How Gaussian mixture modelling can help to verify reference intervals from laboratory data with a high proportion of pathological values
Author:
Hoffmann Georg1, Allmeier Nina1, Kuti Modupe23, Holdenrieder Stefan1, Trulson Inga1
Affiliation:
1. German Heart Center Munich , Institute of Laboratory Medicine , Munich , Germany 2. College of Medicine , University of Ibadan , Ibadan , Nigeria 3. Synlab Nigeria Laboratories , Lagos , Nigeria
Abstract
Abstract
Objectives
Although there are several indirect methods that can be used to verify reference limits, they have a common weakness in that they assume a low proportion of pathological values. This paper investigates whether a Gaussian decomposition algorithm can identify the non-pathological fraction even if it is not the main subset of mixed data.
Methods
All investigations are carried out in the R programming environment. The mclust package is used for Gaussian mixture modelling via the expectation maximization (EM) algorithm. For right-skewed distributions, logarithms of the original values are taken to approximate the Gaussian model. We use the Bayesian information criterion (BIC) for evaluation of the results. The reflimR and refineR packages serve as comparison procedures.
Results
We generate synthetic data mixtures with known normal distributions to demonstrate the feasibility and reliability of our approach. Application of the algorithm to real data from a Nigerian and a German population produces results, which help to interpret reference intervals of reflimR and refineR that are obviously too wide. In the first example, the mclust analysis of hemoglobin in Nigerian women supports the medical hypothesis that an anemia rate of more than 50 % leads to falsely low reference limits. Our algorithm proposes various scenarios based on the BIC values, one of which suggests reference limits that are close to published data for Nigeria but significantly lower than those established for the Caucasian population. In the second example, the standard statistical analysis of creatine kinase in German patients with predominantly cardiac diseases yields a reference interval that is clearly too wide. With mclust we identify overlapping fractions that explain this false result.
Conclusions
Gaussian mixture modelling does not replace standard methods for reference interval estimation but is a valuable adjunct when these methods produce discrepant or implausible results.
Publisher
Walter de Gruyter GmbH
Reference20 articles.
1. Horowitz, GL, Altaie, S, Boyd, JC, Ceriotti, F, Garg, G, Horn, P, et al.. EP28-A3C: Defining, establishing, and verifying reference intervals in the clinical laboratory; Approved Guideline - Third Edition. Vol. 28. No. 30. 3rd ed. Wayne: Clinical and Laboratory Standards Institute; 2010. 2. Ozarda, Y, Higgins, V, Adeli, K. Verification of reference intervals in routine clinical laboratories: practical challenges and recommendations. Clin Chem Lab Med 2018;57:30–7. https://doi.org/10.1515/cclm-2018-0059. 3. Jones, G, Haeckel, R, Loh, T, Sikaris, K, Streichert, T, Katayev, A, et al.. Indirect methods for reference interval determination: review and recommendations. Clin Chem Lab Med 2018;57:20–9. https://doi.org/10.1515/cclm-2018-0073. 4. Ozarda, Y, Ichihara, K, Jones, G, Streichert, T, Ahmadian, R. Comparison of reference intervals derived by direct and indirect methods based on compatible datasets obtained in Turkey. Clin Chim Acta 2021;520:95. https://doi.org/10.1016/j.cca.2021.05.030. 5. Haeckel, R, Wosniok, W, Streichert, T. Review of potentials and limitations of indirect approaches for estimating reference limits /intervals of quantitative procedures in laboratory medicine. J Lab Med 2021;45:35–53. https://doi.org/10.1515/labmed-2020-0131.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|