Canadian Journal of Gastroenterology and Hepatology
Volume 2018 (2018), Article ID 3406789, 13 pages
https://doi.org/10.1155/2018/3406789

Review Article

Transient Elastography for Significant Liver Fibrosis and Cirrhosis in Chronic Hepatitis B: A Meta-Analysis

Xiaolong Qi,1,2 Min An,³ Tongwei Wu,² Deke Jiang,² Mengyun Peng,⁴ Weidong Wang,⁵ Jing Wang,⁴ Chunqing Zhang,¹ and on behalf of the CHESS Study Group²

¹Department of Gastroenterology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China
²CHESS, Hepatic Hemodynamic Lab, Institute of Hepatology, Nanfang Hospital, Southern Medical University, Guangdong Provincial Research Center for Liver Fibrosis, Guangzhou, China
³The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China
⁴Department of Hepatobiliary Disease, The Affiliated (T.C.M) Hospital of Southwest Medical University, Luzhou, China
⁵Department of Hepatobiliary Surgery, Shunde Hospital, Southern Medical University, Foshan, China

Correspondence should be addressed to Weidong Wang; wangweidong1968@126.com and Jing Wang; lywj68@126.com

Received 9 December 2017; Accepted 25 February 2018; Published 24 May 2018

Academic Editor: Mingyu Sun

Copyright © 2018 Xiaolong Qi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. The hepatitis B virus infection is a global health issue and the stage of liver fibrosis affects the prognosis in patients with chronic hepatitis B (CHB). We performed the meta-analysis describing diagnostic accuracy of transient elastography (TE) for predicting CHB-related fibrosis. Methods. We performed an adequate literature search to identify studies that assessed the diagnostic accuracy of TE in CHB patients using biopsy as reference standard. Hierarchical summary receiver-operating curves model and the bivariate mixed-effects binary regression model were applied to generate summary receiver-operating characteristic curves and pooled estimates of sensitivity and specificity. Results. The area under the summary receiver-operating curve for significant fibrosis and cirrhosis was 0.86 (95% confidence interval (CI): 0.83–0.89) and 0.92 (95% CI: 0.90–0.94), respectively. The sensitivity, specificity, and diagnostic odds ratio of TE for significant fibrosis were 0.78 (95% CI: 0.73–0.81, ; %), 0.81 (95% CI: 0.77–0.84, ; %), and 14.44 (95% CI: 10.80–19.31, ; %) and for cirrhosis were 0.84 (95% CI: 0.80–0.88, ; %), 0.87 (95% CI: 0.84–0.90, ; %), and 36.63 (95% CI: 25.38–52.87, ; %), respectively. The optimal cut-off values of TE were 7.25 kPa for diagnosing significant fibrosis and 12.4 kPa for diagnosing cirrhosis, respectively. Conclusion. TE is of great value in the detection of patients with CHB-related cirrhosis but has a suboptimal accuracy in the detection of significant fibrosis.

1. Introduction

Chronic hepatitis B virus infection continues to be a major public health issue worldwide with the prevalence of 3.61% [1]. As well known, liver fibrosis, one of the main prognostic factors in chronic hepatitis B (CHB), was associated with the risk of developing cirrhosis and cirrhosis-related complications [2, 3]. Therefore, liver fibrosis stage plays one of the most important roles in diagnostic and prognostic assessments in patients with CHB.

Liver biopsy (LB), as invasive in nature with related risks, is the gold standard for fibrosis assessment. However, LB is associated with obvious patient discomfort and risk of complications ranging from pain to more serious events with hospitalization rate of 1.4–3.2% [4] and mortality varying from 0.0088 to 0.3% [5]. Besides, LB provides only a quite small part of the organ, and thus there is a risk that the small part might not be representative for the live fibrosis in the whole liver [6].

Noninvasive methods of assessing fibrosis and cirrhosis were urgently needed, and serologic tests and novel imaging techniques were recently developed [7, 8]. Most of these studied focused on whether noninvasive methods can accurately detect minimal (F0-1), significant (≥F2), or advanced (≥F3-4) fibrosis based on the METAVIR score [9]. Transient elastography (TE), also known as FibroScan, was a device and a well-validated method with advantages of a short procedure time (<5 min), immediate results, and the ability to perform the test at the bedside or in an outpatient clinic [10]. Compared with blood tests, TE has a similar performance to predict significant fibrosis (SF) and higher accuracy to identify cirrhosis [11]. Measurement of liver fibrosis without biopsy is very tempting. In spite of the fact that recommendations suggested that noninvasive tests were still not ready to replace LB [12, 13], TE has become widely present in clinical practice. The accuracy of TE for detection of fibrosis has been assessed extensively in a variety of liver diseases [14–17]. However, it was reported that the presence of an IQR/M > 30% and liver stiffness median 7.1 kPa lead to a lower accuracy determined by the area under receiver-operating curve (AUROC) and these cases were considered “poorly reliable” [18]. Another study also indicated that there was a significant discrepancy in up to 20% of cases cirrhosis between different TE devices [19].

In the study, we performed an independent meta-analysis of the diagnostic accuracy of TE for predicting significant liver fibrosis (F2–4 versus F0-1) and cirrhosis (F4 versus F0–3) in CHB patients.

2. Methods

2.1. Literature Search Strategy

PubMed, Web of Science, and EMBASE database were searched to October 10, 2016, as well as Wanfang database and China National Knowledge Infrastructure. The search strategy was “FibroScan or transient elastography” in combination with “liver fibrosis assessment,” “significant fibrosis or cirrhosis or advanced liver fibrosis,” and “liver stiffness measurement.” All eligible studies were retrieved and their reference lists were checked for additional relevant publications.

2.2. Inclusion Criteria

All diagnostic cross-sectional studies, cohort studies, and randomized studies that compared TE accuracy with biopsy in diagnosis fibrosis grade were eligible for inclusion. Studies that met all the following criteria were included: (i) studies which reported that all patients had undergone biopsy and TE; (ii) having enough data to create 2 × 2 table of test performance (with numbers of true and false positives and negatives); and (iii) studies which reported the method of definition of the fibrosis grade.

2.3. Exclusion Criteria

The exclusion criteria were as follows: (i) the patients belonging to the pediatric population, hepatitis C/hepatitis B virus coinfected patients, mixed chronic liver disease patients (but not CHB and nonalcoholic fatty liver disease), and liver/kidney transplant patients; (ii) studies that were clearly extensions of previously published cohorts; and (iii) studies unable to obtain sufficient data for statistical analysis.

2.4. Methodological Assessment

Methodological quality was assessed by the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool. QUADAS-2 was designed to assess the internal and external validity. Any differences between two authors were resolved with discussion between the two review authors and the third author was final arbiter.

2.5. Data Extraction and Management

As for each study, the following information was extracted: year of publication, study design, sample size, presence of HIV coinfection, the QUADAS-2 methodological items, prevalence of each fibrosis stage on biopsy, along with total prevalence of SF and cirrhosis, interval between biopsy and TE, size of biopsy sample, type of scoring system used for histology (METAVIR versus other), and AUROC. Two authors performed the data extraction independently. Disagreement was resolved with discussion between the two review authors, with a third author as final arbiter.

2.6. Statistical Analysis and Data Synthesis

Initial analysis was performed with the Review Manager (RevMan) 5.0. Stata 12.0 was used for meta-analysis of diagnostic accuracy studies, to compute the pooled sensitivity and specificity and to plot the summary receiver-operating characteristics curve (SROC) with summary point and corresponding 95% confidence interval (CI). Regression analysis was performed by Stata 12.0, with each time point providing another covariate to verify the influence of the chosen covariate on the accuracy estimates. We used hierarchical SROC model and the bivariate random efforts model to produce SROC and pooled estimates of sensitivity and specificity. We performed Fagan test to detect clinical significant by Stata 12.0. Heterogeneity was assessed with the inconsistency index and values over 50% indicated substantial heterogeneity. Heterogeneity from threshold effect was explored by meta-disc 1.4.

3. Results

3.1. Search Results

1238 articles were obtained and 188 were excluded for duplicates. 882 were excluded based on title and abstracts, and full-text copies of 106 studies were obtained and assessed for eligibility. Furthermore, 62 were excluded for inappropriate methodology, duplicate sample, pediatric population, or inability to obtain data for at least 2 × 2 table. Finally, a total of 44 articles comprising 45 studies were enrolled in the meta-analysis (Figure 1).

Figure 1: Flow diagram of study selection process.

3.2. Characteristics of Included Studies

The overall prevalence of SF (F2–4) and cirrhosis (F4) ranged from 14.8% to 92.3% and from 1.1% to 69.2%, respectively. Reported AUROCs for SF diagnosis ranged from 0.614 to 0.98 (Table 1).

Table 1: Characteristics of the included studies.

Author
Study type
Year
HIV/HBV
METAVIR
Biopsy size
Biopsy to TE time (days)
Sample
Prevalence F2–F4
Prevalence F4
TE cut-off
AUROC

Cao et al.
Prospective
2014
NO
YES
>=15 mm and >=6 portal tracts
NA
162
0.61
0.12
7.3/17.5
NA/NA

Cardoso et al.
Retrospective
2011
NO
YES
>=15 mm and/or >=6 portal tracts
1
202
0.421
0.079
7.2/11
0.867/0.935

Castéra et al.
Prospective
2010
NO
YES
>=16 mm
NA
60
0.73
0.25
7.1/9.6
0.76/0.89

Chan et al.
Prospective
2009
NO
YES
>=15 mm and >=6 portal tracts
28
136
NA
0.25
NA/9
NA/0.93

Chen et al.
Retrospective
2011
NO
YES
>=15 mm
7
213
0.479
0.15
7.0/13.0
0.916/0.971

Chen et al.
Prospective
2012
NO
YES
>=15 mm and >=10 portal tracts
7
315
0.771
0.235
NA/10.4
NA/0.88

Cheng et al.
Prospective
2015
NO
YES
>=10 mm and >=8 portal tracts
1
459
0.61
0.152
7.2/18.2
0.82/0.87

Cheng et al.
Prospective
2014
NO
NO
>=15 mm and >=6 portal tracts
1
99
0.54
NA
8.15/NA
0.896/NA

Cho et al.
Prospective
2011
NO
YES
>=15 mm
1
121
0.727
0.074
7.8/14.0
0.849/0.867

Degos et al.
Prospective
2010
NO
YES
>=18 mm
1
284
0.415
0.102
5.2/12.9
0.78/0.90

Dong et al.
Prospective
2015
NO
NO
>=15 mm and >=6 portal tracts
NA
81
0.604
0.098
10.3/9.4
0.753/0.873

Gaia et al.
Prospective
2011
NO
YES
>=20 mm
120
70
0.53
0.31
7.2/10.6
0.674/0.763

Goyal et al.
Prospective
2013
NO
YES
>=15 mm and >=6 portal tracts
38
357
0.792
0.059
6.0/11.0
0.84/0.93

Huang et al.
Prospective
2016
NO
NO
>=15 mm
NA
263
0.148
0.011
8/NA
0.911/NA

Jia et al.
Prospective
2015
NO
YES
>=10 mm and >=8 portal tracts
NA
469
0.612
0.122
7.3/10.7
0.82/0.90

Kim et al. 1
Prospective
2012
NO
NO
>=20 mm
1
194
0.845
0.387
8.8/14.1
0.873/0.910

Kim et al. 2
Prospective
2012
NO
YES
>=20 mm
1
170
0.712
0.276
8.0/14.0
0.937/0.963

Kim et al.
Prospective
2009
NO
YES
>=10 mm and >=10 portal tracts
1
91
NA
0.692
NA/10.3
NA/0.803

Kim et al. 1
Prospective
2009
NO
YES
>=6 portal tracts
1
130
0.923
0.515
NA/10.1
NA/0.840

Kim et al. 2
Prospective
2009
NO
YES
>=15 mm
NA
91
0.868
0.396
NA/NA
0.837/0.913

Kim et al. 3
Prospective
2012
NO
NO
>=15 mm
1
150
0.847
0.453
6.0/9.4
NA/NA

Lesmana et al.
Retrospective
2011
NO
YES
>=15 mm and >=5 portal tracts
1
117
0.624
NA
5.85/NA
0.614/NA

liu et al.
Prospective
2015
NO
NO
>=8 portal tracts
NA
115
0.53
0.15
8.50/11.75
0.838/0.914

Liu et al.
Prospective
2012
NO
NO
>=10 mm
NA
134
0.43
0.11
7.60/13.20
0.93/0.96

Marcellin et al.
Prospective
2009
NO
YES
>=6 portal tracts
1
173
0.503
0.081
7.2/11.0
0.81/0.93

Meng et al.
Prospective
2015
NO
YES
>=12 mm and >=6 portal tracts
2
287
0.488
0.157
8.85/17.05
0.909/0.815

Meng et al.
Prospective
2016
NO
NO
>=15 mm
7
168
NA
0.15
15.1
0.927

Miailhes et al.
Prospective
2011
YES
YES
>=10 mm
3
59
0.61
0.203
5.9/9.4
0.85/0.96

Osakabe et al.
Prospective
2011
NO
YES
>=15 mm and >=8 portal tracts
30
51
0.882
0.275
7.1/16.0
0.844/0.93

Qin et al.
Prospective
2015
NO
NO
NA
1
152
0.68
0.07
8.2/13.1
0.752/0.973

Seo et al.
Retrospective
2015
NO
NO
>=15 mm
90
567
0.72
0.2
7.8/11.6
0.774/0.902

Sporea et al.
Prospective
2010
NO
YES
>=20 mm and >=8 portal tracts
NA
140
0.764
0.05
7/13.6
0.658/0.974

Stibbe et al.
Prospective
2011
NO
YES
>=20 mm
NA
48
0.458
0.104
7.0/14.0
NA/0.89

Trembling et al.
Prospective
2013
NO
YES
>=20 mm
1
182
0.626
0.198
NA/11.85
NA/O.95

Vigano et al.
Prospective
2011
NO
YES
>=20 mm
NA
125
0.53
0.16
6.2/13.1
NA/NA

Wang et al.
Prospective
2015
NO
NO
>=15 mm and >=6 portal tracts
NA
142
0.585
0.092
8.15/13.95
0.897/0.968

Wang et al.
Prospective
2014
NO
NO
>=15 mm
NA
80
0.7
0.1125
7.3/12.4
0.865/0.944

Wang et al.
Prospective
2016
NO
NO
NA
NA
127
0.76
0.24
NA/15.2
NA/0.805

Wong et al.
Prospective
2009
NO
YES
>=15 mm and >=6 portal tracts
NA
134
0.78
0.24
NA/13.4
NA/0.89

Wong et al. Tr-c
Prospective
2014
NO
YES
>=15 mm and >=6 portal tracts
NA
238
0.693
0.235
NA/10
NA/0.9

Wong et al. Va-c
Prospective
2014
NO
YES
>=15 mm and >=6 portal tracts
NA
85
0.565
0.259
NA/10
NA/0.87

Zhang et al.
Prospective
2016
NO
NO
>=22 mm
7
180
0.72
0.18
7.5/10.6
0.813/0.799

Zhang et al.
Prospective
2016
NO
NO
>=15 mm
NA
124
0.54
NA
6.95
0.732

Zhang et al.
Prospective
2011
NO
NO
>=15 mm and >=6 portal tracts
NA
88
0.671
0.159
7.25/12.40
0.857/0/948

Zhu et al.
Prospective
2011
NO
YES
>=15 mm and >=6 portal tracts
1
175
NA
0.166
7.9/13.8
NA/0.98

AUROC, area under the receiver-operating curve; TE, transient elastography; HIV/HBV, hepatitis B and HIV-coinfected patients; METAVIR, liver biopsy assessed according to METAVIR or not; TE cut-off, TE cut-off used to predict; NA, data not available.

As shown in Table 1, only Miailhes et al. reported HIV coinfected patients [20]. In sixteen studies , LB was assessed with a histological score other than METAVIR [21–36]. In eight studies , mean length of biopsy sample was ≥20 mm [22, 34, 37–42]. Besides, in nineteen studies , data on time interval between biopsy and TE were not obtained [11, 21, 23, 25, 27, 28, 32–34, 39, 40, 42–47]. Three studies did not report cirrhosis (F4) [24, 35, 48]. Only four studies were retrospective [31, 48–50].

As presented in Figure 2, the results of methodological quality assessment based on the QUADAS-2 scale were depicted for all of the 44 eligible studies. The majority of the methodological concern lies within the index test, because TE in ten studies interpreted with knowledge of the results of the biopsy [24, 29, 33, 39, 46, 48, 51–54] and TE in one study was conducted with assistance by a time-motion ultrasound image [40]. Another possible issue was addressed in patient selection that participants might be enrolled consecutively with confirmed diagnosis in three studies [31, 50, 55]. Both of these concerns might be located in heterogeneity and sensitivity analyses.

(a)

(b)

Figure 2: Summary of methodological quality of 44 studies according to Quality Assessment of Diagnostic Studies-2 (QUDAS-2) tool. (a) Overall and (b) study-level of bias.

3.3. Diagnosis of SF

We included 35 studies ( = 6,202) in the analysis for SF (F2–F4) [15–23, 25–27, 29–35, 37–40, 43, 56–59]. Summary representation of the overall analysis was presented in Figure 3(a) and Supplementary Figure 1. Sensitivity and specificity ranged from 51 to 97% and 38 to 100%, respectively (Supplementary Figure 1).

(a)

(b)

(c)

Figure 3: Meta-analysis of 32 studies that assessed the diagnosis accuracy of significant fibrosis based on transient elastography. (a) A summary receiver-operating characteristic (SROC) plot of transient elastography for detection of significant liver fibrosis (METAVIR F2–F4). (b) Regression analysis of studies whether reported with METAVIR score on the next day of biopsy or with sample size ≥ 20 cm for significant liver fibrosis. (c) Detection of clinical significance for significant liver fibrosis (METAVIR F2–F4) based on Fagan test. Heterogeneity was generated if in sensitivity or specificity separately. However, joint value was generated synthesisly for analysis of both sensitivity and specificity.

The area under SROC for SF was 0.86 (95% CI: 0.83–0.89) (Figure 3(a)). The meta-analysis summary estimate indicated pooled sensitivity of 0.78 (95% CI: 0.73–0.81, ; ), specificity of 0.81 (95% CI: 0.77–0.84, ; %) (Supplementary Figure 1(A)), positive likelihood ratio (LR+) of 4.01 (95% CI: 3.31–4.84, ; %), negative likelihood ratio (LR−) of 0.28 (95% CI: 0.23–0.33, ; %) (Supplementary Figure 1(B)), diagnostic score (DS) of 2.67 (95% CI: 2.38–2.96, ; %), and diagnostic odds ratio (DOR) of 14.44 (95% CI: 10.80–19.30, ; %) (Supplementary Figure 1(C)). However, it must be carefully considered as they were not pooled from studies with identical TE threshold. Overall, there was heterogeneity as graphically illustrated on the forest plot in Supplementary Figure 1. The cut-off value for SF (F2–4) ranged from 5.2 to 10.3 kPa with a mean value of 8.6 kPa and a median of 7.25 kPa.

As shown in Figure 3(b) and Table 2, in the analysis of LB-related factors with an impact on accuracy, there was no significant difference (joint for classification criteria; joint for interval time; joint for average sample size). 26 studies conducted in Asian presented a better both pooled sensitivity (0.78, 95% CI: 0.73–0.82) and specificity (0.83, 95% CI: 0.79–0.87) than in Caucasian (joint ).

Table 2: Results of meta-regression for significant fibrosis.

Covariate
Number
Pooled sensitivity
value
Pooled specificity
value
Joint value

Classification criteria

METAVIR score
21
0.78 (0.75–0.83)
<0.01
0.79 (0.73–0.84)
<0.01
0.47

Non-METAVIR score
14
0.77 (0.70–0.83)
0.83 (0.78–0.89)

Interval time

On the next day of liver biopsy
11
0.76 (0.69–0.84)
<0.01
0.85 (0.79–0.90)
<0.01
0.29

More than one day after liver biopsy
24
0.78 (0.73–0.83)
0.78 (0.74–0.83)

Average sample size

⩾20 mm
7
0.76 (0.66–0.86)
<0.01
0.79 (0.69–0.88)
<0.01
0.77

Not ⩾ 20 mm
28
0.78 (0.74–0.82)
0.81 (0.77–0.85)

Region

Asian
26
0.78 (0.73–0.82)
<0.01
0.83 (0.79–0.87)
0.04
0.03

Caucasian
9
0.77 (0.68–0.85)
0.72 (0.63–0.80)

As presented in Figure 3(c), it was indicated that posttest probability of LR+ increased to 86% and LR− decreased to 29% after TE was performed based on Fagan test.

3.4. Diagnosis of Cirrhosis

41 studies were included in the cirrhotic analysis with a total of 7,205 patients, as four studies did not have any cases of liver cirrhosis (METAVIR F4) [21, 24, 35, 48]. The overall prevalence of METAVIR F4 and the AUROCs in the included studies ranged from 5% to 69.2% and from 0.80 to 0.98 (Table 1), respectively.

Summary representation of the overall analysis was shown in Figure 4(a). The area under the SROC for liver cirrhosis was 0.92 (95% CI: 0.90–0.94). Sensitivity ranged from 49% to 100%, much more widely than specificity which ranged from 62% to 99% (Supplementary Figure 2). The meta-analysis summary estimate covered the pooled sensitivity of 0.84 (95% CI: 0.80–0.88, ; %), specificity of 0.87 (95% CI: 0.84–0.90, ; %) (Supplementary Figure 2(A)), LR+ of 6.66 (95% CI: 5.34–8.31, ; %), LR− of 0.18 (95% CI: 0.14–0.23, ; %) (Supplementary Figure 2(B)), DS of 3.60 (95% CI: 3.23–3.97, ; %), and DOR of 36.63 (95% CI: 25.38–52.87, ; %), respectively (Supplementary Figure 2(C)). Again, these measures must be carefully considered without identical TE thresholds. The cut-off value for cirrhosis ranged from 9 kPa to 18.2 kPa with both a mean value and a median of 12.4 kPa.

(a)

(b)

(c)

Figure 4: Meta-analysis of 37 studies that assessed the diagnosis accuracy of cirrhosis based on transient elastography. (a) A summary receiver-operating characteristic (SROC) plot of transient elastography for detection of cirrhosis (METAVIR F4). (b) Regression analysis of studies whether reported with METAVIR score on the next day of biopsy or with sample size ≥ 20 cm for cirrhosis. (c) Detection of clinical significance for cirrhosis (METAVIR F4) based on Fagan test.

As shown in Figure 4(b) and Table 3, although summary sensitivity was lower and summary specificity was higher in studies with METAVIR score (sensitivity: 0.82, 95% CI: 0.77–0.87; specificity: 0.88, 95% CI: 0.85–0.91), TE performed on the next day of LB (sensitivity: 0.79, 95% CI: 0.71–0.86; specificity: 0.88, 95% CI: 0.84–0.93), and average sample length 20 mm (sensitivity: 0.79, 95% CI: 0.69–0.89; specificity: 0.88, 95% CI: 0.83–0.94), respectively, no statistical significance was detected (joint for classification criteria; joint for interval time; joint for average sample size). Besides, pooled sensitivity and specificity were without significant difference (joint ) between Caucasian (sensitivity: 0.78, 95% CI: 0.67–0.88; specificity: 0.91, 95% CI: 0.86–0.95) and Asian (sensitivity: 0.86, 95% CI: 0.81–0.90; specificity: 0.86, 95% CI: 0.83–0.89).

Table 3: Results of meta-regression for cirrhosis.

Covariate
Number
Pooled sensitivity
value
Pooled specificity
value
Joint value

Classification criteria

METAVIR score
28
0.82 (0.77–0.87)
<0.01
0.88 (0.85–0.91)
<0.01

0.17

Non-METAVIR score
13
0.89 (0.83–0.94)
0.86 (0.80–0.91)

Interval time

On the next day of liver biopsy
13
0.79 (0.71–0.86)
<0.01
0.88 (0.84–0.93)
<0.01

0.21

More than one day after liver biopsy
28
0.86 (0.82–0.90)
0.87 (0.83–0.90)

Average sample size

⩾20 mm
8
0.79 (0.69–0.89)
<0.01
0.88 (0.83–0.94)
<0.01

0.47

Not ⩾ 20 mm
33
0.85 (0.81–0.89)
0.87 (0.84–0.90)

Region

Asian
31
0.86 (0.81–0.90)
<0.01
0.86 (0.83–0.89)
<0.01

0.12

Caucasian
10
0.78 (0.67–0.88)
0.91 (0.86–0.95)

In addition, based on Fagan test, it was illustrated that posttest probability of LR+ and LR− rose and declined to 59% and 4%, respectively (Figure 4(c)).

3.5. Publication Bias

The results of publication bias analysis were performed with Stata in Supplementary Figure 3. No significant publication bias was detected according to Deeks figures for SF . However, there was bias among 41 studies enrolled in analysis of TE for cirrhosis , which might result from the positive results of all 41 studies.

4. Discussion

TE can provide a reliable detection of liver fibrosis in patients with CHB and thus has been recommended by the American Association for the Study of Liver Diseases (AASLD) and European Association for the Study of the Liver (EASL) [60, 61]. This meta-analysis was conducted in a total of 7,808 CHB patients to summarize the diagnostic accuracy of TE for CHB-related SF, with optimal statistical method SROC. In addition, regression analysis was carried out to further explore sources of heterogeneity.

In our study, TE performed well in both SF (F2–4) and cirrhosis (F4) with pooled sensitivity of 78% and 84%, summary specificity of 81% and 87%, DOR of 14.44 and 36.63, LR+ of 4.01 and 6.66, LR− of 0.28 and 0.18, respectively. Study by Li et al. [62] with hierarchical SROC model was also performed in CHB patients, with summary sensitivity and specificity for SF (F2–4) and cirrhosis (F4) of 80% and 86%, 82%, and 88%, however, without DOR, LR+ and LR−. Interestingly, the pooled specificity for diagnosis SF (F2–4) and cirrhosis (F4) in both studies were higher than summary sensitivity, which suggested that the currently cut-off values of TE performed better in excluding diseases rather than confirming diseases. Furthermore, the areas under the SROC were 0.86 for SF (F2–4) and 0.92 for cirrhosis (F4), respectively, which indicated that TE was performed well in staging fibrosis in CHB patients. In addition, TE performed better for cirrhosis than SF with a higher value of AUC, sensitivity, specificity, DOR, LR+, and a lower value of LR−. Although the diagnostic accuracy was higher for cirrhosis, TE could also increase the diagnostic accuracy for SF based on Fagan test with increased LR+ and decreased LR−.

The higher TE values were used to confirm diagnosis, while the lower one was used to exclude the false positive diagnosis. However, if the TE value located between the values for rule in and rule out, biopsy was then recommended. Based on the descriptive statistics of enrolled studies, the cut-off values for diagnosing SF (F2–4) and cirrhosis (F4) ranged from 5.2 to 10.3 kPa and 9 to 18.2 kPa, respectively. The optimal cut-off values of TE in CHB patients in our study were 7.25 kPa for SF (F2–4) and 12.4 kPa for cirrhosis (F4). In the previous meta-analysis by Li et al., the weighted mean cut-off values of TE were comparable with 7.2 kPa for SF (F2-4) and 12.2 kPa for cirrhosis (F4) [62]. However, since there was no optimal statistical method to pool different cut-off values in individual studies, the optimal cut-off values in our meta-analysis were simply summarized as median, which could eliminate the impact resulting from the maximum and minimum values that was better than the mean value in previous study [62].

Elevated ALT levels might affect the predictive accuracy of TE [16, 24, 45, 50, 55, 56]; however, the study by Cardoso et al. reported that the use of TE cut-off values adjusted to ALT level did not improve the performance of liver stiffness in CHB patients [49]. Although elevated ALT might be the most important confounder on liver stiffness measurement, the synthesis analysis of ALT elevation could not be conducted due to insufficient data. Therefore, it would be beneficial if more clinical studies focused on the correlation between ALT elevation and TE in CHB patients.

One of the main limitations in this meta-analysis was the significant heterogeneity of the included studies. Spearman correlation coefficient for SF and cirrhosis were 0.055 and 0.057 , and no threshold effect was presented. Therefore, regression analysis was carried out. Besides, TE value could be applied as diagnosis criteria for both SF and cirrhosis in Asian. However, for Caucasian, it was noted that TE was valid to diagnosis of cirrhosis, while it was less precise for SF. Unfortunately, the regression analysis was not conducted owing to the small size of HIV- and non-HIV-coinfected patients. It should be noted that the overlapped cut-off values from included studies might also result in the heterogeneity.

In conclusion, TE is of great value for detection CHB-related cirrhosis, however, with a suboptimal performance in detection of SF. Further studies should focus on the TE cut-off value and the effect of ALT elevation in patients with CHB.

Abbreviations

CHB: | Chronic hepatitis B
CI: | Confidence interval
DOR: | Diagnostic odds ratio
LB: | Liver biopsy
LR: | Likelihood ratio
QUADAS-2: | Quality Assessment of Diagnostic Accuracy Studies-2
SF: | Significant fibrosis
SROC: | Summary receiver-operating curves
TE: | Transient elastography
AUROC: | Area under receiver-operating curve.

Conflicts of Interest

The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patients received or pending, or royalties.

Authors’ Contributions

Xiaolong Qi, Weidong Wang, Jing Wang, and CHESS Study Group contributed to study concepts and design; Min An and Tongwei Wu performed literature search; Min An and Jing Wang conducted data extraction; Min An, Tongwei Wu, Deke Jiang, Mengyun Peng, and Chunqing Zhang performed data analysis: Tongwei Wu, Weidong Wang, Chunqing Zhang, and CHESS Study Group were responsible for manuscript preparation and revision. All authors and CHESS Study Group have participated sufficiently in the study and approved the final version. Xiaolong Qi, Min An, and Tongwei Wu contributed equally to this work.

Acknowledgments

Collaborators of CHESS Study Group are as follows: Zhiwei Li, Department of General Surgery, 302 Hospital of PLA, Beijing, China; Fuquan Liu, Department of Interventional Therapy, Beijing Shijitan Hospital, Capital Medical University, Beijing, China; Guofeng Chen, Liver Cirrhosis Diagnosis and Treatment Center, 302 Hospital of PLA, Beijing, China; and Qingge Zhang, Department of Hepatology, Xingtai People’s Hospital, Xingtai, China. This work was supported by the grants from the National Natural Science Foundation of China (81600510), Guangzhou Industry-Academia-Research Collaborative Innovation Major Project (201704020015), and President Foundation of Nanfang Hospital, Southern Medical University (2017Z012).

Supplementary Materials

Supplementary Figure 1: meta-analysis of 32 studies that assessed the diagnosis accuracy of significant fibrosis (METAVIR F2–F4) based on transient elastography. A Forest plot of (A) sensitivity and specificity, (B) positive and negative likelihood ratio, and (C) diagnostic score (DS) and diagnostic odds ratio (DOR) for significant liver fibrosis (METAVIR F2–F4). Supplementary Figure 2: meta-analysis of 37 studies that assessed the diagnosis accuracy of cirrhosis (METAVIR F4) based on transient elastography. A Forest plot of (A) sensitivity and specificity, (B) positive and negative likelihood ratio, and (C) DS and DOR for cirrhosis (METAVIR F4). Supplementary Figure 3: Deeks’ Funnel Plot Asymmetry Test for (A) significant fibrosis (METAVIR F2–F4) and (B) cirrhosis (METAVIR F4). (Supplementary Materials)

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