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Geographic Diversity in the Incidence of Human Prion Diseases - China, 2006-2019
Qi Shi1, Kang Xiao1, Liping Gao1
1National Key-Laboratory of Intelligent Tracking and Forecasting for Infectious Disease, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
Insights
Hospital referrals for human prion diseases (PrDs) to China's national surveillance increased significantly from 2006-2019. Surveillance data reveals geographical disparities in PrD case reporting across China.
Area of Science:
- Neurology
- Epidemiology
- Public Health
Background:
- Human prion diseases (PrDs) are rare, fatal neurodegenerative disorders.
- Comprehensive diagnostic analysis and surveillance are crucial for understanding PrD epidemiology.
- The Chinese National Surveillance for Creutzfeldt-Jakob Disease (CNS-CJD) monitors these rare conditions.
Purpose of the Study:
- To analyze hospital referral patterns for PrD cases to the CNS-CJD.
- To investigate geographical variations in PrD case reporting across China's provincial-level administrative divisions (PLADs).
- To assess the impact of surveillance on case detection.
Main Methods:
- Retrospective analysis of 1,970 PrD cases referred to CNS-CJD from 2006 to 2019.
- Evaluation of referral data from 344 hospitals across 29 PLADs.
- Statistical comparison of referral numbers and confirmed cases between monitored and non-monitored PLADs.
Main Results:
- A significant increase in referring hospitals was observed over the surveillance period.
- A small proportion of hospitals (12.2%) reported a majority (70.0%) of PrD cases.
- Referral numbers and case counts varied substantially across PLADs, with some regions showing higher reporting rates.
Conclusions:
- Geographical disparities in PrD recognition and reporting are evident across China.
- Major urban centers and monitored regions demonstrate higher referral rates.
- Enhanced surveillance strategies may be needed to address regional inequalities in PrD diagnosis.
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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