Systematic review and individual-patient-data meta-analysis of non-invasive fibrosis markers for chronic hepatitis B in Africa

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Johannessen, Asgeir | Stockdale, Alexander | Henrion, Marc | Okeke, Edith | Seydi, Moussa | Wandeler, Gilles | Sonderup, Mark | Spearman, C. Wendy | Vinikoor, Michael | Sinkala, Edford | Desalegn, Hailemichael | Fall, Fatou | Riches, Nicholas | Davwar, Pantong | Duguru, Mary | Maponga, Tongai | Taljaard, Jantjie | Matthews, Philippa | Andersson, Monique | Mboup, Souleyman | Sombie, Roger | Shimakawa, Yusuke | Lemoine, Maud

Edité par CCSD ; Nature Publishing Group -

International audience. In sub-Saharan Africa, simple biomarkers of liver fibrosis are needed to scale-up hepatitis B treatment. We conducted an individual participant data meta-analysis of 3,548 chronic hepatitis B patients living in eight sub-Saharan African countries to assess the World Health Organization-recommended aspartate aminotransferase-to-platelet ratio index and two other fibrosis biomarkers using a Bayesian bivariate model. Transient elastography was used as a reference test with liver stiffness measurement thresholds at 7.9 and 12.2kPa indicating significant fibrosis and cirrhosis, respectively. At the World Health Organization-recommended cirrhosis threshold (>2.0), aspartate aminotransferase-to-platelet ratio index had sensitivity (95% credible interval) of only 16.5% (12.5–20.5). We identified an optimised aspartate aminotransferase-to-platelet ratio index rule-in threshold (>0.65) for liver stiffness measurement >12.2kPa with sensitivity and specificity of 56.2% (50.5–62.2) and 90.0% (89.0–91.0), and an optimised rule-out threshold (<0.36) with sensitivity and specificity of 80.6% (76.1–85.1) and 64.3% (62.8–65.8). Here we show that the World Health Organization-recommended aspartate aminotransferase-to-platelet ratio index threshold is inappropriately high in sub-Saharan Africa; improved rule-in and rule-out thresholds can optimise treatment recommendations in this setting.

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