LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy

Molecular Genetics and Metabolism Reports - Tập 5 - Trang 85-88 - 2015
Inge A. Meijer1, Florin Sasarman2, Catalina Maftei3, Elsa Rossignol1, Michel Vanasse1, Péter Major1, Grant A. Mitchell3, Catherine Brunel‐Guitton2,3
1Division of Pediatric Neurology, Department of Pediatrics, Université de Montréal, and CHU Sainte Justine, 3175 Côte Sainte-Catherine, Montreal, Quebec H3T 1C5, Canada
2Division of Biochemical Genetics Laboratory, Université de Montréal and CHU Sainte Justine, 3175 Côte Sainte-Catherine, Montreal, Quebec H3T 1C5, Canada
3Medical Genetics, Department of Pediatrics, Université de Montréal and CHU Sainte Justine, 3175 Côte Sainte-Catherine, Montreal, Quebec H3T 1C5, Canada

Tóm tắt

Từ khóa


Tài liệu tham khảo

Elsayed, 2010, Rhabdomyolysis: a review, with emphasis on the pediatric population, Pediatr. Nephrol., 25, 7, 10.1007/s00467-009-1223-9

Quinlivan, 2012, Myopathic causes of exercise intolerance with rhabdomyolysis, Dev. Med. Child Neurol., 54, 886, 10.1111/j.1469-8749.2012.04320.x

Michot, 2010, LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood, Hum. Mutat., 31, E1564, 10.1002/humu.21282

Zeharia, 2008, Mutations in LPIN1 cause recurrent acute myoglobinuria in childhood, Am. J. Hum. Genet., 83, 489, 10.1016/j.ajhg.2008.09.002

Pichler, 2015, A novel therapeutic approach for LPIN1 mutation-associated rhabdomyolysis–the Austrian experience, Muscle Nerve, 52, 437, 10.1002/mus.24749

Bergounioux, 2012, Fatal rhabdomyolysis in 2 children with LPIN1 mutations, J. Pediatr., 160, 1052, 10.1016/j.jpeds.2012.02.033

de Lonlay, 2013

Michot, 2012, Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia, J. Inherit. Metab. Dis., 35, 1119, 10.1007/s10545-012-9461-6

Zhang, 2014, Lipin-1 regulates autophagy clearance and intersects with statin drug effects in skeletal muscle, Cell Metab., 20, 267, 10.1016/j.cmet.2014.05.003

Donkor, 2009, A conserved serine residue is required for the phosphatidate phosphatase activity but not the transcriptional coactivator functions of lipin-1 and lipin-2, J. Biol. Chem., 284, 29968, 10.1074/jbc.M109.023663

Reue, 2009, The lipin family: mutations and metabolism, Curr. Opin. Lipidol., 20, 165, 10.1097/MOL.0b013e32832adee5

Han, 2006, The Saccharomyces cerevisiae Lipin homolog is a Mg2+-dependent phosphatidate phosphatase enzyme, J. Biol. Chem., 281, 9210, 10.1074/jbc.M600425200

Csaki, 2013, Lipins, lipinopathies, and the modulation of cellular lipid storage and signaling, Prog. Lipid Res., 52, 305, 10.1016/j.plipres.2013.04.001

Lamari, 2015, An overview of inborn errors of complex lipid biosynthesis and remodelling, J. Inherit. Metab. Dis., 38, 3, 10.1007/s10545-014-9764-x

Wortmann, 2015, Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids, J. Inherit. Metab. Dis., 38, 99, 10.1007/s10545-014-9759-7

Zhang, 2014, Troxerutin improves hepatic lipid homeostasis by restoring NAD(+)-depletion-mediated dysfunction of lipin 1 signaling in high-fat diet-treated mice, Biochem. Pharmacol., 91, 74, 10.1016/j.bcp.2014.07.002

Dwyer, 2012, Mouse lipin-1 and lipin-2 cooperate to maintain glycerolipid homeostasis in liver and aging cerebellum, Proc. Natl. Acad. Sci. U. S. A., 109, E2486, 10.1073/pnas.1205221109

Donkor, 2008, Adipose tissue lipin-1 expression is correlated with peroxisome proliferator-activated receptor alpha gene expression and insulin sensitivity in healthy young men, J. Clin. Endocrinol. Metab., 93, 233, 10.1210/jc.2007-1535

Finck, 2006, Lipin 1 is an inducible amplifier of the hepatic PGC-1alpha/PPARalpha regulatory pathway, Cell Metab., 4, 199, 10.1016/j.cmet.2006.08.005

Kim, 2013, Lipin1 regulates PPARgamma transcriptional activity, Biochem. J., 453, 49, 10.1042/BJ20121598

Michot, 2013, Combination of lipid metabolism alterations and their sensitivity to inflammatory cytokines in human lipin-1-deficient myoblasts, Biochim. Biophys. Acta, 1832, 2103, 10.1016/j.bbadis.2013.07.021

Hamel, 2015, Acute rhabdomyolysis and inflammation, J. Inherit. Metab. Dis., 38, 621, 10.1007/s10545-015-9827-7

Gardner, 2011, Chromosome abnormalities and genetic counseling, 648

Herlin, 2013, Efficacy of anti-IL-1 treatment in Majeed syndrome, Ann. Rheum. Dis., 72, 410, 10.1136/annrheumdis-2012-201818

Zhang, 2008, Regulation of lipin-1 gene expression by glucocorticoids during adipogenesis, J. Lipid Res., 49, 1519, 10.1194/jlr.M800061-JLR200