Literature DB >> 31332621

Obstructive sleep apnea and craniofacial appearance in MPS type I-Hurler children after hematopoietic stem cell transplantation.

Till Koehne1, Sarah Müller-Stöver2, Anja Köhn2, Katharina Stumpfe2, Susanne Lezius3, Carmen Schmid4, Zoltan Lukacs5, Bärbel Kahl-Nieke4, Nicole Muschol2.   

Abstract

OBJECTIVES: Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal storage disorder characterized by severe multi-systemic organ manifestations including obstructive sleep apnea syndrome (OSAS). Hematopoietic stem cell transplantation (HSCT) is the treatment of choice in severe MPS I (MPS IH, Hurler syndrome). However, the effect of HSCT on OSAS in MPS IH still remains unclear. The purpose of this study was to analyze respiratory patterns during sleep following HSCT in MPS IH children and to relate these findings to craniofacial abnormalities.
METHODS: Overnight polysomnographies of nine MPS IH children (mean age: 8.2 years) previously treated with HSCT were retrospectively analyzed. Magnetic resonance images of the head were assessed with regard to soft and hard tissue abnormalities of the upper respiratory tract.
RESULTS: The mean apnea hypopnea index (AHI) was 5.3 events/h (range, 0.3-12.2), and the majority of apnea/hypopneas were obstructive. Whereas two patients had severe OSAS (AHI > 10) and two moderate OSAS (5 > AHI < 10), five patients had no evidence of OSAS (AHI < 2.0). Donor cell chimerism was significantly lower in MPS IH patients with OSAS as compared to patients without OSAS (p < 0.001). The upper airway space and the maxilla were significantly smaller and the adenoids larger in MPS IH patients with OSAS as compared to those of non-OSAS patients.
CONCLUSION: OSAS was only observed in MPS IH patients with graft failure or low donor cell chimerism. Conversely, successful HSCT seems to ameliorate adenoid hyperplasia and maxillary constriction in MPS IH patients and thereby minimizes the risk of OSAS at least at younger ages.

Entities:  

Keywords:  Airway; Craniofacial; MRI; Mucopolysaccharidosis; Polysomnography

Mesh:

Year:  2019        PMID: 31332621     DOI: 10.1007/s11325-019-01900-9

Source DB:  PubMed          Journal:  Sleep Breath        ISSN: 1520-9512            Impact factor:   2.816


  25 in total

1.  Advances in the treatment of mucopolysaccharidosis type I.

Authors:  Joseph Muenzer; Amy Fisher
Journal:  N Engl J Med       Date:  2004-05-06       Impact factor: 91.245

2.  Patients with mucopolysaccharidosis have tendencies towards vertical facial growth.

Authors:  Fátima Roneiva Alves Fonseca; Dmitry José de Santana Sarmento; Paula Frassinetti Vasconcelos Medeiros; Denise Nóbrega Diniz; Maria Teresa Botti Rodrigues dos Santos
Journal:  J Oral Maxillofac Surg       Date:  2014-07-16       Impact factor: 1.895

3.  Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study.

Authors:  Mieke Aldenhoven; Robert F Wynn; Paul J Orchard; Anne O'Meara; Paul Veys; Alain Fischer; Vassili Valayannopoulos; Benedicte Neven; Attilio Rovelli; Vinod K Prasad; Jakub Tolar; Heather Allewelt; Simon A Jones; Rossella Parini; Marleen Renard; Victoria Bordon; Nico M Wulffraat; Tom J de Koning; Elsa G Shapiro; Joanne Kurtzberg; Jaap Jan Boelens
Journal:  Blood       Date:  2015-01-26       Impact factor: 22.113

4.  Orofacial features of Scheie (Hurler-Scheie) syndrome (alpha-L-iduronidase deficiency).

Authors:  O Keith; C Scully; G M Weidmann
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1990-07

5.  Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations.

Authors:  Piranit Nik Kantaputra; Hulya Kayserili; Yeliz Guven; Warissara Kantaputra; Mehmet C Balci; Pranoot Tanpaiboon; Napaporn Tananuvat; Anusha Uttarilli; Ashwin Dalal
Journal:  Am J Med Genet A       Date:  2014-03-27       Impact factor: 2.802

6.  Rapid maxillary expansion in children with obstructive sleep apnea syndrome: 12-month follow-up.

Authors:  Maria Pia Villa; Caterina Malagola; Jacopo Pagani; Marilisa Montesano; Alessandra Rizzoli; Christian Guilleminault; Roberto Ronchetti
Journal:  Sleep Med       Date:  2007-01-18       Impact factor: 3.492

7.  Polysomnographic characteristics in patients with mucopolysaccharidoses.

Authors:  Hsiang-Yu Lin; Ming-Ren Chen; Ching-Chi Lin; Chih-Ping Chen; Dar-Shong Lin; Chih-Kuang Chuang; Dau-Ming Niu; Jui-Hung Chang; Hung-Chang Lee; Shuan-Pei Lin
Journal:  Pediatr Pulmonol       Date:  2010-08-17

8.  Upper airway obstructive disease in mucopolysaccharidoses: polysomnography, computed tomography and nasal endoscopy findings.

Authors:  F Santamaria; M V Andreucci; G Parenti; M Polverino; D Viggiano; S Montella; A Cesaro; R Ciccarelli; B Capaldo; G Andria
Journal:  J Inherit Metab Dis       Date:  2007-06-14       Impact factor: 4.982

9.  Rules for scoring respiratory events in sleep: update of the 2007 AASM Manual for the Scoring of Sleep and Associated Events. Deliberations of the Sleep Apnea Definitions Task Force of the American Academy of Sleep Medicine.

Authors:  Richard B Berry; Rohit Budhiraja; Daniel J Gottlieb; David Gozal; Conrad Iber; Vishesh K Kapur; Carole L Marcus; Reena Mehra; Sairam Parthasarathy; Stuart F Quan; Susan Redline; Kingman P Strohl; Sally L Davidson Ward; Michelle M Tangredi
Journal:  J Clin Sleep Med       Date:  2012-10-15       Impact factor: 4.062

10.  The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK.

Authors:  David Moore; Martin J Connock; Ed Wraith; Christine Lavery
Journal:  Orphanet J Rare Dis       Date:  2008-09-16       Impact factor: 4.123

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  1 in total

Review 1.  Mucopolysaccharidosis Type I: Current Treatments, Limitations, and Prospects for Improvement.

Authors:  Christiane S Hampe; Jacob Wesley; Troy C Lund; Paul J Orchard; Lynda E Polgreen; Julie B Eisengart; Linda K McLoon; Sebahattin Cureoglu; Patricia Schachern; R Scott McIvor
Journal:  Biomolecules       Date:  2021-01-29
  1 in total

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