4.5 Article

Adiponectin and visfatin concentrations in children treated with valproic acid

期刊

EPILEPSIA
卷 49, 期 2, 页码 353-357

出版社

WILEY
DOI: 10.1111/j.1528-1167.2007.01460.x

关键词

VPA; children; weight; adiponectin; visfatin

向作者/读者索取更多资源

Chronic antiepileptic therapy with valproic acid (VPA) is associated with increased body weight and insulin resistance in adults and children. Attempts to determine the underlying pathophysiologic mechanisms have failed. Adipocytokines have recently been defined as a link between glucose and fat metabolism. We herein demonstrate that VPA-associated overweight is accompanied by lower adiponectin and higher leptin concentrations in children. The absence of any relationship with visfatin concentration does not suggest a role of this novel insulin-mimetic hormone in VPA-associated metabolic alterations. Therefore, adiponectin and leptin but not visfatin may be considered as potential regulators of glucose and fat metabolism during VPA-therapy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Editorial Material Gastroenterology & Hepatology

Highly Elevated Plasma γ-Glutamyltransferase Elevations: A Trait Caused by γ-Glutamyltransferase 1 Transmembrane Mutations

Alessandro De Grandi, Maria Franzini, Stefan Rosipal, Rastislav Rosipal, Marianna Debreova, Alessandro Corti, Elisabeth Ruetzler-Dichtl, Sabine Scholl-Buergi, Aldo Paolicchi, Alfonso Pompella, Michele Emdin, Germano Zampa, Heiko Witt, Heinz Zoller, Herbert Tilg, Ertan Mayatepek, Diran Herebian, Peter P. Pramstaller, Thomas Mueller, Andreas R. Janecke

HEPATOLOGY (2020)

Article Genetics & Heredity

Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency

Willemijn J. van Rijt, Emmalie A. Jager, Derk P. Allersma, A. Cigdem Aktuglu Zeybek, Kaustuv Bhattacharya, Francois-Guillaume Debray, Carolyn J. Ellaway, Matthias Gautschi, Michael T. Geraghty, David Gil-Ortega, Austin A. Larson, Francesca Moore, Eva Morava, Andrew A. Morris, Kimihiko Oishi, Manuel Schiff, Sabine Scholl-Buergi, Michel C. Tchan, Jerry Vockley, Peter Witters, Saskia B. Wortmann, Francjan van Spronsen, Johan L. K. Van Hove, Terry G. J. Derks

GENETICS IN MEDICINE (2020)

Article Biochemical Research Methods

Amino Acid Profiles and Compositions of Different Cultivars of Panicum miliaceum L.

Verena Wiedemair, Sabine Scholl-Buergi, Daniela Karall, Christian W. Huck

CHROMATOGRAPHIA (2020)

Article Pediatrics

Ketogenic dietary therapy: principles of implementation and application for inborn disorders of metabolism

A. Hoeller, T. Zoeggeler, B. Meisinger, U. Albrecht, D. Karall, M. Baumann, S. Scholl-Buergi

MONATSSCHRIFT KINDERHEILKUNDE (2020)

Letter Oncology

SARS-CoV-2 infection in a 7-year-old girl with pancytopenia during acute lymphocytic leukemia maintenance therapy

Benoit Bernar, Gabriele Kropshofer, Roman Crazzolara, Klaus Kapelari, Andrea Griesmacher, Thomas Mueller, Sabine Scholl-Buergi

PEDIATRIC BLOOD & CANCER (2020)

Article Genetics & Heredity

Galactokinase deficiency: lessons from the GalNet registry

M. Estela Rubio-Gozalbo, Britt Derks, Anibh Martin Das, Uta Meyer, Dorothea Moeslinger, M. Luz Couce, Aurelie Empain, Can Ficicioglu, Natalia Julia Palacios, Mariela M. De Los Santos De Pelegrin, Isabel A. Rivera, Sabine Scholl-Buergi, Annet M. Bosch, David Cassiman, Didem Demirbas, Matthias Gautschi, Ina Knerr, Philippe Labrune, Anastasia Skouma, Patrick Verloo, Saskia B. Wortmann, Eileen P. Treacy, David J. Timson, Gerard T. Berry

Summary: GALK1 deficiency can lead to neonatal elevation of transaminases, bleeding diathesis, and encephalopathy in addition to cataract. Most patients show enzyme activities <= 1% at diagnosis, with a variety of gene mutations, mainly NM_000154.1:c.82C>A (p.Pro28Thr). Thirty-five patients were diagnosed through newborn screening, which was found to be beneficial.

GENETICS IN MEDICINE (2021)

Article Physiology

Comparative Serum Analyses Identify Cytokines and Hormones Commonly Dysregulated as Well as Implicated in Promoting Osteolysis in MMP-2-Deficient Mice and Children

Hassan Sarker, Eugenio Hardy, Ayman Haimour, Mahmoud A. Karim, Sabine Scholl-Buergi, John A. Martignetti, Lorenzo D. Botto, Carlos Fernandez-Patron

FRONTIERS IN PHYSIOLOGY (2020)

Article Medicine, General & Internal

Elevated Homocysteine after Elevated Propionylcarnitine or Low Methionine in Newborn Screening Is Highly Predictive for Low Vitamin B12 and Holo-Transcobalamin Levels in Newborns

Tomaz Rozmaric, Goran Mitulovic, Vassiliki Konstantopoulou, Bernadette Goeschl, Martina Huemer, Barbara Plecko, Johannes Spenger, Saskia B. Wortmann, Sabine Scholl-Burgi, Daniela Karall, Susanne Greber-Platzer, Maximilian Zeyda

DIAGNOSTICS (2020)

Article Endocrinology & Metabolism

Method comparison of HPLC-ninhydrin-photometry and UHPLC-PITC-tandem mass spectrometry for serum amino acid analyses in patients with complex congenital heart disease and controls

Miriam Michel, Christina Salvador, Verena Wiedemair, Mark Gordian Adam, Kai Thorsten Laser, Karl-Otto Dubowy, Andreas Entenmann, Daniela Karall, Ralf Geiger, Manuela Zlamy, Sabine Scholl-Buergi

METABOLOMICS (2020)

Article Genetics & Heredity

Long-term experience with triheptanoin in 12 Austrian patients with long-chain fatty acid oxidation disorders

Thomas Zoeggeler, Katharina Stock, Monika Joerg-Streller, Johannes Spenger, Vassiliki Konstantopoulou, Miriam Hufgard-Leitner, Sabine Scholl-Buergi, Daniela Karall

Summary: Retrospective study on Austrian LC-FAOD patients showed that treatment with triheptanoin led to improvement in disease progression, reduced hospitalization days, and was well tolerated in most patients. Further prospective randomized controlled trials are needed for clarification.

ORPHANET JOURNAL OF RARE DISEASES (2021)

Article Gastroenterology & Hepatology

Increased Fecal Neopterin Parallels Gastrointestinal Symptoms in COVID-19

Felix Grabherr, Maria Effenberger, Alisa Pedrini, Lisa Mayr, Julian Schwaerzler, Simon Reider, Barbara Enrich, Gernot Fritsche, Sophie Wildner, Rosa Bellmann-Weiler, Guenter Weiss, Sabine Scholl-Buergi, Thomas Mueller, Alexander Moschen, Timon E. Adolph, Herbert Tilg

Summary: COVID-19 patients show elevated levels of fecal neopterin, especially in those experiencing gastrointestinal symptoms, indicating an inflammatory immune response in the gastrointestinal tract.

CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY (2021)

Article Immunology

Assessment of the Clinical Impact of a Liver-Specific, BCAA-Enriched Diet in Major Liver Surgery

J. Krapf, A. Schuhbeck, T. Wendel, J. Fritz, S. Scholl-Buergi, C. Boesmueller, R. Oberhuber, C. Margreiter, M. Maglione, S. Staettner, F. Messner, V Berchtold, E. Braunwarth, F. Primavesi, B. Cardini, T. Resch, D. Karall, D. Ofner, R. Margreiter, S. Schneeberger

Summary: The study aimed to investigate the impact of early postoperative nutrition on the outcome and nutrition profile of liver disease patients. The use of a BCAA-enriched diet resulted in higher patient satisfaction and compliance with nutrition, but clinical liver function tests during the 14-day study period did not show statistical differences between the BCAA group and the control group.

TRANSPLANTATION PROCEEDINGS (2021)

Article Biochemistry & Molecular Biology

ost in promiscuity? An evolutionary and biochemical evaluation of HSD10 function in cardiolipin metabolism

Yvonne Wohlfarter, Reiner Eidelpes, Ryan D. Yu, Sabrina Sailer, Jakob Koch, Daniela Karall, Sabine Scholl-Buergi, Albert Amberger, Hauke S. Hillen, Johannes Zschocke, Markus A. Keller

Summary: Multifunctional protein HSD10 has been shown to be involved in disease pathomechanisms. Recent studies have suggested that HSD10 might have phospholipase C-like activity towards cardiolipins, but experimental results have shown no physiologically relevant role of HSD10 in cardiolipid metabolism.

CELLULAR AND MOLECULAR LIFE SCIENCES (2022)

Article Genetics & Heredity

Paroxysmal and non-paroxysmal dystonia in 3 patients with biallelic ECHS1 variants: Expanding the neurological spectrum and therapeutic approaches

Sabine Illsinger, G. Christoph Korenke, Sylvia Boesch, Michael Nocker, Daniela Karall, Jean M. Nuoffer, Lucia Laugwitz, Johannes A. Mayr, Sabine Scholl-Burgi, Peter Freisinger, Tobias Kowald, Stefan Kolker, Holger Prokisch, Tobias B. Haack

EUROPEAN JOURNAL OF MEDICAL GENETICS (2020)

Article Pharmacology & Pharmacy

Targeted metabolomic analysis of serum phospholipid and acylcarnitine in the adult Fontan patient with a dominant left ventricle

Miriam Michel, Karl-Otto Dubowy, Manuela Zlamy, Daniela Karall, Mark Gordian Adam, Andreas Entenmann, Markus Andreas Keller, Jakob Koch, Irena Odri Komazec, Ralf Geiger, Christina Salvador, Christian Niederwanger, Udo Mueller, Sabine Scholl-Buergi, Kai Thorsten Laser

THERAPEUTIC ADVANCES IN CHRONIC DISEASE (2020)

暂无数据