Pneumonia remains a major cause of child mortality in less developed countries. However, the accuracy of its prevalence and burden remains a challenge because disease data is often based on self-reports, resulting in measurement error in a form of under- and over-reporting. We propose hierarchical disease mapping approaches that permit measurement error, through different prior distributions of sensitivity and specificity. Proposed models were used to evaluate spatial variation of risk of pneumonia in children in Malawi. Results show that the true prevalence was 0.50 (95 CI: 0.4-0.66), however, estimates were dependent on sensitivity and specificity parameters. The estimated sensitivity was 0.76 (95% CI: 0.68-0.95), whereas specificity was 0.84 (95% CI: 0.72-0.93). A lower specificity underestimated the true prevalence, while sensitivity and specificity of greater or equal to 0.75 provided reliable and stable prevalence estimates. The spatial variation in disease risk changed little; however, misclassification of areas as high risk was visible.
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http://dx.doi.org/10.1016/j.sste.2015.11.002 | DOI Listing |
JMIR Public Health Surveill
January 2025
Center for Global Health, University of New Mexico Health Sciences Center, Albuquerque, NM, United States.
Background: Numerous studies have assessed the risk of SARS-CoV-2 exposure and infection among health care workers during the pandemic. However, far fewer studies have investigated the impact of SARS-CoV-2 on essential workers in other sectors. Moreover, guidance for maintaining a safely operating workplace in sectors outside of health care remains limited.
View Article and Find Full Text PDFBackground: The atherogenic index of plasma (AIP) is a newly identified metabolic marker for atherosclerosis. However, there are inconsistent conclusions regarding the relationship between AIP and hypertension.
Methods: The study subjects were sourced from the National Health and Nutrition Examination Survey (NHANES) database from 2017 to 2020.
PLoS One
January 2025
Manchester Cancer Research Centre, Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
Non-covalent protein-protein interactions are one of the most fundamental building blocks in cellular signalling pathways. Despite this, they have been historically hard to identify using conventional methods due to their often weak and transient nature. Using genetic code expansion and incorporation of commercially available unnatural amino acids, we have developed a highly accessible method whereby interactions between biotinylated ubiquitin-like protein (UBL) probes and their binding partners can be stabilised using ultraviolet (UV) light-induced crosslinks.
View Article and Find Full Text PDFPLoS One
January 2025
Department of Pathology, the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Background: Ras-GTPase-activating protein (GAP)-binding protein 1 (G3BP1) emerges as a pivotal oncogenic gene across various malignancies, notably including nasopharyngeal carcinoma (NPC). The use of automated image analysis tools for immunohistochemical (IHC) staining of particular proteins is highly beneficial, as it could reduce the burden on pathologists. Interestingly, there have been no prior studies that have examined G3BP1 IHC staining using digital pathology.
View Article and Find Full Text PDFIn 2019, the novel coronavirus swept the world, exposing the monitoring and early warning problems of the medical system. Computer-aided diagnosis models based on deep learning have good universality and can well alleviate these problems. However, traditional image processing methods may lead to high false positive rates, which is unacceptable in disease monitoring and early warning.
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