Segmentacion Basada en Colores vs. Estereologia: Una Comparacion Simple entre Dos Metodos Semiautomaticos de Analisis de Imagenes para la Cuantificacion del Colageno.
Currently, tissue processing and staining have been automated in the laboratory, and yet the subsequent analysis of histological images has not been done, with routine evaluations still performed by the trained eyes of a histologist. In addition, the evaluation or visual score not only implies a heavy workload, but also has inherent consequences on obtained data such as intra- and inter-observer variation, resulting in low efficiency in histological analysis (Riber-Hansen et al., 2012). In recent years, with the growing demands of quantitative analysis, digital image processing techniques attract more and more attention from morphologists. One of the most interesting situations in the field of histology and histopathology is the quantitative analysis of the collagen network in normal or pathological tissue, either in cases of hepatic or cardiac fibrosis or as a simple evaluation of the connective tissue of an organ. One of the most used methods to study the collagen network is Picrosirius Red Staining. Lattouf et al. (2014) affirmed that the picrosirius network associated with morphometric image analysis "remains the most powerful method to study and quantify collagen" phrase that was discussed by Marcos et al. (2015). Subsequently, the quantification of the types of collagens present in the tissue is possible through stereology. This conventional manual planimetry method has proven its value but it is laborious, and the result depends on the skill of the observer. However, semi-quantitative and semi-automated methods of collagen quantification have been introduced, one of these is the analysis of digital images (Daunoravicius et al., 2014).
Semi-automated analysis of images is being developed for helping specialists in analysis of histological images obtained from biopsies for diagnoses and prognoses determination. It provides users with functionalities and additional benefits to simple microscopic observation, replacing the subjective and qualitative visual evaluation--which could be affected by the quality of tissue staining--by more objectives, reproducible and quantifiable digital analyzes (Potts etal., 2010; Daunoravicius et al.), these advantages are similar to those presented by the stereological method. The semi-automated analysis of images is considered a more reliable method than the simple and traditional visual evaluation, which depends to a large extent on the experience of the researcher and, in general, can not be reproduced. Numerous recent studies show experimentally that automated evaluation can be used successfully in clinical practice and biomedical research (Kayser & Kayser, 2013; Ohlschlegel et al., 2013; Daunoravicius et al.; Webster & Dunstan, 2014). One of the useful semi-automated analyses to perform image analysis is the Color-Based Image Segmentation using a cluster of pixels. It consists of constructing a symbolic representation of the image: the image is described as homogeneous areas according to one or several attributes chosen a priori by the researcher (Belaid & Mourou, 2009). Color image segmentation is fundamental and critical for quantitative histological image analysis. The histological sections are segmented according to the color, shape or texture characteristics after being acquired with a high-resolution digital camera, and then classified using commonly supervised methods (Wu et al, 2015).
Several methods based on digital image processing and pattern recognition techniques have been proposed to address the problem of histological image segmentation. There are many existing approaches in literature that can be used to segment the histological image. These include methods based on clustering: A-Means and Mean Shift schemes based on mixed models (Chitade & Katiyar, 2010). To validate a new technique for quantifying collagen associated with a digital algorithm, the most frequent is to compare the results obtained from the subjective evaluation of the pathologist and validate it against the best clinically accepted method, however, Daunoravicius et al. affirm this is no longer valid. Another alternative is to compare the results with a more specific and precise method. In this sense, we propose the use of stereological methods, instead of the visual impression of the histologist. It was hypothesized that there is agreement between color segmentation and stereology to determine the amount of collagen. The objective of the study was to evaluate how well the methods--color-based image segmentation and stereology--agree on average, and how well they agree for the individuals.
MATERIAL AND METHOD
Preparation of the tissue and obtaining digital images.
Sections of mandibular tissue of Salmo salar were obtained and fixed in 10 % formaldehyde for 72 h at room temperature (22 [degrees]C). Then, they were dehydrated in a series of alcohols, clarified in xylol and embedded in Paraplast (Paraplast Plus embedding medium; melting point: 54 [degrees]C; Sigma-Aldrich Chemical Co., St Louis, MO, USA). Serial sections were made, 5 [micro]m thick, with a motorized rotary microtome Leica RM2255 (Leica Microsystems, Switzerland). Then, the sections were rehydrated, immersed in xylol (10 min), exposed to descending concentrations of ethanol (100 %, 96 %, 80 % and 70 %, all 15 s) and finally distilled water. Staining was performed using 0.1 % solution of Picrosirius red in a saturated aqueous solution of picric acid for one hour at room temperature (18 [degrees]C; Junqueira et al., 1979). Then, sections were rinsed in 0.01 NHCl for 2 min, dehydrated in ascending concentrations of ethanol (70 %, 80 %, 96 % and 100 %, each 10 s) and cleared in two stages in xylene, 10 min each one. Sections were covered with Entellan mounting medium (Merck, Darmstadt, Germany) and a glass cover slip. The mandibular tissue were observed by polarization microscopy using a Leica[R]DM5000B microscope (Leica Microsystems, Switzerland) equipped with a light circular polarized composed of a simple polarizer and a filter analyzer (Leica Microsystems, Switzerland). This filter was aligned so the background in the field of view would be as dark as possible. Collagen type III (fibrillarimmature) was identified by green birefringence, whereas collagen type I (dense-mature) was identified by yellowred birefringence (Junqueira et al. 1979). Digital images (40X) of mandibular tissue fields were obtained with a Leica[R]MC170HD digital camera using Leica Acquire v3.2 software for Mac OS X (Leica Microsystems, Switzerland) and with Digital Slide Scanner (Motic Easy Scan[R]).
Groups and Quantification of Collagen. For the study of quantification of collagen, the same 200 images (40X; 20 fields/per slide; 2048 x1536 pixels) were analyzed per group, which were evaluated by two different methods. i) Group 1: Color Based-Segmentation (Color Segmentation Plug In; EPFL, Lausanne, Switzerland; ImageJ32 v1.51p) (Schindelin et al., 2015). This ImageJ plugin allows a color image or a stack of color to be segmented by pixel clustering. The cluster of colors was defined manually by three users through the software interface. A-means clustering algorithm was used to identify collagen type I (red birefringence) and III (green birefringence) and both were considered the region of interest (ROI), separately. A-means is the clustering algorithm used to determine the natural spectral groupings present in a data set and it is one of the simplest unsupervised learning algorithms. It is a segregating technique. The role of K-means is divide data into k equally high-class clusters, and revenues the directory of the cluster to which it has allocated respectively remark (Fig. 1A) (Abdul Nazeer & Sebastian, 2009; Chitade & Katiyar). ii) Group 2: Stereology (Volume density: [V.sub.V]. System-Test [M.sub.36], STEPanizer Stereological Tools Cruz-Orive, 1993). The [V.sub.V] of collagen type I and III were estimated by point counting. The counting points-hits collagen were defined manually by the researcher according to the observation of collagen Type I or Type III through the software interface. The [M.sub.36] test system provided by the STEPanizer Stereological Tool software was used (Tschanz et al., 2011), which has 36 test points; the test line measures 18dand the test area measures 36.36[d.sup.2]. The overlapping program analyzed images from the Salmo salar jaw (Fig. 1B).
Statistic Analysis. The average concordance was evaluated by comparing the average of the differences of the measurements of the individuals by means t-Student (p<0.05), taking as hypothesis of nullity the no difference. To evaluate the concordance between individuals, or bias, the variability of the differences was evaluated with 95 % confidence intervals (CIs) calculated as the mean difference [+ or -] 1.96 x standard error of the differences (0 <CCI <1) (Altman & Bland, 1983; Bunce, 2009). The data analysis was performed using GraphPad Prism v. 7.0d for Mac OSX (GraphPad Software, San Diego CA).
The PicroSiurius stain confirmed the presence of collagen type I and III in the mandibular tissue of Salmo salar. The data analysis of average concordance showed that there is concordance of quantification of collagen type I (Fig. 2A) (p=0.0511) between the Color-Based Segmentation (15.85 [+ or -] 2.57; IC95%: 14 -17.69) and Stereology (17.97 [+ or -] 1.9; IC95%: 16.60 - 19.33) methods. In addition, there is concordance of quantification collagen type III (Fig. 2B) (p=0.9335) between the color segmentation (22.37 [+ or -] 2.51; IC95%: 20.56 - 24.17) and stereology (22.46 [+ or -] 2.28; IC95%: 20.82 - 24.09). Regarding the concordance between individuals during the determination of the amount of type I and III collagen, in both methods it was observed that 100 % of the data was included within the limits of agreement (LoA). Also, it is appreciated that the difference of the observations was around 0 for most of the assessments, starting from quantities of 12 to 20 % of type I collagen (Fig. 2C) and 19 to 25 % of type III collagen (Fig. 2D).
Currently, the Food and Drug Administration (FDA) of the United States has approved the use of several applications of image analysis of utility in biomedicine, pathology and histology, which indicates that the semi-automated or automated quantification of histological variables provides reliable and reproducible results with greater accuracy than visual evaluation (Rojo et al., 2009). The analysis of morphometric images is very influenced by the configuration of the thresholds, the increase and the resolution of the image (Huang et al., 2013), because it is essentially a two-dimensional procedure (Marcos et al.). In contrast, stereology uses test systems that are applied to two-dimensional images (as histological sections) in order to obtain the three-dimensional information that is inherent in all biological tissues (Marcos et al.). Due to the objective and independent nature of stereological methods, this method was used in this study as the gold standard or the reference method for comparative image analysis (Hadi et al., 2011; Daunoravicius et al.).
In our study we used one of the most used segmentation techniques for these images segmentation: the A-means clustering algorithm, and the objective was to evaluate the concordance in the determination of the amount of tissue collagen between two semi-automated methods frequently used in biomedical research (segmentation of image colors and stereology). Therefore, we evaluated the accuracy in obtaining data from the digital image analysis tools for the measurement of the fraction area corresponding to collagen type I and III in Salmo salar jaw biopsies stained with Picrosirius Red, considered by some researchers one of the most used methods to study and quantify the remodeling of the collagen network (Malkusch et al, 1995), and compared them with reference data obtained by stereology (point counting; [V.sub.V]) in the same images.
The results obtained in this study indicate the determination of the amount of collagen based on the segmentation of colors does not differ from the results obtained by stereology, either with respect to the group average or individual variation for collagen type I and III; this considering that the standard deviation is low and, therefore, the error of variability rate is really low and stable. In addition, good agreement was observed between methods in the assessment of collagen type I and much better in that of collagen type III. Also, shows that color-based segmentation and stereology represent an important tool in biomedical research, integrating the objectiveness of the measurements, high level of reproducibility, low cost, independence of human subjectivity and possibility of quantitative analysis of the different variables. These advantages were also affirmed by Wu et al.
The assessment of the amount of collagen through the application of point counting was defined manually by the researcher according to the presence of collagen type I or type III through the software interface (Fig. 1B). Therefore, a fundamental requirement is to improve the contrast of the structures that the researcher needs to evaluate. One of the objectives of the Picrosirius Stain was to improve the contrast of the human eye to determine the intersection points of collagen in the test system during stereological study, and to determine the natural spectral groupings shown in a data set in the K-means.
The Picrosirius Red stain has become a common way to study the collagen network. Most images that created by polarizer and filter analyzer were completely clear and some was contain signal noise ratio (SNR), which affected collagen detection, however, we believe this did not have an effect on our results, which was demonstrated and contrasted with the stereological data. The final result of tissue recognition matches the stereology data outcome comparing with others studies using different segmentation techniques comparing with other scientific results (Varshney et al., 2009).
The quantification method directly influences the estimation of the amount of collagen in a tissue, so it requires particular attention, especially when comparisons between control and experimental groups are required. The present study compared two methods for assessing collagen. According to the evidence there is concordance in the quantitative data obtained through the Semi-automated Method (Color-Based Segmentation) and Stereology (point counting), which proved to be accurate and sensitive for the quantification of collagen. The results--and possibly also the intergroup comparisons--of the collagen estimation depend directly on the quantification method used. The simple application of semi-automated tools in the analysis of images as it was done here can be recommended for the quantification of collagen, however it requires to have considerations mainly avoid including in the estimation to structures that are not of interest, which would over- or underestimate the amount of collagen--dependent on tissue integrity, staining protocol and adequate image acquisition --generating erroneous results. In conclusion, stereology and color-based image segmentation are powerful tools, which can be used (combined or complementary to each other) for quantify collagen in histological sections.
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Instituto de Biologia
Facultad de Ciencias
Pontificia Universidad Catolica de Valparaiso
Recibido : 29-04-2018
Paulo Salinas (1); Jorge Sanhueza (2) & Carlos Sandoval (3, 4)
(1) Institute of Biology, Faculty of Sciences, Pontificia Universidad Catolica de Valparaiso, Valparaiso, Chile.
(2) School of Medicine, Faculty of Sciences, Universidad Mayor, Temuco, Chile.
(3) Graduate School, Faculty of Veterinary Sciences, Universidad Austral de Chile, Valdivia, Chile.
(4) Veterinary Histopathology Center, Puerto Montt, Chile.
Caption: Fig. 1. A. User Interface of ImageJ. Evaluation of the amount of collagen through the application of Color- Based image analysis (Color Segmentation Plug-In; ImageJ v1.51u. National Institute of Health, USA). B. User Interface STEPanizer Stereological Tool. Evaluation of the amount of collagen through the application of Stereology through the point counting (Volume density; [V.sub.V]). The counting pointshits collagen were defined manually by the researcher according to the presence of Type I or Type III through the software interface.
Caption: Fig. 2. Superior row: demonstrate the average of the differences of the measurements of (A) collagen type I (p=0.0511) and (B) collagen type III (p=0.9335) of the individuals by means t-Student. Inferior row: Bland-Altman plot showing the difference against the average of Color Segmentation and Stereology measurements with limits of agreement (LoA; red lines) and Bias (blue line). In (C), this plot shows the agreement between methods to quantify collagen type I, demonstrate evidence of increasing variability of differences between methods, so the LoA is much wider as the amount of collagen type I in the tissue increases. In (D), this plot shows the agreement between methods to quantify collagen type III and demonstrate no relationship between discrepancy and the level of measurement of collagen type III, so that LoA are valid and there is concordance between both methods.
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|Author:||Salinas, Paulo; Sanhueza, Jorge; Sandoval, Carlos|
|Publication:||International Journal of Morphology|
|Date:||Sep 1, 2018|
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