Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa

Abstract Background Enzyme replacement therapy (ERT) with olipudase alfa, a recombinant human acid sphingomyelinase (rhASM), is being developed to treat patients with ASM deficiency (ASMD), commonly known as Niemann–Pick disease (NPD) types A or B. This study assessed the effect of ERT on lipid para...

Full description

Bibliographic Details
Main Authors: Bethanie Garside, Jan Hoong Ho, See Kwok, Yifen Liu, Shaishav Dhage, Rachelle Donn, Zohaib Iqbal, Simon A. Jones, Handrean Soran
Format: Article
Language:English
Published: BMC 2021-02-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:https://doi.org/10.1186/s13023-021-01739-y
id doaj-b7dc6ce787a046a7879d994e777be5c2
record_format Article
spelling doaj-b7dc6ce787a046a7879d994e777be5c22021-03-11T11:27:18ZengBMCOrphanet Journal of Rare Diseases1750-11722021-02-011611710.1186/s13023-021-01739-yChanges in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfaBethanie Garside0Jan Hoong Ho1See Kwok2Yifen Liu3Shaishav Dhage4Rachelle Donn5Zohaib Iqbal6Simon A. Jones7Handrean Soran8Lipid Research Group, Division of Cardiovascular Sciences, University of ManchesterLipid Research Group, Division of Cardiovascular Sciences, University of ManchesterLipid Research Group, Division of Cardiovascular Sciences, University of ManchesterLipid Research Group, Division of Cardiovascular Sciences, University of ManchesterCardiovascular Trials Unit, Manchester Royal Infirmary, Manchester University NHS Foundation TrustFaculty of Biology, Medicine and Health, University of ManchesterLipid Research Group, Division of Cardiovascular Sciences, University of ManchesterManchester Centre for Genomic Medicine, St Marys Hospital, Manchester University NHS Foundation TrustLipid Research Group, Division of Cardiovascular Sciences, University of ManchesterAbstract Background Enzyme replacement therapy (ERT) with olipudase alfa, a recombinant human acid sphingomyelinase (rhASM), is being developed to treat patients with ASM deficiency (ASMD), commonly known as Niemann–Pick disease (NPD) types A or B. This study assessed the effect of ERT on lipid parameters and inflammatory markers. Methods Serum and plasma samples from five adults with NPD type B (NPD-B) who received olipudase alfa ERT for 26 weeks were analysed. We also collected fasting blood samples from fifteen age- and sex-matched participants as reference and comparison group. We measured fasting lipid profile, apolipoproteins B48 and B100 (apoB48 and apoB100), apolipoprotein A1 (apoA1), proprotein convertase subtilisin/klexin type 9 (PCSK9) mass, oxidised low-density lipoprotein (oxLDL), small dense low-density lipoprotein cholesterol (sdLDL-C) and tumour necrosis factor α (TNF-α). Results Patients with NPD-B, compared with age and sex matched reference group, had higher triglycerides, PCSK9, apoB48, oxLDL and TNF-α and lower high density lipoprotein cholesterol (HDL-C) and apoA1. Treatment with ERT was associated with improved lipid parameters including total cholesterol, triglycerides, low density lipoprotein cholesterol (LDL-C), sdLDL-C, oxLDL and apoB100. Though there was an increase in apoA1, HDL-C was slightly reduced. TNF-α showed a reduction. ApoB100 decreased in parallel with a decrease in total serum PCSK9 mass after ERT. Conclusion This study demonstrated that patients with NPD-B had a proatherogenic lipid profile and higher circulating TNF-α compared to reference group. There was an improvement in dyslipidaemia after olipudase alfa. It was possible that reductions in LDL-C and apoB100 were driven by reductions in TNF-α and PCSK9 following ERT.https://doi.org/10.1186/s13023-021-01739-yAcid sphingomyelinase deficiencyApolipoprotein B100Proprotein convertase subtilisin/klexin type 9Tumour necrosis factor αLow density lipoprotein cholesterolEnzyme replacement therapy
collection DOAJ
language English
format Article
sources DOAJ
author Bethanie Garside
Jan Hoong Ho
See Kwok
Yifen Liu
Shaishav Dhage
Rachelle Donn
Zohaib Iqbal
Simon A. Jones
Handrean Soran
spellingShingle Bethanie Garside
Jan Hoong Ho
See Kwok
Yifen Liu
Shaishav Dhage
Rachelle Donn
Zohaib Iqbal
Simon A. Jones
Handrean Soran
Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
Orphanet Journal of Rare Diseases
Acid sphingomyelinase deficiency
Apolipoprotein B100
Proprotein convertase subtilisin/klexin type 9
Tumour necrosis factor α
Low density lipoprotein cholesterol
Enzyme replacement therapy
author_facet Bethanie Garside
Jan Hoong Ho
See Kwok
Yifen Liu
Shaishav Dhage
Rachelle Donn
Zohaib Iqbal
Simon A. Jones
Handrean Soran
author_sort Bethanie Garside
title Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
title_short Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
title_full Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
title_fullStr Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
title_full_unstemmed Changes in PCSK 9 and apolipoprotein B100 in Niemann–Pick disease after enzyme replacement therapy with olipudase alfa
title_sort changes in pcsk 9 and apolipoprotein b100 in niemann–pick disease after enzyme replacement therapy with olipudase alfa
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2021-02-01
description Abstract Background Enzyme replacement therapy (ERT) with olipudase alfa, a recombinant human acid sphingomyelinase (rhASM), is being developed to treat patients with ASM deficiency (ASMD), commonly known as Niemann–Pick disease (NPD) types A or B. This study assessed the effect of ERT on lipid parameters and inflammatory markers. Methods Serum and plasma samples from five adults with NPD type B (NPD-B) who received olipudase alfa ERT for 26 weeks were analysed. We also collected fasting blood samples from fifteen age- and sex-matched participants as reference and comparison group. We measured fasting lipid profile, apolipoproteins B48 and B100 (apoB48 and apoB100), apolipoprotein A1 (apoA1), proprotein convertase subtilisin/klexin type 9 (PCSK9) mass, oxidised low-density lipoprotein (oxLDL), small dense low-density lipoprotein cholesterol (sdLDL-C) and tumour necrosis factor α (TNF-α). Results Patients with NPD-B, compared with age and sex matched reference group, had higher triglycerides, PCSK9, apoB48, oxLDL and TNF-α and lower high density lipoprotein cholesterol (HDL-C) and apoA1. Treatment with ERT was associated with improved lipid parameters including total cholesterol, triglycerides, low density lipoprotein cholesterol (LDL-C), sdLDL-C, oxLDL and apoB100. Though there was an increase in apoA1, HDL-C was slightly reduced. TNF-α showed a reduction. ApoB100 decreased in parallel with a decrease in total serum PCSK9 mass after ERT. Conclusion This study demonstrated that patients with NPD-B had a proatherogenic lipid profile and higher circulating TNF-α compared to reference group. There was an improvement in dyslipidaemia after olipudase alfa. It was possible that reductions in LDL-C and apoB100 were driven by reductions in TNF-α and PCSK9 following ERT.
topic Acid sphingomyelinase deficiency
Apolipoprotein B100
Proprotein convertase subtilisin/klexin type 9
Tumour necrosis factor α
Low density lipoprotein cholesterol
Enzyme replacement therapy
url https://doi.org/10.1186/s13023-021-01739-y
work_keys_str_mv AT bethaniegarside changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT janhoongho changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT seekwok changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT yifenliu changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT shaishavdhage changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT rachelledonn changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT zohaibiqbal changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT simonajones changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
AT handreansoran changesinpcsk9andapolipoproteinb100inniemannpickdiseaseafterenzymereplacementtherapywitholipudasealfa
_version_ 1724225632124010496