Ilkay Ergenc

Dr. Ilkay Ergenc

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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25 July 2022
Verified
Book Chapter
Closed access
PDF file
GPGorkem Polat
Gorkem Polat
IEIlkay Ergenc
Ilkay Ergenc
HKHaluk Tarik Kani
Haluk Tarik Kani
YAYesim Ozen Alahdab
Yesim Ozen Alahdab
OAOzlen Atug
Ozlen Atug
ATAlptekin Temizel
Alptekin Temizel

1 January 2023 in Hepatology Forum
Verified
Journal Article
Open access
IEIlkay Ergenc
Ilkay Ergenc
BGBusra Gozaydinoglu
Busra Gozaydinoglu
CKCaglayan Keklikkiran
Caglayan Keklikkiran
Yusuf YilmazYusuf Yilmaz
Yusuf Yilmaz
Background and Aim: This study investigated the risk of the development of primary biliary cholangitis (PBC) in individuals who were incidentally identified as having positive antimitochondrial antibodies (AMA)-M2. Materials and Methods: We retrospectively reviewed extractable nuclear antibody (ENA) panel test results to identify the incidental AMA-M2-positive patients. Patients who filled the diagnostic criteria for PBC were excluded. AMA-M2-positive patients were further evaluated by physical examination, liver biochemistry, liver ultrasonography, and transient elas-tography (TE) and were also closely followed. Results: We included 48 (n=45, 93% female) individuals with a median age of 49 (range: 20–69) years. The median follow-up duration was 27 months (range: 9–42) after the detection of AMA-M2. Thirty-three (69%) patients had concomitant autoimmune/inflammatory disorders. Twenty-eight (58%) individuals showed seropositivity for ANA, and 21 had (43%) positive AMA. Fifteen (31%) patients developed typical PBC according to the international PBC diagnostic criteria during the follow-up, and five of them (18%) had significant fibrosis (≥8.2 kPA) by TE at the time of PBC diagnosis. Conclusion: Two-thirds of the incidental AMA-M2-positive patients devel-oped typical features of PBC after a median 27-month follow-up. Our re-sults suggest that AMA-M2 patients should be closely followed up to detect the late development of PBC.

15 August 2021 in Turkish Journal of Gastroenterology
Verified
Journal Article
Closed access
HKHaluk Tarik Kani
Haluk Tarik Kani
CDCoskun Ozer Demirtas
Coskun Ozer Demirtas
CKCaglayan Keklikkiran
Caglayan Keklikkiran
IEIlkay Ergenc
Ilkay Ergenc
SMShahin Mehdiyev
Shahin Mehdiyev
Yusuf YilmazYusuf Yilmaz
Yusuf Yilmaz
Background: Metabolic syndrome (MS) is a condition that consists of several disorders, and the individual impact of these disorders on metabolic dysfunction-associated fatty liver disease (MAFLD) is still not clear in a combined diagnosis of MS. In this study, we aimed to investigate the effect of MS on advanced fibrosis in patients with MAFLD. Methods: We recruited the patients from our gastroenterology out-patient clinic who were being followed up for MAFLD. MAFLD was diagnosed with liver biopsy in all patients. The frequency of MS and other metabolic parameters were also compared between groups with advanced fibrosis and groups in which fibrosis was not as advanced. Results: In total, we enrolled 424 biopsy-proven MAFLD patients to the study. In univariate analysis, individuals with greater age, body mass index (BMI), higher aspartate transaminase (AST), MS, impaired fasting glucose, hypertension, enlarged waist circumference (WC), diabetes mellitus (DM), and women had significantly increased risk for fibrosis. In multivariate analysis, it was found that DM, greater age, higher BMI, and increased AST were seen more commonly in MAFLD patients with advanced fibrosis Conclusion: Greater age, a higher BMI, higher AST and a diagnosis of diabetes were more commonly associated with advanced fibrosis. However, DM was found to be the strongest predictive factor of advanced fibrosis in our cohort (OR: 2.495). Multivariate analyses did not indicate a significantly common occurrence of MS in the advanced fibrosis group, despite its important role in MAFLD pathophysiology.

1 January 2023 in Journal of Medical Biochemistry
Verified
Journal Article
Open access
PDF file
IEIlkay Ergenc
Ilkay Ergenc
ECEmre Capar
Emre Capar
SESengel Erturk
Sengel Erturk
GBGunel Bahramzade
Gunel Bahramzade
FAFatih Atalah
Fatih Atalah
ZOZekaver Odabasi
Zekaver Odabasi
Introduction: Lactate dehydrogenase (LDH) levels are predictive of coronavirus disease 2019 (COVID-19) severity. We investigated LDH isoenzyme levels to identify the tissue responsible for serum LDH elevation in patients with COVID-19. Materials and Methods: Hospitalised COVID-19 patients with serum LDH levels exceeding the upper limit of normal were included. LDH isoenzymes were detected quantitatively on agarose gels. The radiological severity of lung involvement on computed tomography was scored as 0–5 for each lobe (total possible score, 0–25). Disease severity was determined using the World Health Organization (WHO) clinical progression scale. Results: In total, 111 patients (mean age, 59.96 ± 16.14), including 43 females (38.7%), were enrolled. The serum levels of total LDH and all five LDH isoenzymes were significantly higher in the severe group. The levels of all LDH isoenzymes excluding LDH5 positively correlated with the WHO score. LDH3 levels correlated with chest computed tomography findings (r2 = 0.267, p = 0.005). On multivariate analysis, LDH3 was an independent risk factor for the deterioration of COVID-19. Discussion: LDH3 appears to be an independent risk factor for deterioration in patients with COVID-19. LDH elevation in patients with COVID-19 predominantly resulted from lung, liver and muscle damage.

6 February 2024 in Nutrition in Clinical Practice
Verified
Journal Article
Closed access
IEIlkay Ergenc
Ilkay Ergenc
CBChasan Ismail Basa
Chasan Ismail Basa
AUAlper Uzum
Alper Uzum
SSSevval Sahin
Sevval Sahin
HKHaluk Tarık Kani
Haluk Tarık Kani
YAYeşim Özen Alahdab
Yeşim Özen Alahdab

20 July 2024 in Heliyon
Verified
Journal Article
Open access
IEIlkay Ergenc
Ilkay Ergenc
EKErdogan Kara
Erdogan Kara
MYMuhammed Emre Yilmaz
Muhammed Emre Yilmaz
CDCoskun Ozer Demirtas
Coskun Ozer Demirtas
CKCaglayan Keklikkiran
Caglayan Keklikkiran
Yusuf YilmazYusuf Yilmaz
Yusuf Yilmaz
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a growing global epidemic in Türkiye and worldwide. The aim of this study was to evaluate the prevalence and predictors of MASLD and steatohepatitis among adults who died of unnatural causes including sudden death and non-burn trauma. We conducted a prospective review of all consecutive adult forensic autopsies for natural (sudden unexpected) and non-natural (Suicidal, homicidal and accidental) suspicious deaths carried out at the Istanbul Council of Forensic Medicine from February to May 2022. Four wedge biopsies were extracted from sagittal sectioned liver specimens. A liver pathologist with 20 years of experience examined each case for steatosis, ballooning, inflammation, and fibrosis. Among 1797 autopsies, 62 met inclusion criteria. Overall, 43.3 % (n = 26) of autopsies showed evidence of steatotic liver disease, with a distribution of steatosis severity as: Grade I (28.3 %), Grade II (6.6 %), and Grade III (8.3 %). All these cases met at least one cardiometabolic criteria and diagnosed with MASLD. Ballooning was observed in 20.0 % of cases (5 cases grades 1 and 7 cases grade 2), and Inflammation was present in 51.7 % (9 cases with grade 0-1, 12 with 1-2, 7 with 2-3, and 3 with 5-6). Notably, 46.1 % (n = 12) of MASLD cases and 20.0 % (n = 12) of all cases were diagnosed with steatohepatitis, with three cases exhibiting delicate perisinusoidal fibrosis and one case showing portal fibrosis. The histopathological findings from this autopsy study confirmed the markedly high prevalence of MASLD and steatohepatitis within the general adult population, highlighting the concerning burden of steatotic liver disease in Türkiye.