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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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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