Computer Image Analysis of Liver Biopsy Specimens in Patients with Heroin Abuse and Coinfection (Tuberculosis, HCV, HIV)

1. Introduction

The computer morphometry in histopathology is оnе of the most perspective directions in contemporary medicine including the hepatopathology. The potential advantages of measurement in histopathology have been recognized for many years [1]. The quantitative estimation has several advantages over conventional visual assessment such as objectivity and reproducibility [2]. The employment of modern optical equipment and special computer programs creates the possibilities for significant acceleration of quantitative analysis.

At present the computer morphometry has been rather intensively used to study liver changes of the patients with chronic viral hepatitis. The quantitative assessment of the fibrosis was performed mainly in chronic virus hepatitis C [3, 4, 5, 6, 7. 8, 9].

Many investigators considered that the quantitative evaluation of hepatic fibrosis was mostly useful for assessing the origin, location and the stage of fibrosis. Using the morphometric analysis is also very important for the correct evaluation of repeated biopsies [10]. Some investigators studied the changes in liver fibrosis after the interferon therapy [11, 12, 13]. This technique can be used in future for therapeutic trials by the estimation of the agents inhibiting the fibrosis progression [7].

Rates of fibrosis progression differ markedly in patients with HIV/HCV co-infection [14, 15, 16]. The natural history of hepatitis C virus infection in tuberculosis and in human immunodeficiency virus-infected patients has never been studied with the use of the computer morphometric analysis of liver fibrosis progression. In this chapter the changes of liver biopsies in patients with heroin abuse and infected by hepatitis C virus (HCV), human immunodeficiency virus (HIV), pulmonary tuberculosis (TB) were studied by the morphological and computer morphometric analysis.

2. Patients and methods

2.1. Patients

13 male patients with co-infection of pulmonary tuberculosis (TB), chronic viral hepatitis C (HCV) and human immunodeficiency virus (HIV) were investigated during the study. All the patients used also the injections of heroin (Table 1).

The patients started their history as a rule from heroin using (mean duration – 9.5 years) and later all of them acquired HCV (mean duration – 7.1 years), HIV (mean duration – 4.7 years) and TB at last (the duration of TB infection of the most part of patients was less than 1 year).

The diagnosis was established after careful examination of the patients: the anamneses of diseases and life, laboratory analyses, virological and morphological studies. Serum level of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) was expressed. The upper limit of normal (ULN) of ALT was 41 U/L, AST – 31 U/L.

2.2. Histological evaluation

To refine the diagnosis as well as for detection of the activity of pathological processes in the liver, aspiration biopsy was taken from all the patients. All liver biopsies were performed to the routine medical follow up program, using the standard Menghini procedure [17, 18]. Criteria for adequacy of the biopsy specimens included a core length of 10 mm and at least 5-6 portal tracts. So, only 9 biopsy specimens were used for further histological evaluation. Four biopsy specimens were fragmented and weren’t used (Table 1). Samples were formalin-fixed and paraffin-embedded. Serial paraffin sections were cut at 5 mcm. Hematoxylin-eosin and tolluidine blue stains were used.

Each biopsy for necro-inflammatory activity and fibrosis was assessed by two hepatologists. Knodell Histology Activity Index (HAI) was used to grade histopathological lesions [19]. HAI was graded as minimal (scores 1–3), mild (scores 4–8), moderate (scores 9–12), or severe hepatitis (scores 13–18). METAVIR group scoring system was used for detecting the stage of fibrosis [20]. Fibrosis was staged on the scale from F0 to F4, as follows: F0 = no fibrosis, F1 = portal fibrosis without septa, F2 = few septa, F3 = numerous septa without cirrhosis, F4 = cirrhosis. Only single patient showed any signs of cirrhosis. Fibrosis was also staged by Ishak scoring system[21]. In the Ishak scoring system interface hepatitis (piecemeal necrosis), focal necrosis in the lobule, portal inflammation were scored from 0 to 4, incomplete cirrhosis (bridging necrosis with occasional nodules) and cirrhosis were scored from 5 to 6.

Patient number	Sex	Age (years)	Biopsy number in next tables	Duration of infections (years)			Duration of heroin abuse (years)
TB	HCV	HIV
1	male	26	1	1	8	1	7
2	male	26	fragment	1	11	11	11
3	male	27	7	1	1	1	3
4	male	31	8	1	5	5	8
5	male	31	fragment	1	2	2	4
6	male	32	fragment	10	1	8	17
7	male	33	9	12	9	13	15
8	male	33	3	1	1	1	8
9	male	34	6	3	18	3	unknown
10	male	34	2	1	7	8	11
11	male	36	fragment	8	13	1	13
12	male	37	4	5	1	1	10
13	male	39	5	1	16	6	16

Table 1.

Characteristics of patients with heroin abuse and co-infection of TB, HCV, HIV. The patients are arranged according to their age.

2.3. Computer digital analysis

Quantitative morphometric analysis was performed using an image analysis system consisting of a microscope (Leica DM 2500) with attached digital camera (Leica DFC 320 R2) and a computer. Serial pictures of biopsy slices of patients with co-infection were photographed by light microscope and were saved electronically. Serial microphotographs of biopsies were made by an objective x20. The further process was performed with the computer program Adobe Photoshop CS 5.0. Serial microphotographs were mounted to receive the general picture of liver biopsy (Figure 1). The digital image was converted into a binary image. The two-dimensional patterns were measured by direct pixels counting on the binary images under simultaneous visual control of the light microscopy.

Figure 1.

General picture of the liver biopsy composed by computer microscopy (Obj. x20) using Adobe Photoshop CS 5.0. Total area of the biopsy is 11449177 pixels

Three main parameters were used for quantitative evaluation: the total area of portal zones, the total area of intralobular infiltrates and necroses, as well as the total area of hepatic vessels (central and sublobular veins). We considered the total amount of these main parameters as non-parenchymal elements. Liver plates and sinusoids were attributed to the hepatic parenchyma.

The measurement of portions (in percentages) of portal area, foci of intralobular necroses, and vessels was estimated.

2.4. Statistical analysis

Statistical analysis was performed by tabulated processor Microsoft Excel 2003 and STATISTIKA 9.0.

3. Results

3.1. Features of histopathological structure of biopsies

Morphological analysis of liver biopsies of the patients – heroin addicts with tuberculosis (TB) and virus (HCV, HIV) co-infection showed that the extension of portal zones, the damage of limiting plates of liver cells and the formation of piecemeal and bridging necroses took place practically in all biopsies (Figure 2).

Figure 2.

Subfigure with two images. Section of the liver biopsy specimen of a patient with co-infection (TB, HCV, HIV) and heroin abuse. Variants (a, b) of the development of interface hepatitis with piecemeal necrosis at the peripheral zone of portal tract. Hematoxylin-eosin. Obj. x40

The peripheral regions of the portal zones were usually densely infiltrated by lymphocytes and mononuclear histiocytes (Figure 2). Sometimes the lymphoid aggregates adjacent to the damaged bile ducts were formed. Dense connective tissue elements developed more often around the portal vessels (portal veins and hepatic arteries).

The appearance of focal lymphohistiocyte infiltrates and the formation of numerous intralobular necroses, containing hepatocytes, surrounded by lymphocytes (encircled hepatocytes) were typical to peripheral and middle zones of liver lobules (Figure 3).

Figure 3.

Subfigure with two images. Section of the liver biopsy specimen of a patient with co-infection (TB, HCV, HIV) and heroin abuse. Variants (a, b) of the development of intralobular necroses containing encircled hepatocytes at the middle part of liver lobule. Hematoxylin-eosin. Obj. x40

In the liver parenchyma the narrowing of sinusoids, as without of inflammatory infiltration signs and with the elements of lymphohistiocyte infiltration and chains of lymphocytes inside of them, was predominated (Figure 4).

There were features of moderate protein and vacuole dystrophia in all biopsies. In two cases some hepatocytes contained large lipid inclusions (Figure 5). Disturbance of the lobular architecture was observed only in one biopsy (Figure 6).

Figure 4.

Section of the liver biopsy specimen of a patient with co-infection (TB, HCV, HIV) and heroin abuse. Severe infiltration of intralobular sinusoids by lymphocytes and histiocytes at the peripheral zone of liver lobule. Hematoxylin-eosin. Obj. x20

Figure 5.

Section of the liver biopsy specimen of a patient with co-infection (TB, HCV, HIV) and heroin abuse. Expansion and infiltration of portal areas, presence of intralobular necroses at the middle zone of liver lobules, deposition of lipid droplets were in some hepatocytes. Hematoxylin-eosin. Obj. x10

Figure 6.

Section of the liver biopsy specimen of a patient with co-infection (TB, HCV, HIV) and heroin abuse. Strong development of bridging fibroses and disturbance of the lobular architecture. Hematoxylin-eosin. Obj. x10

3.2. Quantitative image analysis for evaluation of pathological changes in liver biopsy structure

Quantitative computer image morphometric analysis included three indexes. We calculated separately the square (in pixels) occupied by portal zones, the square of intralobular focal infiltrates and necroses and the square of hepatic vessels (central and sublobular veins).

The portal areas were divided into two groups: the portal zones with primary formation of piece-meal necroses and the portal zones with primary formation of bridging necroses. We took into account the calculation of portal zones fragments and septa. We also subdivided the intralobular damages in liver in two groups: the focal lymphohistiocyte infiltrates without hepatocytes and the intralobular piecemeal necroses with encircled hepatocytes.

As for hepatic vein, we separately considered terminal hepatic veins (central veins) and sublobular veins. In each case we estimated the relative square of the above-mentioned indexes in pixels and then calculated the specific parts in percents to the total square of biopsy.

We assigned the total sum of a specific part of portal zones, the specific part of intralobular focal infiltrates and necroses and the specific part of the hepatic veins as non-parenchymal elements. Respectively, the hepatic plates and sinusoids were remained in the composition of the parenchyma.

Then we calculated the parenchyma indexes as the relation of non-parenchymal elements to the parenchyma; these indexes characterized a certain degree of the replacement of the functioning hepatic tissue.

The data obtained were summarized in the Tables 2, 4, 5, 6 and 7. The samples of biopsies were arranged in sequence of increasing of non-parenchymal elements in bioptats.

The control group included the analysis of cohort of the patients with the monoinfection of chronic virus hepatitis C (Table 3). The morphometric analysis of liver structure of the patients belonging to given group was made earlier with the use of the method of the stereometric point morphometry [8].

3.2.1. The general characterization of morphometric data

The analysis showed that the specific part of non-parenchymal elements strongly varied in the group of the patients with co-infection and heroin abuse: from 2.65% to 27.43% (Table 2). Mean value of non-parenchymal elements was 12.08±2.38. The specific part of non-parenchymal elements varied in cases of monoinfection of hepatitis C with the different degree of activity from 2.16% до 11.93%, the mean value was 6.94±0.77. Thus, the mean value of non-parenchymal elements of liver biopsy of the patients – heroin addicts with co-infection exceeded the mean value of non-parenchymal elements in liver biopsy of the patients with monoinfection of hepatitis C (HСV) in 1.74 times. The maximal value of the specific part of non-parenchymal elements in case of co-infection was in 2.29 times higher than in cases of monoinfection HCV (Tables 2 and 3).

Biopsynumber	Parenchymal elements, %	Non-parenchymal elements, %	Ratio of non-parenchymal elements	Total area of portal zones, %	Total area of spotty infiltrates ,%	Total area of hepatic veins, %	Chains of lymphocytes (absent or present)
1	97,35	2,65	0,03	1,86	0,52	0,27	-
2	93,39	6,71	0,07	5,80	0,74	0,17	+
3	93,07	6,93	0,07	6,43	0,21	0,27	-
4	90,73	9,27	0,10	7,59	1,33	0,35	+
5	90,52	9,48	0,10	7,93	0,46	1,08	-
6	88,87	11,13	0,13	10,41	0,37	0,35	+
7	83,72	16,28	0,19	14,52	1,53	0,53	+
8	81,19	18,81	0,23	17,99	0,75	0,07	+
9	72,57	27,43	0,38	27,16	0,31	0	+

Table 2.

Quantitative characteristics of liver biopsy specimens of patients with heroin abuse and co-infection of TB, HCV and HIV by computer morphometric analysis

Biopsynumber	ALT activity (U/L)	Total area of morphometry (points of intersections)	Total number of microscopic fields(SU)(x400)	Parenchymal elements, %	Non-parenchymal elements, %	Ratio of non-parenchymal elements	Total area of portal area, %	Total area of spotty infiltrates ,%	Total area of hepatic veins, %	Chains of lymphocytes (absent or present)
1	15,	29450	95	97,84	2,16	0,02	1,79	0,05	0,32	-
2	20	18910	61	97,54	2,46	0,03	2,00	0,25	0,21	-
3	57	37690	126	96,49	3,51	0,04	2,30	0,46	0,75	-
4	14	17980	58	96,40	3,60	0,04	3,18	0,01	0,42	-
5	26	46190	149	95,70	4,30	0,04	3,15	0,12	1,02	-
6	104	70060	226	95,37	4,63	0,05	3,25	0,30	1,09	-
7	15	86800	280	95,30	4,70	0,05	2,91	0,02	1,77	-
8	42	37820	122	94,94	5,06	0,05	3,81	0,26	1,00	-
9	35	80290	259	94,82	5,18	0,05	3,93	0,84	0,41	+
10	441	89900	290	93,36	6,64	0,07	3,29	2,02	1,32	+
11	214	54560	176	91,33	8,67	0,09	7,24	0,89	0,55	-
12	187	70680	228	90,54	9,46	0,10	7,57	1,76	0,13	+
13	333	47720	152	90,32	9,68	0,11	7,51	1,17	1,00	-
14	107	32860	106	90,29	9,71	0,11	8,32	1,02	0,37	-
15	38	53514	193	89,44	10,56	0,12	6,23	2,61	1,71	+
16	122	49600	160	89,11	10,89	0,12	9,07	1,27	0,54	+
17	596	75330	243	88,24	11,76	0,13	9,26	1,56	0,94	+
18	162	60760	196	88,07	11,93	0,14	11,49	0,44	0,00	+

Table 3.

Quantitative characteristics of liver biopsy specimens of the patients with monoinfection of chronic hepatitis C by stereometric point morphometry

We made the comparative analysis of histopathological changes in liver biopsy structure in the group of the patients – heroin addicts and co-infected using the standard semi quantitative methods of the Ishak score evaluation (Table 4).

We determined the histological activity index HAI according to Knodell [19]. The stages of the fibrosis development were defined by two ways: with the use of the research group French METAVIR [20] recommendations and with Ishak method [21]. Under the METAVIR system we evaluated the fibroses using five indexes where the maximal evaluation was 4 scores (F4 – cirrhosis). It consisted 6 scores (F6 – cirrhosis) according the Ishak system.

Standard semi quantitative analysis methods for the most part of biopsies (6 patients from 9) made possible to determine the same fibrosis stage: F3 according to the Ishak system and F2 according to the METAVIR system (Table 4).

Biopsynumber	Non-parenchymal elements, %	HAI by score Knodell	Stage of fibrosis by score Ishak	Stage of fibrosis by score METAVIR
1	2,65	8	F3	F2
2	6,71	8	F3	F2
3	6,93	8	F3	F2
4	9,27	9	F3	F2
5	9,48	10	F3	F2
6	11,13	12	F3	F2
7	16,28	15	F4	F3
8	18,81	11	F3	F2
9	27,43	16	F5	F4

Table 4.

Comparative characteristics of non-parenchymal elements specific parts, grading of histopathological lesions (HAI) and the stages of fibrosis in liver biopsy specimens of the patients with heroin abuse and co-infection of TB, HCV and HIV by computer morphometry and semi quantitative evaluation

At that time the quantitative computer image morphometric analysis showed (Table 2) that among studied biopsies the specific parts of non-parenchymal elements differed significantly in various biopsies at the same fibrosis stages.

The minimal value of the specific part of non-parenchymal elements was 2.65%. These values were 6.71% и 6.93% (two biopsy specimens), 9.27% and 9.48% (two other specimens of biopsy) and 11.13% (one biopsy specimen). Thus, in this case the methods of the semi quantitative score evaluation reflected only common regularities of the process of the fibrosis development. Meanwhile, the quantitative value of fibrosis was very essential for decision making of the medical treatment tactic and the estimation of the medical treatment effectiveness.

The quantitative value of fibrosis is especially important in the process of repeated studies for the determination of positive or negative dynamics of the fibrosis development. The histological activity index HAI according to Knodell proved to be more informative. HAI increased gradually from 8 to 16 points in accordance with the increasing of specific parts of non-parenchymal elements in biopsies.

                               

3.2.2. Computer image analysis of portal zones

The majority of non-parenchymal elements were situated in portal zones. Therefore these indexes were analyzed in details (Table 5).

Biopsy number	Total area of non-parenchymal elements, %	Total area of portal zones		Portal area with piecemeal necroses				Portal area with bridging necroses
%	Number per biopsy	Total area, %	Number per biopsy	Minimal size, %	Maximal size, %	Total area, %	Number per biopsy	Minimal size, %	Maximal size, %
1	2,65	1,86	5	0,00	0	0	0	1,86	5	0,14	0,99
2	6,71	5,80	13	2,98	5	0,10	0,86	2,82	8	0,10	1,23
3	6,93	6,43	7	0,18	2	0,06	0,12	6,25	5	0,01	3,93
4	9,27	7,59	9	4,94	4	0,16	2,38	2,65	5	0,14	0,97
5	9,48	7,93	8	4,89	4	0,90	1,45	3,04	4	0,37	1,35
6	11,13	10,41	12	0,62	2	0,19	0,42	9,79	10	0,16	2,92
7	16,28	14,52	12	1,13	2	0,47	0,66	13,39	10	0,12	4,51
8	18,81	17,99	5	7,92	4	1,17	3,37	10,07	1	0,01	10,07
9	27,43	27,16	18	11,17	8	0,25	2,39	15,96	10	0,17	4,34

Table 5.

Quantitative characteristics of portal zones in liver biopsy specimens of the patients with heroin abuse and co-infection of TB, HCV and HIV by computer morphometric analysis

The amount of portal zones studied in each biopsy varied from 5 to 18. It depended on the total biopsy volume. The mean value of the portal zones number was 9.8 9±1.34. The amount of portal zones with piecemeal necroses varied from 2 to 8 (mean value was 3.44±0.72). The amount of portal zones with the septa and bridging necroses was more significant, it changed from 1 to 10 (mean value was 6.44±1.01).

In one case (biopsy specimen № 8) the portal zone included several portal tracts forming the extensive confluent bridging necrosis.Thus, the amount of portal zones with bridging necroses (6.44) exceeded in 1.87 times the amount of portal zones with piecemeal necroses (3.44).

The total specific part of portal zones varied from 1.86% to 27.16% (mean value was 11.08±2.42) (Table 5).

The specific part of portal zones with piecemeal necroses varied from 0.18% to 11.17% (mean value was 3.76±1.21). The minimal size of such portal zones characterized mainly its fragment, it changed from 0.06% to 0.9% (mean value is 0.37±0.13). The maximal sizes of such portal zones characterized in general the degree of the portal zone extension, they changed from 0.12% to 3.37% (mean value was 1.29±0.37).

The specific part of the portal zones with bridging necroses (Table 5) changed from1.86% to 15.96% (mean value was 7.31±1.63). Thus, the specific part of portal zones with bridging necroses was practically in 2 times (1.94) more than the specific part of portal zones with piecemeal necroses.

The minimal size of portal zones with bridging necroses characterized in general the septa fragments, it changed from 0.01% to 0.37% (mean value was 0.13±0.03). The maximal size reflected more correctly the specific part of the portal zones with bridging necroses, it changed from 0.97% to 10.07% (mean value was 3.37±0.91).

The quantitative computer image morphometric analysis showed that the significant extension of portal zones with the destruction of the limiting plate and the development of piecemeal or bridging necroses took place in all bioptats of this patients group. In addition the specific part of portal zones with bridging necroses exceeded considerably (in 1.9 times) the specific part of portal zones with piecemeal necroses.

For comparison: the total specific part of portal zones changed from 1.79% tо 11.49% (mеan value was 5.35±0.68) at chronic hepatitis C monoinfection (Table 3).

Thus, the specific part of portal zones of liver biopsies of the patients – heroine addicts with tuberculosis and virus (HCV, HIV) co-infection was 2.07 times higher than the specific part of portal zones of liver biopsies of the patients with the monoinfection HCV.

Moreover the bridging and piecemeal necroses were absent in the liver of the patients with monoinfection HCV under minimal and low activity. Their appearance was noticed only if

the value of specific parts of non-parenchymal elements exceeded 4.7%.

We have not observed any difference between the amounts of piecemeal and bridging necroses in biopsy specimens with monoinfection HCV.

3.2.3. Сomputer image analysis of intralobular infiltrates and necroses

We analyzed the morphometric indexes of intralobular infiltrates and necroses (Table 6).

Intralobular necroses presented in all biopsies, their number varied from 6 to 38 (mean value was 16.33±3.42). The amount of focal intralobular lymphohistiocyte infiltrates was significantly less in comparison with the intralobular necroses containing encircled hepatocytes.

The total number of focal intralobular infiltrates varied in different biopsies from 1 to 11 (mеan value was 3.67±1.09), whereas the total number of intralobular piecemeal necroses varied from 4 to 28 (mеan value was 12.78±2.5).

The relation between piecemeal necroses and focal intralobular infiltrates was especially demonstrative (Table 6). The number of piecemeal necroses in each biopsy was in several times more (up to 10 times) than the number of focal necroses. The total number of intralobular piecemeal necroses was 115, whereas the number of focal intralobular infiltrates was only 33, i.e. in 3.48 times less.

Biopsynumber	Total area of non-parenchymal elements, %	Total area of intralobular necroses, %	Total number of intralobular necroses perbiopsy	Focal lymphohistiocyte infiltrates				Intralobular necroses with encircled hepatocytes (piecemeal necroses)
Total area ,%	Total number per biopsy	Minimal size, %	Maximal size, %	Total area, %	Total number per biopsy	Minimal size, %	Maximal size, %
1	2,65	0,52	8	0,01	1	0,01	0,01	0,51	7	0,04	0,18
2	6,71	0,74	22	0,03	6	0	0,01	0,71	16	0,02	0,11
3	6,93	0,21	6	0,05	2	0,02	0,04	0,16	4	0,02	0,08
4	9,27	1,33	28	0,09	6	0,01	0,02	1,24	22	0,02	0,25
5	9,48	0,46	10	0,01	1	0,01	0,01	0,45	9	0,02	0,12
6	11,13	0,37	16	0,03	3	0,01	0,01	0,34	13	0,01	0,06
7	16,28	1,53	38	0,10	11	0,01	0,08	1,52	28	0,01	0,36
8	18,81	0,75	10	0	0	0	0	0,75	10	0,06	0,11
9	27,43	0,31	9	0,04	3	0,01	0,02	0,28	6	0,03	0,06

Table 6.

Quantitative characteristics of intralobular necroses in the liver biopsy specimens of the patients with heroin abuse and co-infection of TB, HCV and HIV by computer morphometric analysis

The total specific part of intralobular necroses varied from 0.21% to 1.53% (mеan value was 0.69±0.14). The specific part of the focal intralobular infiltrates varied from 0.01% to 0.1% (mеan value was 0.04±0.01). The size of the minimal infiltrate was only 0.01%, the size of the maximal infiltrate was 0.08% (mеan value was 0.02±0.01).

The total specific part of intralobular piecemeal necroses varied from 0.16% to 1.52% (mеan value was 0.66±0.14). The minimal size of the specific part of intralobular piecemeal necroses was 0.01% (mеan value was 0.03±0.01), whereas their maximal size was 0.36 % (mеan value was 0.15±0.02).

The analysis of the total biopsy specimen (Figure 1) allowed attributing the topography of the intralobular necroses distribution. Thus, under the middle degree of the parenchyma injury (HAI according to Knodell system up to 10 points) the small lymphohistiocyte infiltrates dominated in periportal zones of lobules. Under the high activity of the process (HAI according to Knodell scoring system exceeded 10 points) the large piecemeal necroses dominated, they arranged mainly in the middle zones of lobules.

Hepatocytes surrounded by lymphocytes were well noticeable in large piecemeal necroses (Figure 3b); it is perhaps connected with hepatocytes death, mediated by lymphocytes.

It is typically that the inflammatory infiltration of sinusoids and the formation “chains” of lymphocytes in them are mostly expressed in large piecemeal necroses (Figure 4).

So, the histological activity index HAI according to Knodell reached 15 points, the total number of intralobular necroses reached 38 (28 from them were referred to piecemeal necroses) in the biopsy № 7 (Tables 4 and 6). Remarkably that during the cirrhosis development (biopsy № 9, fibrosis stage according to the METAVIR system scale was F4 – cirrhosis) the total number of intralobular necroses considerably reduced (6 piecemeal necroses and 3 focal infiltrates in one large biopsy; see Figure 6).

3.2.4. Computer image analysis of hepatic vessels

The amount of venous vessels in biopsy samples varied from 2 to 7 (mean value was 3.33±0.63). The central veins with endothelium which are often damaged predominated in all biopsies (Table 7).

Biopsynumber	Total area of non-parenchymal elements, %	Total area of hepatic vessels ,%	Total number of hepatic vessels per biopsy	Terminal hepatic veins (central veins)				Sublobular veins
Total area ,%	Number per biopsy	Minimal size , %	Maximal size, %	Total area, %	Number per biopsy	Minimal size, %	Maximal size, %
1	2,65	0,27	4	0,27	4	0,09	0,11	0	0	0	0
2	6,71	0,17	2	0,17	2	0,03	0,14	0	0	0	0
3	6,93	0,27	3	0,27	3	0,03	0,18	0	0	0	0
4	9,27	0,35	4	0,35	4	0,07	0,11	0	0	0	0
5	9,48	1,08	5	0,13	4	0,02	0,05	0,95	1	0,95	0,95
6	11,13	0,35	7	0,35	7	0,01	0,11	0	0	0	0
7	16,28	0,53	3	0	0	0	0	0,53	3	0,04	0,31
8	18,81	0,07	2	0,07	2	0,03	0,04	0	0	0	0
9	27,43	0	0	0	0	0	0	0	0	0	0

Table 7.

Quantitative characteristics of hepatic vessels in liver biopsy specimens of the patients with heroin abuse and co-infection of TB, HCV and HIV by computer morphometric analysis

Sublobular veins were observed only in two biopsies, perhaps they did not get into biopsies because of large sizes in comparison with central veins.

The total specific part of the hepatic vessels varied from 0.07% to 1.08% (mean value was 0.34±0.1). The specific part of the central veins varied from 0.17% tо 0.35% (mean value was 0.18±0.04). The minimal size of the central vein was 0.01% (mean value was 0.03±0.01), the maximal size was 0.18% (mean value was 0.08±0.02). The specific part of sublobular veins reached 1.48%, maximal size – 0.95%.

On the whole it is possible to note the tendencies to the stable extension of vessels and the

damage of its internal walls. In addition, the sharp narrowing of intralobular sinusoids adjacent to above mentioned vessels, took part in the contribution of the impairment of the processes of the microcirculation inside of liver lobules. Perhaps the worsening of microcirculation lead to the bypass ways of the circulation, this may be one of the reasons of bridging necroses development.

3.3. Investigation of activity of alanin aminotransferase (ALT) and aspartate aminotransferase (AST)

The measurement of liver enzyme activities (serum ALT and AST) are important for diagnosis and assessment of liver diseases in clinical practice. However, ALT levels fluctuate in chronic HCV infection and may fall into the normal range [22].The use of many medications have been associated with elevated ALT levels [23]. In chronic hepatocellular injury, ALT increasing is more typical than AST. However, when the fibrosis progresses, ALT activity typically declines, and the ratio of AST to ALT gradually increases [24], especially during the development of cirrhosis [25,26].

We observed the increasing of the ALT and AST levels practically among all the patients (Table 8).

Biopsy number	Activity of ALT (U/L)	Activity of AST (U/L)	Ratio of AST/ALT
1	90	48	0,53
2	36	32	0,88
3	45	42	0,93
4	140	90	0,64
5	162	179	1,10
6	48	39	0,81
7	90	68	0,75
8	88	93	1,05
9	106	84	0,79

Table 8.

Activity of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in liver biopsy specimens of the patients with heroin abuse and co-infection of TB, HCV and HIV

So, the ALT level changed from 36 to 162 points (mean value was 89.4±13.45). The AST level varied from 32 to179 points (mean value was 75±14.25). The AST/ALT ratio varied from 0.53 to 1.10 points (mean value was 0.83±0.06).

The mostly expressed increase of ALT and AST levels was discovered in the patients with the samples of biopsy having the specific part of non-parenchymal elements up to 10% (Table 8, samples of biopsies № 4 and № 5). As a rule the ferment activity rather reduced under the fibrosis intensification. The AST/ALT ratio was increased in 3 patients. In other cases it was closer to the upper border of the normal level.

We have not discovered any direct interconnections between the ferment activity levels and the sizes of the specific parts of intralobular necroses. The intralobular piecemeal necroses were dominant in this group of the patients; perhaps, the hepatocytes destruction was caused by the special mechanism of the cell death (apoptosis).

4. Discussion

Detailed information about natural history of HIV/HCV co-infection is discussed in special review article [27]. Some studies have suggested that human immunodeficiency infection modifies the natural history of hepatitis C virus infection accelerating the progression of fibrosis and the development of cirrhosis [28, 29, 30, 31].

Co-infection HCV/HIV is very often discovered among injecting drug users [32, 33]. Thus, it was shown that about 90% drug users (consumers of heroin) are infected by hepatitis C virus [34]. Intravenous heroin abuse induces significant morphological changes in liver tissue (vesicular changes, fatty changes, chronic hepatitis, cirrhosis), and the severity of these changes increases with years of heroin abuse [35]. Authors supposed that worsening of morphological changes in the liver happens mostly often because of a significantly reduced detoxification functions of the liver.

Espinal, Peréz, Baéz, Hénriguez et al. [36] analyzed the clinical aspects of the co-infection HIV and tuberculosis. Tuberculosis remains an important public health problem in the world that has been exacerbated by HIV epidemic, resulting in increased morbidity and mortality [37, 38]. The pathogenesis and mechanisms of inflammation and accelerated fibrosis in co-infected patients are still poorly understood [28, 39].

At present investigation the peculiarities of patients with heroin abuse and co-infection (TB, HCV and HIV) were analyzed (see Table 1). All the patients were males of the age from 26 to 39 years (mean value was 32.2 years). The heroin abuse was the longest (mean value was 13.6 years). Patients with HCV-infection occupied the second position of disease duration (mean value was 7.1 years), than there were the patients with HIV-infection (mean value was 4.7 years) and finally the patients with TB-infection (mean value was 3.5 years). At last case the tuberculosis was discovered for the first time of 7 patients from 13 patients. It is characteristic that Mycobacterium tuberculosis was not discovered in phlegm of any patients under repeated analyses.

We could not detect any interconnections between the quantitative parameters of biopsy specimen getting with the use of computer microscopy and for the duration of above-mentioned observations.

Moreover the tendency to the diseases heaviness increasing is evident. The good example of this tendency is the biopsy specimen № 9: the duration of heroin abuse in this case composed 15 years, HIV – 13 years, TB – 12 years and HCV – 9 years. In accordance with it the cirrhosis developed in the liver of this patient (see Figure 6) and the segment of non-parenchymal elements reached 27.43%. Among them the specific part of portal zones was prevalent (27.16%).

The other peculiarity was the presence of the same stage of fibrosis (namely fibrosis F2 by METAVIR scoring) and F3 (by Ishak scoring) in liver of the majority of the patients.

At that time the segment of non-parenchyma elements in liver of these patients varied from 2.65% to 11.13%, and the specific part of the portal zones changed from 1.86% to 10.41%. The detailed information about discussion questions and interpretation of liver biopsy assessment by grading and staging systems was presented in recent works [40, 41].

The typical changes included the destruction of limiting plate, the expansion of portal areas and the development of interface hepatitis, formation of short septa or bridging necroses. The image analysis allows calculating of portal zones areas and intralobular infiltrates in different fields of biopsy vision. The expansion of portal zones took place especially during the development of interface hepatitis. As a rule, intensive lymphohistiocyte infiltration predominates in such a type of portal zones.

The region of intralobular infiltrates strongly varies. Our investigation showed that intralobular infiltrates developed as a result of lymphocyte-mediated death of hepatocytes (apoptosis).

Earlier we studied the apoptosis in liver biopsy specimens of the patients with HCV with the use of the TUNEL method [42, 43]. TUNEL-marked cells looked as small groups similar to intralobular piecemeal necroses. All morphometric parameters were significantly higher in comparison with monoinfection HCV [8].

5. Conclusion

Morphometric image analysis gives a possibility to evaluate quantitative parameters of necro-inflammatory and fibrosis changes in liver biopsy of patients with mixed infections and heroin abuse.

It is characteristic that the combination of different infections leads to the progression of liver inflammation and the increasing of the portion of non-parenchymal elements as a total sum of portal areas, intralobular infiltrates and distended hepatic vessels.

The investigation showed significant intensification of necroinflammatory lesions. Lymphohistiocyte infiltration was typical both for portal zones and intralobular areas. These morphological indications could be connected with the change of the immune state of patients as a result of combine effect of bacterial, viral infections and heroin abuse. So, numerous factors have been associated with an increased risk of fibrosis progression in liver of such type of patients.

Of course, it is necessary for more correct analysis to study the biopsies of the patients of several control groups with the sequential cut-off of the definite factors. We plan to carry out such investigation in future.

Quantitative analysis of digital images of total biopsies is indispensable to study the effectiveness of treatment tactics testing as the effect of therapy can be calculated as the percentage of morphological changes in biopsy.