Diagnostic accuracy of non-invasive tests for advanced fibrosis in patients with NAFLD: an individual patient data meta-analysis

被引:338
作者
Mozes, Ferenc Emil [1 ]
Lee, Jenny A. [2 ]
Selvaraj, Emmanuel Anandraj [1 ,3 ,4 ,5 ]
Jayaswal, Arjun Narayan Ajmer [1 ]
Trauner, Michael [6 ]
Boursier, Jerome [7 ,8 ]
Fournier, Celine [9 ]
Staufer, Katharina [6 ,10 ,11 ]
Stauber, Rudolf E. [12 ]
Bugianesi, Elisabetta [13 ]
Younes, Ramy [14 ]
Gaia, Silvia [13 ]
Lupsor-Platon, Monica [15 ]
Petta, Salvatore [16 ]
Shima, Toshihide [17 ]
Okanoue, Takeshi [17 ]
Mahadeva, Sanjiv [18 ]
Chan, Wah-Kheong [18 ]
Eddowes, Peter J. [19 ,20 ]
Hirschfield, Gideon M. [21 ]
Newsome, Philip Noel [19 ,22 ,23 ]
Wong, Vincent Wai-Sun [24 ]
de Ledinghen, Victor [25 ,26 ]
Fan, Jiangao [27 ]
Shen, Feng [27 ]
Cobbold, Jeremy F. [3 ,4 ,5 ]
Sumida, Yoshio [28 ]
Okajima, Akira [29 ]
Schattenberg, Joern M. [30 ]
Labenz, Christian [30 ]
Kim, Won [31 ]
Lee, Myoung Seok [32 ]
Wiegand, Johannes [33 ]
Karlas, Thomas [33 ]
Yilmaz, Yusuf [34 ,35 ]
Aithal, Guruprasad Padur [20 ,36 ]
Palaniyappan, Naaventhan [20 ,36 ]
Cassinotto, Christophe [37 ]
Aggarwal, Sandeep [38 ]
Garg, Harshit [38 ]
Ooi, Geraldine J. [39 ]
Nakajima, Atsushi [40 ]
Yoneda, Masato [40 ]
Ziol, Marianne [41 ,42 ]
Barget, Nathalie [43 ]
Geier, Andreas [44 ]
Tuthill, Theresa [45 ]
Brosnan, M. Julia [45 ]
Anstee, Quentin Mark [46 ]
Neubauer, Stefan [1 ]
机构
[1] Univ Oxford, Radcliffe Dept Med, Cardiovasc Med, Oxford, Oxon, England
[2] Univ Amsterdam, Dept Epidemiol & Data Sci, Amsterdam UMC, Amsterdam, Netherlands
[3] Univ Oxford, Translat Gastroenterol Unit, Oxford, England
[4] Oxford Univ Hosp NHS Fdn Trust, NIHR Oxford Biomed Res Ctr, Oxford, England
[5] Univ Oxford, Oxford, England
[6] Med Univ Vienna, Dept Med 3, Div Gastroenterol & Hepatol, Vienna, Austria
[7] Univ Angers, Lab HIFIH, UPRES EA 3859, SFR ICAT 4208, Angers, Pays De La Loir, France
[8] Ctr Hosp Univ Angers, Serv Hepatogastroenterol & Oncol Digest, Angers, Pays De La Loir, France
[9] Echosens SA, Paris, Ile De France, France
[10] Inselspital Univ Hosp Bern, Dept Visceral Surg & Med, Bern, Switzerland
[11] Med Univ Vienna, Dept Surg, Div Transplantat, Vienna, Austria
[12] Med Univ Graz, Dept Internal Med, Graz, Austria
[13] Univ Turin, Med Sci, Turin, Italy
[14] Boehringer Ingelheim Int GmbH, Ingelheim, Rheinland Pfalz, Germany
[15] Univ Med & Pharm, Reg Inst Gastroenterol & Hepatol Prof Dr Octavian, Dept Ultrasonog, Cluj Napoca, Romania
[16] PROMISE, Sect Gastroenterol & Hepatol, Palermo, Italy
[17] Saiseikai Suita Hosp, Hepatol Ctr, Suita, Osaka, Japan
[18] Univ Malaya, Fac Med, Dept Med, Kuala Lumpur, Wilayah Perseku, Malaysia
[19] Univ Birmingham, NIHR Biomed Res Ctr, Birmingham, W Midlands, England
[20] Univ Nottingham, NIHR Nottingham Biomed Res Ctr, Nottingham, England
[21] Univ Hlth Network, Toronto Ctr Liver Dis, Toronto, ON, Canada
[22] Univ Birmingham, Inst Immunol & Immunotherapy, Ctr Liver & Gastrointestinal Res, Birmingham, W Midlands, England
[23] Univ Hosp Birmingham NHS Fdn Trust, Liver Unit, Birmingham, W Midlands, England
[24] Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Peoples R China
[25] Hop Haut Leveque, Ctr Invest Fibrose Hepat, Pessac, France
[26] Univ Bordeaux, INSERM 1053, Talence, Aquitaine, France
[27] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Gastroenterol, Sch Med, Shanghai, Peoples R China
[28] Aichi Med Univ, Dept Internal Med, Nagakute, Aichi, Japan
[29] Koseikai Takeda Hosp, Dept Gastroenterol, Kyoto, Japan
[30] Johannes Gutenberg Univ Mainz, Dept Internal Med 1, Rhineland Palatinate, Univ Med Ctr, Mainz, Rhineland Palat, Germany
[31] Seoul Natl Univ, Seoul Metropolitan Govt Boramae Med Ctr, Dept Gastroenterol & Hepatol, Dept Internal Med,Coll Med, Seoul, South Korea
[32] Seoul Natl Univ, Dept Radiol, Seoul Metropolitan Govt Boramae Med Ctr, Seoul, South Korea
[33] Leipzig Univ Med Ctr, Dept Med 2, Leipzig, Sachsen, Germany
[34] Marmara Univ, Dept Gastroenterol, Sch Med, Istanbul, Turkey
[35] Marmara Univ, Inst Gastroenterol, Istanbul, Turkey
[36] Univ Nottingham, Nottingham Digest Dis Ctr, Sch Med, Nottingham, England
[37] Univ Hosp Ctr Montpellier, Diagnost & Intervent Radiol, Montpellier, Languedoc Rouss, France
[38] AIIMS, Dept Surg Disciplines, Delhi, India
[39] Monash Univ, Dept Surg, Prahran, Vic, Australia
[40] Yokohama City Univ, Dept Gastroenterol & Hepatol, Yokohama, Kanagawa, Japan
[41] Hop Jean Verdier, Serv Anat Pathol, Paris, France
[42] Hop Jean Verdier, Ctr Ressources Biol, Paris, France
[43] Hop Univ Paris Seine St Denis, Ctr Ressources Biol, Bondy, Ile De France, France
[44] Univ Hosp Wurzburg, Div Hepatol, Wurzburg, Bayern, Germany
[45] Pfizer Inc, Internal Med Res Unit, Cambridge, MA USA
[46] Newcastle Univ, Fac Med, Translat & Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
基金
欧盟地平线“2020”;
关键词
hepatic fibrosis; fatty liver; clinical decision making; biostatistics; LIVER STIFFNESS MEASUREMENT; CONTROLLED ATTENUATION PARAMETER; TRANSIENT ELASTOGRAPHY; XL PROBE; NONALCOHOLIC STEATOHEPATITIS; PROSPECTIVE DERIVATION; CHRONIC HEPATITIS; DISEASE; SCORE; BIOPSY;
D O I
10.1136/gutjnl-2021-324243
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Liver biopsy is still needed for fibrosis staging in many patients with non-alcoholic fatty liver disease. The aims of this study were to evaluate the individual diagnostic performance of liver stiffness measurement by vibration controlled transient elastography (LSM-VCTE), Fibrosis-4 Index (FIB-4) and NAFLD (non-alcoholic fatty liver disease) Fibrosis Score (NFS) and to derive diagnostic strategies that could reduce the need for liver biopsies. Design Individual patient data meta-analysis of studies evaluating LSM-VCTE against liver histology was conducted. FIB-4 and NFS were computed where possible. Sensitivity, specificity and area under the receiver operating curve (AUROC) were calculated. Biomarkers were assessed individually and in sequential combinations. Results Data were included from 37 primary studies (n=5735; 45% women; median age: 54 years; median body mass index: 30 kg/m(2); 33% had type 2 diabetes; 30% had advanced fibrosis). AUROCs of individual LSM-VCTE, FIB-4 and NFS for advanced fibrosis were 0.85, 0.76 and 0.73. Sequential combination of FIB-4 cut-offs (<1.3; >= 2.67) followed by LSM-VCTE cut-offs (<8.0; >= 10.0 kPa) to rule-in or rule-out advanced fibrosis had sensitivity and specificity (95% CI) of 66% (63-68) and 86% (84-87) with 33% needing a biopsy to establish a final diagnosis. FIB-4 cut-offs (<1.3; >= 3.48) followed by LSM cut-offs (<8.0; >= 20.0 kPa) to rule out advanced fibrosis or rule in cirrhosis had a sensitivity of 38% (37-39) and specificity of 90% (89-91) with 19% needing biopsy. Conclusion Sequential combinations of markers with a lower cut-off to rule-out advanced fibrosis and a higher cut-off to rule-in cirrhosis can reduce the need for liver biopsies.
引用
收藏
页码:1006 / 1019
页数:14
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