Facteurs Associés à la Fibrose Hépatique au Cours de la Stéatopathie Métabolique à Abidjan
Fibrose hépatique pendant la stéatopathie métabolique à Abidjan
DOI:
https://doi.org/10.5281/hra.v2i3.5409Keywords:
NAFLD, NASH, impulse elastometry, steatosis, fibrosis, AbidjanAbstract
RÉSUMÉ
Introduction. Le faible nombre d’études sur les facteurs de risque de la fibrose hépatique dans la stéatopathie métabolique (NAFLD) en Afrique subsaharienne nous a conduit à initier ce travail dont le but était de déterminer les facteurs associés à la fibrose hépatique au cours de la NAFLD diagnostiquée par l’élastométrie impulsionnelle (Fibroscan©) chez le noir africain. Méthodes. Nous avons inclus 51 patients recrutés au sein du CHU de Cocody et au siège de la Société Générale des Banques de Côte d’Ivoire dans la ville d’Abidjan. Tous les patients ont effectué un Fibroscan®. Il existait une fibrose significative lorsque F>=2. La stéatose était présente si S >215dB/m. Les tests de Chi 2 et de la régression logistique ont été utilisés. Ils étaient significatifs lorsque p<0,05. Résultats. La NASH était présente chez 54,1% (n=28), la NAFL chez 46,9% (n=23). 58,7% des patients NAFLD (n=30) avaient une fibrose significative. 96 % des patients avaient un IMC ≥ 25kg/m². 56,9% des patients présentaient une stéatose modérée à sévère. Les facteurs de risque associés à la survenue de fibrose significative en analyse uni variée étaient : le sexe masculin, l’âge supérieur à 40 ans, le surpoids, l’obésité, les grades de stéatose légère et modérée, l’obésité tronculaire et le cholestérol total. L’obésité tronculaire était le seul facteur indépendamment associé à la survenue de la fibrose hépatique en analyse multi variée. Conclusion. L’obésité est le principal facteur de risque de survenue de fibrose et de stéatose chez les patients NAFLD.
ABSTRACT
Introduction. Metabolic steatopathy (NAFLD) is the hepatic manifestation of metabolic syndrome. The low number of studies on the evaluation of fibrosis in sub-Saharan black Africa led us to initiate this work, the aim of which was to determine the factors associated with fibrosis in course of NAFLD diagnosed by impulse elastometry (Fibroscan©) in black African subjects. Methods. We included 51 patients recruited within the Cocody University Hospital and at the headquarters of the Société Générale des Banques de Côte d'Ivoire in the city of Abidjan. All patients underwent a Fibroscan®. There was significant fibrosis when F>=2. Steatosis was present if S >215dB/m. Chi square and logistic regression tests were used. They were significant when p<0.05. Results. NASH was present in 54.1% (n=28), NAFL in 46.9% (n=23). 58.7% of NAFLD patients (n=30) had significant fibrosis with a predominance for NASH patients. 96% of patients had a BMI ≥ 25kg/m². 56.9% of patients presented moderate to severe steatosis. The risk factors associated with the occurrence of significant fibrosis in univariate analysis were: male sex, age over 40 years, overweight, obesity, grades of mild and moderate steatosis, truncal obesity and total cholesterol. Truncal obesity was the only factor independently associated with the occurrence of hepatic fibrosis in multivariate analysis. Conclusion. Impulse elastometry (Fibroscan®) is a non-invasive method for assessing and stratifying hepatic fibrosis and steatosis. Obesity is the main risk factor for the occurrence of fibrosis and steatosis in NAFLD patients.
References
LaBrecque D, Abbas Z, Annania F. Stéatose hépatique et stéato-hépatite non alcoolique. World Gastroenterology Organisation Global Guidelines 2012.
Younossi ZM, Koenig AB, Abdelatif D, et al. Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology 2016;64:73-84
Perumpail BJ, Khan MA, Yoo ER. Clinical epidemiology and diseases burden of nonalcoholic fatty liver disease. World J Gastroenterol 2017; 23(47):8263-76.
De Ledinghen V, Vergniol J, Foucher J. Non-invasive diagnosis of liver steatosis using controlled attenuation parameter (CAP) and transient elastography. Liver Int. 2012;32(6):911-18
Vallet-Pichard A, Parlati L, Stanislas P. Épidémiologie de la stéato-hépatite non alcoolique. Étendue du problème et son impact sur la santé publique. Presse Med.(2019)
Organisation mondiale de la Santé – Profils des pays pour le diabète, 2016. http://origin.who.int/diabetes/country-profiles/civ_fr.pdf
Sasso M, Beaugrand,M, de Ledinghe V, Controlled attenuation parameter (CAP): a novel VCTE™ guided ultrasonic attenuation measurement for the evaluation of hepatic steatosis: preliminary study and validation in a cohort of patients with chronic liver disease from various cause. Ultrasound Med Bio. 2010 Nov;36(11):1825-35.
Fonkoua S. Memoire; Facteur de risque métabolique chez le sujet noir africain
R. Ntagirabiri · J. Cikomola · E. Baransaka, Stéatose hépatique lors du syndrome métabolique chez l’adulte noir africain: cas du Burundi J. Afr. Hépatol. Gastroentérol.Dec;2014 /1-4
Tran A, Gelaye B, Girma B. Prevalence of metabolic syndrome among working adults in Ethiopia. Int J Hypertens 2011;2011:193719
Sodjinou R, Agueh V, Fayomi B. Obesity and cardiometabolic risk factors in urban adults of Benin: Relationship with socio-economic status, urbanisation, and lifestyle Patterns. BMC Public Health 2008;8:84
Kawamura Y, Arase Y, Ikeda K. Large-scale long-term follow-up study of Japanese patients with nonalcoholic fatty liver disease for the onset of hepatocellular carcinoma. Am J Gastroenterol 2012;107(2):253-61.
Madan K, Batra Y, Gupta SD. Nonalcoholic fatty liver disease may not be a severe disease at presentation among Asian Indians. World J Gastroenterol 2006;12(21):3400-405.
Francque S, De Maeght S, Adler M. High prevalence of advanced fibrosis in association with the metabolic syndrome in a Belgian prospective cohort of NAFLD patients with elevated ALT. Results of the Belgian NAFLD registry. Acta Gastroenterol Belg 2011;74(1):9-16.
Margariti A, Deutsch M, Manolakopoulos S. The severity of histologic liver lesions is independent of body mass index in patients with nonalcoholic fatty liver disease. J Clin Gastroenterol 2013;47(3):280-86.
Grundy SM, Cleeman JI, Daniels SR. Diagnosis and management of the metabolic syndrome: An American Heart Association/National Heart, Lung, and Blood Institute scientific statement. Circulation. 2005; 112:2735–52.
Terrault NA, Bzowej NH, Chang K-M. AASLD guidelines for treatment of chronic hepatitis B. Hepatology 2016;63(1):263-83.
Newsome PN, Cramb R, Davison SM. Guidelines on the management of abnormal liver blood tests. Gut 2018;67(1):6-19.
Prati D, Taioli E, Zanella A. Updated definitions of healthy ranges for serum alanine aminotransferase levels. Ann Intern Med 2002;137(1):1
Kunde SS, Lazenby AJ, Clements RH. Spectrum of NAFLD and diagnostic implications of the proposed new normal range for serum ALT in obese women. Hepatology 2005;42(3):650-56.
Jaycox SH. A fatty world: exploring racial disparity in NAFLD/NASH. Journal of Hepatitis 2016;2(2):1-6
Kruger F, Daniels C, Kidd M, Non-alcoholic fatty liver disease (NAFLD) in the Western Cape: A descriptive analysis S Afr Med J 2010; 100: 168-171.
De Lédinghen,Wong L, Vergniol J Controlled attenuation parameter for the diagnosis of steatosis in non-alcoholic fatty liver disease ,Journal of Gastroenterology and Hepatology 2016 ;(31) : 848–855
Onyekwere AC, Ogbera AO, Balogun BO. Nonalcoholic fatty liver disease and the metabolic syndrome in an urban hospital serving an African community. Ann Hepatol 2011; 10(2):119-24.
Jung L, Hyun W, Kwan S, Value of controlled attenuation parameter in fibrosis prediction in nonalcoholic steatohepatitis, World J Gastroenterol 2019 September 7; 25(33): 4959-4969
Rout G, Saurath K, Nayak B, Controlled attenuation parameter for non-invasive assessment of hepatic steatosis in indian patients ; J clin Exp Hepatol 2018 ; 1-9
Shen F, Zheng R, Yu-Qiang M, Controlled attenuation parameter for non-invasive assessment of hepatic steatosis in Chinese patients, World J Gastroenterol 2014 April 28; 20(16): 4702-4711
Schwenger N,Springer F, Schraml C et al. Non invasive assessment and quantification of liver steatosis by ultrasound,computer tomography and magnetic resonance. J hepatol. 2009 ; ( : 433-45)-131
Carvalhana S, Jorge L, Ana C.How good is controlled attenuation parameter and fatty liver index for assessing liver steatosis in general population: correlation with ultrasound Liver International (2013) John Wiley & Sons A/S.
Sandrin L,Fourquet B, Hasphenoph . Transient elastography : a new non-invasive method for assessment of hepatic fibrosis.Ultrasound Med Biol,29 (2003) ,1705_1713
Friedrich-rust M, Ong MF, Martens S, Performance of transient elastography for the staging of liver fibrosis : a meta-analysis. Gastroenterology,134 (2008) ,960-974
Tsochatzis E , Gurusamy K,Cholongitas, Elastography for the diagnosis of severity of fibrosis in chronic liver disease : a meta analysis of diagnostic accuracy. J Hepatol ,54 (2011) ,650-659
Adams LA, Feldstein AE. Nonalcoholic steatohepatitis : risk factors and diagnosis. Expert Review of Gastroenterology and Hepatology 2010;5:623-35.
Ratziu V, Giral P, Charlotte F. Liver fibrosis in overweight patients. Gastroenterology 2000; 118:1117-23.
Ingh S, Allen AM, Wang Z, et al. Fibrosis progression in nonalcoholic fatty liver vs nonalcoholic steatohepatitis: a systematic review and meta-analysis of paired-biopsy studies. Clin Gastroenterol Hepatol 2015;13:643-54;39-40.
Dulai PS, Singh S, Patel J, et al. Increased risk of mortality by fibrosis stage in nonalcoholic fatty liver disease: Systematic review and meta-analysis. Hepatology 2017;65:15571565.
Downloads
Published
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License CC BY-NC-ND 4.0 that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work