ArticleJournal of the American Statistical Association2024
Addressing Multiple Detection Limits with Semiparametric Cumulative Probability Models.
Article in Journal of the American Statistical Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- The Caribbean, Central and South America Network for HIV Epidemiology: 20 Years of HIV Research in the Region.Journal of the International AIDS Society · 2026Article
- Semiparametric outcome regression-based estimator of Mann-Whitney-type causal effect.BMC medical research methodology · 2026Article
- Article
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Authors and funding
6 authors.
Funding
Abstract
Detection limits (DLs), where a variable cannot be measured outside of a certain range, are common in research. DLs may vary across study sites or over time. Most approaches to handling DLs in response variables implicitly make strong parametric assumptions on the distribution of data outside DLs. We propose a new approach to deal with multiple DLs based on a widely used ordinal regression model, the cumulative probability model (CPM). The CPM is a rank-based, semiparametric linear transformation model that can handle mixed distributions of continuous and discrete outcome variables. These features are key for analyzing data with DLs because while observations inside DLs are continuous, those outside DLs are censored and generally put into discrete categories. With a single lower DL, CPMs assign values below the DL as having the lowest rank. With multiple DLs, the CPM likelihood can be modified to appropriately distribute probability mass. We demonstrate the use of CPMs with DLs via simulations and a data example. This work is motivated by a study investigating factors associated with HIV viral load 6 months after starting antiretroviral therapy in Latin America; 56% of observations are below lower DLs that vary across study sites and over time.
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