Using virtual microscopy for the development of sampling strategies in quantitative histology and design-based stereology

. 2022 Jan ; 51 (1) : 3-22. [epub] 20211122

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid34806204

Grantová podpora
856620 Horizon 2020 Framework Programme
15-29241A Ministerstvo Zdravotnictví Ceské Republiky
AZV NU20J-08-00009 Ministerstvo Zdravotnictví Ceské Republiky
LO1503 Ministerstvo Školství, Mládeže a Tělovýchovy
GACR No. 1313420 Univerzita Karlova v Praze
Progres Q39 Univerzita Karlova v Praze
SVV 260 536 Univerzita Karlova v Praze
UNCE/MED/006 Univerzita Karlova v Praze
AMTMI CZ.02.1.01/0.0/0.0/17_048/0007280 European Regional Development Fund
FIND CZ.02.1.01/0.0/0.0/16_019/0000787 European Regional Development Fund

Only a fraction of specimens under study are usually selected for quantification in histology. Multilevel sampling or tissue probes, slides and fields of view (FOVs) in the regions of interest (ROIs) are required. In general, all parts of the organs under study should be given the same probability to be taken into account; that is, the sampling should be unbiased on all levels. The objective of our study was to provide an overview of the use of virtual microscopy in the context of developing sampling strategies of FOVs for stereological quantification. We elaborated this idea on 18 examples from multiple fields of histology, including quantification of extracellular matrix and muscle tissue, quantification of organ and tumour microvessels and tumour-infiltrating lymphocytes, assessing osseointegration of bone implants, healing of intestine anastomoses and osteochondral defects, counting brain neurons, counting nuclei in vitro cell cultures and others. We provided practical implications for the most common situations, such as exhaustive sampling of ROIs, sampling ROIs of different sizes, sampling the same ROIs for multiple histological methods, sampling more ROIs with variable intensities or using various objectives, multistage sampling and virtual sampling. Recommendations were provided for pilot studies on systematic uniform random sampling of FOVs as a part of optimizing the efficiency of histological quantification to prevent over- or undersampling. We critically discussed the pros and cons of using virtual sections for sampling FOVs from whole scanned sections. Our review demonstrated that whole slide scans of histological sections facilitate the design of sampling strategies for quantitative histology.

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