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Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019

INTRODUCTION: Human prion diseases (PrDs) are rare, fatal encephalopathies requiring comprehensive diagnostic analysis. This study examines hospital referral patterns to the Chinese National Surveillance for Creutzfeldt-Jakob Disease (CNS-CJD) from 2006 to 2019. METHODS: We assessed 1,970 PrD cases...

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Autores principales: Shi, Qi, Xiao, Kang, Gao, Liping, Wu, Yuezhang, Zhou, Wei, Liang, Donglin, Chen, Cao, Dong, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Office of CCDCW, Chinese Center for Disease Control and Prevention 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652079/
https://www.ncbi.nlm.nih.gov/pubmed/38025513
http://dx.doi.org/10.46234/ccdcw2023.181
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author Shi, Qi
Xiao, Kang
Gao, Liping
Wu, Yuezhang
Zhou, Wei
Liang, Donglin
Chen, Cao
Dong, Xiaoping
author_facet Shi, Qi
Xiao, Kang
Gao, Liping
Wu, Yuezhang
Zhou, Wei
Liang, Donglin
Chen, Cao
Dong, Xiaoping
author_sort Shi, Qi
collection PubMed
description INTRODUCTION: Human prion diseases (PrDs) are rare, fatal encephalopathies requiring comprehensive diagnostic analysis. This study examines hospital referral patterns to the Chinese National Surveillance for Creutzfeldt-Jakob Disease (CNS-CJD) from 2006 to 2019. METHODS: We assessed 1,970 PrD cases referred by various hospitals to CNS-CJD. Referral distributions were analyzed based on provincial-level administrative divisions (PLADs). Differences in referral numbers and confirmed cases between monitored and non-monitored PLADs were statistically evaluated. RESULTS: The study included cases from 344 hospitals across 29 Chinese PLADs. Hospital referrals increased over the surveillance years: from 28.2 hospitals annually during 2006–2010, to 64 in 2011–2015, and 107 in 2016–2019. Of these, 12.2% (42/344) of hospitals reported ≥10 PrD cases, accounting for 70.0% (1,379/1,970) of total cases. Referral numbers varied across PLADs, with the top 5 of Beijing (41), Henan (26), Shanghai (21), Guangdong (21), and Jiangsu (21) leading. Additionally, 12 CJD-surveillance PLADs had more referring hospitals and PrD cases than the other 17 non-surveillance PLADs. CONCLUSIONS: Geographical variations in PrD recognition exist across Chinese PLADs, with certain regions and major cities reporting notably higher case numbers.
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spelling pubmed-106520792023-10-27 Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019 Shi, Qi Xiao, Kang Gao, Liping Wu, Yuezhang Zhou, Wei Liang, Donglin Chen, Cao Dong, Xiaoping China CDC Wkly Vital Surveillances INTRODUCTION: Human prion diseases (PrDs) are rare, fatal encephalopathies requiring comprehensive diagnostic analysis. This study examines hospital referral patterns to the Chinese National Surveillance for Creutzfeldt-Jakob Disease (CNS-CJD) from 2006 to 2019. METHODS: We assessed 1,970 PrD cases referred by various hospitals to CNS-CJD. Referral distributions were analyzed based on provincial-level administrative divisions (PLADs). Differences in referral numbers and confirmed cases between monitored and non-monitored PLADs were statistically evaluated. RESULTS: The study included cases from 344 hospitals across 29 Chinese PLADs. Hospital referrals increased over the surveillance years: from 28.2 hospitals annually during 2006–2010, to 64 in 2011–2015, and 107 in 2016–2019. Of these, 12.2% (42/344) of hospitals reported ≥10 PrD cases, accounting for 70.0% (1,379/1,970) of total cases. Referral numbers varied across PLADs, with the top 5 of Beijing (41), Henan (26), Shanghai (21), Guangdong (21), and Jiangsu (21) leading. Additionally, 12 CJD-surveillance PLADs had more referring hospitals and PrD cases than the other 17 non-surveillance PLADs. CONCLUSIONS: Geographical variations in PrD recognition exist across Chinese PLADs, with certain regions and major cities reporting notably higher case numbers. Editorial Office of CCDCW, Chinese Center for Disease Control and Prevention 2023-10-27 /pmc/articles/PMC10652079/ /pubmed/38025513 http://dx.doi.org/10.46234/ccdcw2023.181 Text en Copyright and License information: Editorial Office of CCDCW, Chinese Center for Disease Control and Prevention 2023 https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Vital Surveillances
Shi, Qi
Xiao, Kang
Gao, Liping
Wu, Yuezhang
Zhou, Wei
Liang, Donglin
Chen, Cao
Dong, Xiaoping
Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title_full Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title_fullStr Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title_full_unstemmed Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title_short Geographic Diversity in the Incidence of Human Prion Diseases — China, 2006–2019
title_sort geographic diversity in the incidence of human prion diseases — china, 2006–2019
topic Vital Surveillances
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652079/
https://www.ncbi.nlm.nih.gov/pubmed/38025513
http://dx.doi.org/10.46234/ccdcw2023.181
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