Evidence map›Paper›PMID 36326406›Full record

ArticleTurkish journal of medical sciences2022

Could lysosomal acid lipase enzyme activity be used for clinical follow-up in cryptogenic cirrhosis?

Engin Köse, Elçin Çağatay, Tutku Yaraş, Pelin Teke Kısa, Seminay Güler, Zümrüt Arslan Gülten, Mesut Akarsu, Yavuz Oktay, Hülya Ayar Kayalı, Nur Arslan

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Article in Turkish journal of medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Engin KöseDepartment of Pediatric Metabolism, Faculty of Medicine, Ankara University, Ankara, Turkey.
Elçin ÇağatayDepartment of Molecular Biology and Genetics, International Biomedicine and Genome Institute, Dokuz Eylül University, İzmir, Turkey.
Tutku YaraşDepartment of Basic and Translational Research, International Biomedicine and Genome Center, İzmir, Turkey.
Pelin Teke KısaDepartment of Pediatric Metabolism, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Seminay GülerDepartment of Gastroenterology, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Zümrüt Arslan GültenDepartment of Pediatric Metabolism, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Mesut AkarsuDepartment of Gastroenterology, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Yavuz OktayDepartment of Medical Biology, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Hülya Ayar KayalıDepartment of Science Chemistry, Dokuz Eylül University, İzmir, Turkey.
Nur ArslanDepartment of Pediatric Metabolism, Faculty of Medicine, Dokuz Eylül University, İzmir, Turkey.
Ankara University · TRDokuz Eylül University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCholesterol ester storage disease (CESD) is one of the rare causes that should be kept in mind in the etiology of cirrhosis. Recent studies detected that significantly reduced lysosomal acid lipase deficiency enzyme (LAL) in patients with cryptogenic cirrhosis (CC). Moreover, studies have evaluated that LAL activity is as effective as scoring systems in assessing the severity of cirrhosis. In this study, we aimed to investigate the CESD with LAL level and mutation analysis of LIPA gene in patients diagnosed with CC and to compare LAL activities between patients with CC and healthy volunteers.

methodsLaboratory parameters and cirrhosis stage (CHILD and MELD) were recorded for the patient group included in the study. In addition, blood samples were taken from each case included in the study for LAL activity determination and LIPA gene analysis.

resultsA statistically significant decrease in LAL activity was found in patients diagnosed with CC compared to the healthy group. LIPA gene analysis did not detect CESD in any patient group. Correlation analysis showed a positive correlation between LAL activity and white blood cell and platelet counts in both healthy volunteers and CC patient groups. In the univariate and multivariate logistic regression analysis of the parameters associated with the MELD of ≥10 in patients with CC, significant relationship was found between the MELD of ≥10 and the LAL activity. DISCUSSION: In our study, LAL activity was significantly lower in CC patients than in the normal population. LAL activity level appears to be a parameter that can be used to assess the severity of cirrhosis.

Indexed as

Sterol EsteraseWolman DiseaseFollow-Up StudiesHumansLiver CirrhosisSterol EsteraseCholesterol ester storage diseasecryptogenic cirrhosisLIPA genelysosomal acid lipase deficiency

Identifiers

PMID36326406
PMCPMC10387917
OpenAlexW4291498094

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.