Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up

. 2019 Feb 22 ; 14 (1) : 55. [epub] 20190222

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid30795770
Odkazy

PubMed 30795770
PubMed Central PMC6387484
DOI 10.1186/s13023-019-1029-1
PII: 10.1186/s13023-019-1029-1
Knihovny.cz E-zdroje

BACKGROUND: Acid sphingomyelinase deficiency (ASMD), due to mutations in the sphingomyelin phosphodiesterase 1 (SMPD1) gene, is divided into infantile neurovisceral ASMD (Niemann-Pick type A), chronic neurovisceral ASMD (intermediate form, Niemann-Pick type A/B) and chronic visceral ASMD (Niemann-Pick type B). We conducted a long-term observational, single-center study including 16 patients with chronic visceral ASMD. RESULTS: 12 patients were diagnosed in childhood and 4 others in adulthood, the oldest at the age of 50. The mean time of follow-up was approximately 10 years (range: 6 months - 36 years). Splenomegaly was noted in all patients at diagnosis. Hepatomegaly was observed in 88% of patients. Moderately elevated (several-fold above the upper limit of normal values) serum transaminases were noted in 38% of patients. Cherry-red spots were found in five Gypsy children from one family and also in one adult Polish patient, a heterozygote for p.delR610 mutation. Dyslipidemia was noted in 50% of patients. Interstitial lung disease was diagnosed in 44% of patients. Plasmatic lysosphingomyelin (SPC) was elevated in all the patients except one with p.V36A homozygosity and a very mild phenotype also presenting with elevated plasmatic SPC-509 but normal chitotriosidase activity. The most common variant of SMPD1 gene was p.G166R. We found a previously unreported variant in exon 2 (c.491G > T, p.G164 V) in one patient. CONCLUSIONS: Chronic visceral ASMD could constitute a slowly progressing disease with a relatively good outcome. The combined measurement of lysosphingomyelin (SPC) and lysospingomyelin-509 (SPC-509) is an essential method for the assessment of ASMD course.

Zobrazit více v PubMed

Schuchman EH, Desnick RJ. Types a and B Niemann-pick disease. Mol Genet Metab. 2017;120:27–33. doi: 10.1016/j.ymgme.2016.12.008. PubMed DOI PMC

McGovern MM, Avetisyan R, Sanson BJ, Lidove O. Disease manifestations and burden of illness in patients with acid sphingomyelinase deficiency (ASMD) Orphanet J Rare Dis. 2017;12:41. doi: 10.1186/s13023-017-0572-x. PubMed DOI PMC

Pavlů-Pereira H, Asfaw B, Poupctová H, et al. Acid sphingomyelinase deficiency. Phenotype variability with prevalence of intermediate phenotype in a series of twenty-five Czech and Slovak patients. A multi-approach study. J Inherit Metab Dis. 2005;28:203–227. doi: 10.1007/s10545-005-5671-5. PubMed DOI

Wasserstein MP, Aron A, Brodie SE, Simonaro C, Desnick RJ, McGovern MM. Acid sphingomyelinase deficiency: prevalence and characterization of an intermediate phenotype of Niemann-pick disease. J Pediatr. 2006;149:554–559. doi: 10.1016/j.jpeds.2006.06.034. PubMed DOI

McGovern MM, Dionisi-Vici C, Giugliani R, Hwu P, Lidove O, Lukacs Z, Eugen Mengel K, Mistry PK, Schuchman EH, Wasserstein MP. Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency. Genet Med. 2017;19:967–974. doi: 10.1038/gim.2017.7. PubMed DOI PMC

McGovern MM, Wasserstein MP, Giugliani R, et al. A prospective, cross-sectional survey study of the natural history of Niemann-pick disease type B. Pediatrics. 2008;122:e341–e349. doi: 10.1542/peds.2007-3016. PubMed DOI PMC

Wasserstein MP, Desnick RJ, Schuchman EH, et al. The natural history of type B Niemann-pick disease: results from a 10-year longitudinal study. Pediatrics. 2004;114:e672–e677. doi: 10.1542/peds.2004-0887. PubMed DOI

Hollak CE, de Sonnaville ES, Cassiman D, et al. Acid sphingomyelinase (Asm) deficiency patients in the Netherlands and Belgium: disease spectrum and natural course in attenuated patients. Mol Genet Metab. 2012;107:526–533. doi: 10.1016/j.ymgme.2012.06.015. PubMed DOI

Lidove O, Belmatoug N, Froissart R, Lavigne C, Durieu I, Mazodier K, Serratrice C, Douillard C, Goizet C, Cathebras P, Besson G, Amoura Z, Tazi A, Gatfossé M, Rivière S, Sené T, Vanier MT, Ziza JM. Acid sphingomyelinase deficiency (Niemann-pick disease type B) in adulthood: a retrospective multicentric study of 28 adult cases. Rev Med Interne. 2017;38:291–299. doi: 10.1016/j.revmed.2016.10.387. PubMed DOI

Gal AE, Fash FJ. Synthesis of 2-n-(hexadecanoyl)-amino-4-nitrophenyl phosphorylcholine-hydroxide, a chromogenic substrate for assaying sphingomyelinase activity. Chem Phys Lipids 1976;161:71–79. PubMed

Hollak CE, van Weely S, van Oers MH, Aerts JM. Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease. J Clin Invest. 1994;93:1288–1292. doi: 10.1172/JCI117084. PubMed DOI PMC

Kuchar L, Sikora J, Gulinello ME, Poupetova H, Lugowska A, Malinova V, Jahnova H, Asfaw B, Ledvinova J. Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-pick a/B and C diseases. Anal Biochem. 2017;525:73–77. doi: 10.1016/j.ab.2017.02.019. PubMed DOI

Rhein C, Mühle C, Kornhuber J, Reichel M. Alleged detrimental mutations in the SMPD1 gene in patients with Niemann-pick disease. Int J Mol Sci. 2015;16:13649–13652. doi: 10.3390/ijms160613649. PubMed DOI PMC

McGovern MM, Lippa N, Bagiella E, Schuchman EH, Desnick RJ, Wasserstein MP. Morbidity and mortality in type B Niemann-pick disease. Genet Med. 2013;15:618–623. doi: 10.1038/gim.2013.4. PubMed DOI

Cassiman D, Packman S, Bembi B, et al. Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-pick disease type B and B variant): literature review and report of new cases. Mol Genet Metab. 2016;118:206–213. doi: 10.1016/j.ymgme.2016.05.001. PubMed DOI

Thurberg BL, Wasserstein MP, Schiano T, O’Brien F. Liver and skin histopathology in adults with acid sphingomyelinase deficiency (Niemann-pick disease type B) Am J Surg Pathol. 2012;36:1234–1246. doi: 10.1097/PAS.0b013e31825793ff. PubMed DOI PMC

Sheth JJ, Sheth FJ, Oza NJ, Gambhir PS, Dave UP, Shah RC. Plasma chitotriosidase activity in children with lysosomal storage disorders. Indian J Pediatr. 2010;77:203–205. doi: 10.1007/s12098-009-0249-0. PubMed DOI

Kadali S, Kolusu A, Sunkara S, Gummadi MR, Undamatla J. Clinical evaluation of chitotriosidase enzyme activity in Gaucher and Niemann pick a/B diseases: a retrospective study from India. Clin Chim Acta. 2016;457:8–11. doi: 10.1016/j.cca.2016.03.004. PubMed DOI

Brinkman J, Wijburg FA, Hollak CE, et al. Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-pick disease. J Inherit Metab Dis. 2005;28:13–20. doi: 10.1007/s10545-005-4416-9. PubMed DOI

Cox GF, Clarke LA, Giugliani R, McGovern MM. Burden of illness in acid sphingomyelinase deficiency: a retrospective chart review of 100 patients. JIMD Rep. 2018. 10.1007/8904_2018_120. PubMed PMC

Labrune P, Bedossa P, Huguet P, Roset F, Vanier MT, Odievre M. Fatal liver failure in two children with Niemann-pick disease type B. J Pediatr Gastroenterol Nutr. 1991;13:104–109. doi: 10.1097/00005176-199107000-00020. PubMed DOI

Acuña M, Martínez P, Moraga C, He X, Moraga M, Hunter B, Nuernberg P, Gutiérrez RA, González M, Schuchman EH, Santos JL, Miquel JF, Mabe P, Zanlungo S. Epidemiological, clinical and biochemical characterization of the p.(Ala359Asp) SMPD1 variant causing Niemann-pick disease type B. Eur J Hum Genet. 2016;24:208–213. doi: 10.1038/ejhg.2015.89. PubMed DOI PMC

Tassoni JP, Jr, Fawaz KA, Johnston DE. Cirrhosis and portal hypertension in a patient with adult Niemann-pick disease. Gastroenterology. 1991;100:567–569. doi: 10.1016/0016-5085(91)90233-B. PubMed DOI

McGovern MM, Wasserstein MP, Aron A, Desnick RJ, Schuchman EH, Brodie SE. Ocular manifestations of Niemann-pick disease type B. Ophthalmology. 2004;111:1424–1427. doi: 10.1016/j.ophtha.2003.10.034. PubMed DOI

McGovern MM, Pohl-Worgall T, Deckelbaum RJ, et al. Lipid abnormalities in children with types a and B Niemann pick disease. J Pediatr. 2004;145:77–81. doi: 10.1016/j.jpeds.2004.02.048. PubMed DOI

Lee CY, Krimbou L, Vincent J. Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol. Hum Genet. 2003;12:552–562. PubMed

Mendelson DS, Wasserstein MP, Desnick RJ, et al. Type B Niemann-pick disease: findings at chest radiography, thin-section CT, and pulmonary function testing. Radiology. 2006;238:339–345. doi: 10.1148/radiol.2381041696. PubMed DOI

Nicholson AG, Florio R, Hansell DM, et al. Pulmonary involvement by Niemann-pick disease. A report of six cases. Histopathology. 2006;48:596–603. doi: 10.1111/j.1365-2559.2006.02355.x. PubMed DOI

Zampieri S, Filocamo M, Pianta A, et al. SMPD1 mutation update: database and comprehensive analysis of published and novel variants. Hum Mutat. 2016;37:139–147. doi: 10.1002/humu.22923. PubMed DOI

Simonaro CM, Desnick RJ, McGovern MM, Wasserstein MP, Schuchman EH. The demographics and distribution of type B Niemann-pick disease: novel mutations lead to new genotype/phenotype correlations. Am J Hum Genet. 2002;71:1413–1419. doi: 10.1086/345074. PubMed DOI PMC

Mihaylova V, Hantke J, Sinigerska I, et al. Highly variable neural involvement in sphingomyelinase-deficient Niemann-pick disease caused by an ancestral gypsy mutation. Brain. 2007;130(Pt 4):1050–1061. PubMed

Desnick JP, Kim J, He X, Wasserstein MP, Simonaro CM, Identification SEH. Characterization of eight novel SMPD1 mutations causing types a and B Niemann-pick disease. Mol Med. 2010;16:316–321. doi: 10.2119/molmed.2010.00017. PubMed DOI PMC

Zhang H, Wang Y, Gong Z, Li X, Qiu W, Han L, Ye J, Gu X. Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-deficient Niemann-pick disease. Orphanet J Rare Dis. 2013;8:15. doi: 10.1186/1750-1172-8-15. PubMed DOI PMC

Chuang WL, Pacheco J, Cooper S, et al. Lyso-sphingomyelin is elevated in dried blood spots of Niemann-pick B patients. Mol Genet Metab. 2014;111:209–211. doi: 10.1016/j.ymgme.2013.11.012. PubMed DOI

Voorink-Moret M, Goorden SMI, van Kuilenburg ABP, Wijburg FA, Ghauharali-van der Vlugt JMM, Beers-Stet FS, Zoetekouw A, Kulik W, Hollak CEM, Vaz FM. Rapid screening for lipid storage disorders using biochemical markers. Expert center data and review of the literature. Mol Genet Metab. 2018;123:76–84. doi: 10.1016/j.ymgme.2017.12.431. PubMed DOI

WelforRW GM, Lourenco CM, Mengel E, Marquardt T, Reunert J, Amraoui Y, Kolb SA, Morand O, Groenen P. Plasma lysosphingomyelin demonstrates great potential as a diagnostic biomarker for Niemann-pick disease type C in a retrospective study. PLoS One. 2014;9:e114669. doi: 10.1371/journal.pone.0114669. PubMed DOI PMC

Giese AK, Mascher H, Grittner U, Eichler S, Kramp G, Lukas J, Vruchte D, Al Eisa N, Cortina-Borja M, Porter FD, Platt FM, Rolfs A. A novel, highly sensitive and specific biomarker for Niemann-pick type C1 disease. Orphanet J Rare Dis. 2015;10:78. doi: 10.1186/s13023-015-0274-1. PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...