-Toxoplasma IgG tests requested from 12694 patients and 0.94% of anti-Toxoplasma IgM tests sent from 12546 patients were found positive. It is striking that the number of test requests is higher in women. IgG positivity is highest in women in the age group of 30-39 (9.97%), and in men in the age group of 60-69 (6.97%). IgM positivity is higher in both women and men in the 20-29 age group (0.48% and 0.38%, respectively). Anti-Toxoplasma IgG was positive in 27.78% and IgM in 0.64% of the pregnant women. IgG positivity in Turkish and Syrian pregnant women were determined as 25.88%; 47.10% and IgM positivity as 0.49% and 1.83%, respectively, and the difference was statistically significant (p<0.001). Our anti-Toxoplasma antibody positivity was found to be compatible with studies conducted in different centers in our country. The fact that IgM positivity in women is high in the 20-29 age group, which is the childbearing age, emphasizes the importance of screening before and during pregnancy. Consistent with other studies in the literature, the rate of seropositivity in Syrian pregnant women was found to be higher than Turkish. This is important in terms of showing the effect of socio-cultural behaviors on prevalence.