A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China

Abstract Background The study aim was to verify the feasibility of a diagnostic algorithm with the evaluation of beta glucocerebrosidase (GBA) activity on dried blood spots (DBS) in screening high-risk Gaucher disease (GD) children in China, and to investigate the GD prevalence in this selected popu...

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Main Authors: Ke Lei, Yanxia Zhao, Lirong Sun, Hui Liang, Ronghua Luo, Xiaojing Sun, Yanling Tao, Lijun Chen, Lingling Zhang, Aimin Li, Fu Li, Hongfang Ding
Format: Article
Language:English
Published: BMC 2018-04-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13023-018-0782-x
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spelling doaj-9e3c54d9db6a44fa89b016a18ca2ec8f2020-11-25T02:34:11ZengBMCOrphanet Journal of Rare Diseases1750-11722018-04-011311810.1186/s13023-018-0782-xA pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of ChinaKe Lei0Yanxia Zhao1Lirong Sun2Hui Liang3Ronghua Luo4Xiaojing Sun5Yanling Tao6Lijun Chen7Lingling Zhang8Aimin Li9Fu Li10Hongfang Ding11Pediatric Center, Affiliated Hospital of Qingdao UniversityPediatric Center, Affiliated Hospital of Qingdao UniversityPediatric Center, Affiliated Hospital of Qingdao UniversityDepartment of Pediatric Hematology, Qingdao Children’s HospitalDepartment of Pediatrics, Taian City Central HospitalDepartment of Pediatrics, Liaocheng People’s HospitalDepartment of Pediatrics, Affiliated Hospital of Jining Medical CollegeDepartment of Pediatric Endocrinology and Hematology, Shandong Provincial HospitalDepartment of Pediatrics, Linyi People’s HospitalDepartment of Pediatrics, Yantai Yuhuangding HospitalDepartment of Pediatric Hematology, Jinan Children’s HospitalDepartment of Pediatrics, Shengli Oilfield Central HospitalAbstract Background The study aim was to verify the feasibility of a diagnostic algorithm with the evaluation of beta glucocerebrosidase (GBA) activity on dried blood spots (DBS) in screening high-risk Gaucher disease (GD) children in China, and to investigate the GD prevalence in this selected population. Methods Children were recruited from 20 departments of pediatrics or children’s hospitals in Shandong Province, China, due to splenomegaly and/or thrombocytopenia associated with one or more of the following creteria: anemia, history of bone pain, monoclonal gammopathy of unknown significance (MGUS), polyclonal gammopathy and splenectomy. GBA activity on DBS was tested, and patients with DBS GBA activity under 30 nmol/h.ml were recalled to assess enzyme assay with gold standard and molecular GBA gene analysis on leukocytes. Results A total of 73 children (47 boys and 26 girls) were enrolled in this study. GBA activity DBS < 30 nmol/h.ml was found in 18 (23.7%) children among which four (three boys and one girl) were diagnosed as GD with a median age 1.5 years, and the prevalence in this pediatric population was 5.5% (1.5%~ 13.4%). Three new mutations of GBA found in the four GD patients, L264I, A100Cfs*7 and D399E, have not been reported before. Conclusions With evaluation of GBA activity on DBS as a preliminary screening method, the diagnostic algorithm used in this study is appropriate to make early diagnosis for GD patients with mild symptoms or atypical symptoms and avoid diagnosis delay. Trial registration Not applicable.http://link.springer.com/article/10.1186/s13023-018-0782-xGaucher DiseaseBeta glucocerebrosidaseDried blood spot
collection DOAJ
language English
format Article
sources DOAJ
author Ke Lei
Yanxia Zhao
Lirong Sun
Hui Liang
Ronghua Luo
Xiaojing Sun
Yanling Tao
Lijun Chen
Lingling Zhang
Aimin Li
Fu Li
Hongfang Ding
spellingShingle Ke Lei
Yanxia Zhao
Lirong Sun
Hui Liang
Ronghua Luo
Xiaojing Sun
Yanling Tao
Lijun Chen
Lingling Zhang
Aimin Li
Fu Li
Hongfang Ding
A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
Orphanet Journal of Rare Diseases
Gaucher Disease
Beta glucocerebrosidase
Dried blood spot
author_facet Ke Lei
Yanxia Zhao
Lirong Sun
Hui Liang
Ronghua Luo
Xiaojing Sun
Yanling Tao
Lijun Chen
Lingling Zhang
Aimin Li
Fu Li
Hongfang Ding
author_sort Ke Lei
title A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
title_short A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
title_full A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
title_fullStr A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
title_full_unstemmed A pilot screening of high-risk Gaucher disease children using dried blood spot methods in Shandong province of China
title_sort pilot screening of high-risk gaucher disease children using dried blood spot methods in shandong province of china
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2018-04-01
description Abstract Background The study aim was to verify the feasibility of a diagnostic algorithm with the evaluation of beta glucocerebrosidase (GBA) activity on dried blood spots (DBS) in screening high-risk Gaucher disease (GD) children in China, and to investigate the GD prevalence in this selected population. Methods Children were recruited from 20 departments of pediatrics or children’s hospitals in Shandong Province, China, due to splenomegaly and/or thrombocytopenia associated with one or more of the following creteria: anemia, history of bone pain, monoclonal gammopathy of unknown significance (MGUS), polyclonal gammopathy and splenectomy. GBA activity on DBS was tested, and patients with DBS GBA activity under 30 nmol/h.ml were recalled to assess enzyme assay with gold standard and molecular GBA gene analysis on leukocytes. Results A total of 73 children (47 boys and 26 girls) were enrolled in this study. GBA activity DBS < 30 nmol/h.ml was found in 18 (23.7%) children among which four (three boys and one girl) were diagnosed as GD with a median age 1.5 years, and the prevalence in this pediatric population was 5.5% (1.5%~ 13.4%). Three new mutations of GBA found in the four GD patients, L264I, A100Cfs*7 and D399E, have not been reported before. Conclusions With evaluation of GBA activity on DBS as a preliminary screening method, the diagnostic algorithm used in this study is appropriate to make early diagnosis for GD patients with mild symptoms or atypical symptoms and avoid diagnosis delay. Trial registration Not applicable.
topic Gaucher Disease
Beta glucocerebrosidase
Dried blood spot
url http://link.springer.com/article/10.1186/s13023-018-0782-x
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