Ece Kartal

Ece Kartal

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Ece Kartal

Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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1 April 2019 in Nature Medicine
Verified
Journal Article
Closed access
PDF file
JWJakob Wirbel
Jakob Wirbel
PPPaul Theodor Pyl
Paul Theodor Pyl
EKEce Kartal
Ece Kartal
KZKonrad Zych
Konrad Zych
AKAlireza Kashani
Alireza Kashani
GZGeorg Zeller
Georg Zeller

8 March 2022 in Gut
Verified
Journal Article
Open access
PDF file
EKEce Kartal
Ece Kartal
TSThomas S B Schmidt
Thomas S B Schmidt
EMEsther Molina-Montes
Esther Molina-Montes
SRSandra Rodriguez-Perales
Sandra Rodriguez-Perales
JWJakob Wirbel
Jakob Wirbel
PBPeer Bork
Peer Bork
Background Recent evidence suggests a role for the microbiome in pancreatic ductal adenocarcinoma (PDAC) aetiology and progression. Objective To explore the faecal and salivary microbiota as potential diagnostic biomarkers. Methods We applied shotgun metagenomic and 16S rRNA amplicon sequencing to samples from a Spanish case–control study (n=136), including 57 cases, 50 controls, and 29 patients with chronic pancreatitis in the discovery phase, and from a German case–control study (n=76), in the validation phase. Results Faecal metagenomic classifiers performed much better than saliva-based classifiers and identified patients with PDAC with an accuracy of up to 0.84 area under the receiver operating characteristic curve (AUROC) based on a set of 27 microbial species, with consistent accuracy across early and late disease stages. Performance further improved to up to 0.94 AUROC when we combined our microbiome-based predictions with serum levels of carbohydrate antigen (CA) 19–9, the only current non-invasive, Food and Drug Administration approved, low specificity PDAC diagnostic biomarker. Furthermore, a microbiota-based classification model confined to PDAC-enriched species was highly disease-specific when validated against 25 publicly available metagenomic study populations for various health conditions (n=5792). Both microbiome-based models had a high prediction accuracy on a German validation population (n=76). Several faecal PDAC marker species were detectable in pancreatic tumour and non-tumour tissue using 16S rRNA sequencing and fluorescence in situ hybridisation. Conclusion Taken together, our results indicate that non-invasive, robust and specific faecal microbiota-based screening for the early detection of PDAC is feasible.

30 March 2021 in Genome Biology
Verified
Journal Article
Open access
PDF file
JWJakob Wirbel
Jakob Wirbel
KZKonrad Zych
Konrad Zych
MEMorgan Essex
Morgan Essex
NKNicolai Karcher
Nicolai Karcher
EKEce Kartal
Ece Kartal
GZGeorg Zeller
Georg Zeller
The human microbiome is increasingly mined for diagnostic and therapeutic biomarkers using machine learning (ML). However, metagenomics-specific software is scarce, and overoptimistic evaluation and limited cross-study generalization are prevailing issues. To address these, we developed SIAMCAT, a versatile R toolbox for ML-based comparative metagenomics. We demonstrate its capabilities in a meta-analysis of fecal metagenomic studies (10,803 samples). When naively transferred across studies, ML models lost accuracy and disease specificity, which could however be resolved by a novel training set augmentation strategy. This reveals some biomarkers to be disease-specific, with others shared across multiple conditions. SIAMCAT is freely available fromsiamcat.embl.de.

1 April 2015 in Neurobiology of Aging
Verified
Journal Article
Closed access
AÖAslıhan Özoğuz
Aslıhan Özoğuz
ÖUÖzgün Uyan
Özgün Uyan
GBGüneş Birdal
Güneş Birdal
CICeren Iskender
Ceren Iskender
EKEce Kartal
Ece Kartal
ABA. Nazlı Başak
A. Nazlı Başak

10 May 2019 in Advances in Nutrition
Verified
Journal Article
Closed access
PDF file
SSSolomon A Sowah
Solomon A Sowah
LRLena Riedl
Lena Riedl
ADAntje Damms-Machado
Antje Damms-Machado
TJTheron S Johnson
Theron S Johnson
RSRuth Schübel
Ruth Schübel
TKTilman Kühn
Tilman Kühn
Short-chain fatty acids (SCFAs, mainly acetate, propionate, and butyrate), which are primarily derived from the gut microbiome, may exert anti-inflammatory and immunomodulatory effects, and regulate energy homeostasis. It has been suggested that weight loss may affect SCFA metabolism, but a systematic review of intervention studies is lacking. We aimed to systematically assess the effects of dietary, physical activity–based, and surgical weight-loss interventions among overweight [body mass index (BMI) 25–29.9 kg/m2)] or obese (BMI ≥30 kg/m2) adults (≥18 y) on concentrations of acetate, propionate, butyrate, and total SCFAs in blood, urine, or feces. We conducted a systematic literature search in PubMed, Web of Science, and the Cochrane Central Register of Controlled Trials (CENTRAL) up to April 30, 2018 for randomized and nonrandomized weight-loss trials among overweight or obese adults, in which the concentrations of individual and total SCFAs were assessed. A total of 9 studies consisting of 2 randomized parallel-arm trials, 4 crossover trials, and 3 nonrandomized clinical or surgical trials were included. In the majority of studies, changes in fecal SCFA concentrations were assessed, whereas changes in serum SCFAs were reported from 1 trial. Individual and total SCFA concentrations either remained unchanged or decreased significantly following weight loss. Three of the dietary interventions that resulted in decreased SCFA concentrations were low (≤5% of energy) in total carbohydrates. Most of the studies had a high risk of bias. Decreases in SCFA concentrations may accompany weight loss induced by bariatric surgery or dietary restriction among overweight or obese adults, particularly when carbohydrate intake is reduced. However, findings were inconsistent and based on studies with high to unclear risk of bias, and small sample sizes. Because measurements of fecal SCFAs may not be ideal due to limited sample standardization, well-powered trials with repeated blood measurements of SCFAs are required. This review was registered at PROSPERO as CRD42018088716.

1 August 2016 in Parkinsonism & Related Disorders
Verified
Journal Article
Closed access
HHHasmet A. Hanagasi
Hasmet A. Hanagasi
AGAnamika Giri
Anamika Giri
EKEce Kartal
Ece Kartal
GGGamze Guven
Gamze Guven
BBBasar Bilgic
Basar Bilgic
ELEbba Lohmann
Ebba Lohmann