Burden of NAFLD and the evidence from Africa

The actual prevalence of NAFLD may vary depending on the sensitivity of the detection method used. Whilst liver biopsy remains the gold standard to establish the diagnosis and grade severity, it is limited by its inherent risks and impracticality. Therefore, non-invasive radiologic imaging remains the most useful method of detecting liver steatosis. In a recent meta-analysis of studies using imaging or liver biopsy for diagnosis, the regional prevalence of NAFLD in the world was estimated to be 23.4% in Asia, 23.7% in Europe, 31.8% in the Middle-East, 24.1% in North America, 30.5% in South America and 13.5% in Africa [Reference Younossi, Koenig, Abdelatif, Fazel, Henry and Wymer4]. The reported prevalence of NAFLD from population-based studies in high-income countries (HIC) such as the United States, is 8.1% based on elevated transaminase levels, 18.8% using ultrasound (USS) for diagnosis and 31% with magnetic resonance (MR) spectroscopy [Reference Ioannou, Boyko and Lee5–Reference Browning, Szczepaniak, Dobbins, Nuremberg, Horton, Cohen, Grundy and Hobbs7]. The prevalence in HIC is increasing with the worsening obesity and T2DM epidemics [Reference Neuschwander-Tetri8]. It is interesting to note that the region with the lowest reported prevalence was Africa (13.48%) [Reference Younossi, Stepanova, Negro, Hallaji, Younossi and Lam6]. However, the meta-analysis only included two studies from Africa with a small sample size. Using USS, Almobarak et al. found NAFLD in 20% of 100 asymptomatic Sudanese subjects and Onyekwere et al. reported a prevalence of 4.5% among 44 Nigerians [Reference Almobarak, Barakat, Khalifa, Elhoweris, Elhassan and Ahmed9, Reference Onyekwere, Ogbera and Balogun10] (Table 1). It is indeed questionable whether these data can be extrapolated to all countries in Africa and also highlights the paucity of population-based prevalence data from Africa.

Table 1.

Prevalence of NAFLD in African studies

ALT, alanine transaminase; BMI, body mass index; HDL, high-density lipoprotein; HbA1c, haemoglobin A1c; NAFLD, nonalcoholic fatty liver disease; OW, overweight; Tg, total triglyceride; T2DM, type-2 diabetes; USS, ultrasound; WC, waist circumference.

^a Non-diabetic age and sex matched.

^b Non-diabetic sex-matched only.

^c Male subjects only.

^d Asymptomatic volunteers accompanying a patient.

Insulin resistance has been implicated in the pathogenesis of NAFLD and the current increasing burden of obesity and T2DM which are strongly associated with NAFLD, are believed to be the main drivers of this new scourge worldwide [Reference Younossi, Koenig, Abdelatif, Fazel, Henry and Wymer4, Reference Angulo11, Reference Amiri Dash Atan, Koushki, Motedayen, Dousti, Sayehmiri, Vafaee, Norouzinia and Gholami12]. The prevalence of NAFLD among patients with T2DM is reported to be higher than the general population. A meta-analysis of 17 studies from 11 countries including one from Africa, reported a pooled prevalence of 54% [Reference Amiri Dash Atan, Koushki, Motedayen, Dousti, Sayehmiri, Vafaee, Norouzinia and Gholami12]. There are limited data from Africa, with variable prevalence reported using USS, from 9.5% to 68.8% in Nigeria [Reference Onyekwere, Ogbera and Balogun10, Reference Olusanya, Lesi, Adeyomoye and Fasanmade13, Reference Afolabi, Ibitoye, Ikem, Omisore, Idowu and Soyoye14], 50.3% in Sudan [Reference Almobarak, Barakat, Suliman, Elmadhoun, Mohamed, Abobaker, Noor, Bushara and Ahmed15] and 73% in Ethiopia [Reference Zawdie, Tadesse, Wolide, Nigatu and Bobasa16] (Table 1). Elevated serum alanine aminotransferase, presumed to be due to NAFLD has been described in South African patients with T2DM; however other causes were not excluded [Reference Paruk, Pirie, Motala and Kolawole17]. Due to scanty data from a few African countries it is difficult to determine whether NAFLD prevalence in the general population or even among patients with T2DM in African countries mirror that described in other countries. The limited data suggest the prevalence of NAFLD in the general population is comparatively lower in Africa, but the prevalence in subjects with T2DM is similar to those reported globally.

NAFLD prevalence using USS or liver biopsy is reported to be higher (57.5–74%) in obese individuals [Reference Angulo11]. NAFLD is considered to be a hepatic manifestation of the metabolic syndrome (MS) and in HIC the prevalence ranges from 47% to 71% in MS patients; MS also confers a higher risk of NASH and fibrosis [Reference Marchesini, Brizi, Bianchi, Tomassetti, Bugianesi, Lenzi, Noor, Bushara and Ahmed18, Reference Ryan, Wilson, Slavin, Best, Jenkins and Desmond19]. Visceral adipose tissue and its surrogate marker, waist circumference, have a stronger association with NAFLD than body mass index (BMI) alone and predispose to a greater risk of NASH and fibrosis [Reference Pang, Zhang, Song, Qu, Xu, Liu and Chang20]. The only African study to report on the prevalence of NAFLD among overweight or obese adults is from South Africa but was non-representative as participants were sourced from a hepatology clinic and only 5% were Black; in that study, of 127 patients who had liver biopsy, the prevalence of NAFLD, simple steatosis, NASH and advanced liver fibrosis was 87, 51, 36 and 17%, respectively [Reference Kruger, Daniels and Kidd21].

Evidence for the impact of ethnicity on NAFLD comes from studies which showed that when compared to Hispanics or Whites, African Americans had a lower prevalence of NAFLD, despite having a greater burden of major risk factors for the disease [Reference Browning, Szczepaniak, Dobbins, Nuremberg, Horton, Cohen, Grundy and Hobbs7, Reference Caldwell, Harris, Patrie and Hespenheide22]. This racial disparity remains unexplained, but it has been speculated that the distribution of adiposity (predominantly subcutaneous rather than visceral among African Americans) may explain some of the observed differences [Reference Caldwell, Harris, Patrie and Hespenheide22]. Supportive evidence for this comes from a study of 106 female volunteers from South Africa which showed that African woman had a lower hepatic fat content on liver computed tomography (CT) scan compared to their Asian Indian and Caucasian counterparts, despite having a higher level of total body fat, subcutaneous body fat, BMI and waist circumference; moreover subcutaneous fat was found to be a significant negative determinant of hepatic fat content [Reference Naran, Haagensen and Crowther23]. It has been proposed that subcutaneous fat serves as a storage depot for circulating triglycerides in the post-prandial state, thereby buffering the flux of free-fatty acids to the liver [Reference Frayn24]. Therefore, visceral adipose tissue, which is associated with insulin resistance, may promote hepatic lipogenesis whilst subcutaneous fat stores may possibly be protective [Reference Naran, Haagensen and Crowther23]. Other factors that may potentially explain the diversity in hepatic fat content across ethnic groups may include the degree of insulin resistance, dysglycaemia, socioeconomic factors that may influence dietary behaviour and genetic factors viz. patatin-like phospholipase domain-containing 3 (PNPLA3) gene [Reference Romeo, Kozlitina, Xing, Pertsemlidis, Cox, Pennacchio, Boerwinkle, Cohen and Hobbs25].

Evidence from HIC indicates that human immunodeficiency virus (HIV)-infected patients on antiretroviral therapy (ART) have a high NAFLD prevalence (35%) using USS [Reference Maurice, Patel, Scott, Patel, Thursz and Lemoine26]. The available data for NAFLD among HIV infected patients in Africa are limited to two studies: a retrospective South African study which reported a prevalence of 28% on liver biopsy and a Nigerian cohort with a prevalence of 13.3% using USS [Reference Hoffmann, Hoffmann, Kensler, Van Watt, Omar, Chaisson, Martinson and Variava27, Reference Lesi, Soyebi and Eboh28]. The Africa region has the highest burden of HIV infection world-wide and accounts for over two-thirds of the global total of new HIV infections [Reference Pustil29]. UNAIDS Fast-Track approach to escalate access to ART to accomplish the 90–90–90 treatment target by 2020 may influence the prevalence of NAFLD in Africa [30]. Already, in eastern and southern Africa, ART use has escalated rapidly between 2010 and 2016 with over 10 million people accessing therapy [Reference Pustil29]. The long-term implications of this rapid implementation of ART in low-income countries on NAFLD prevalence merit further investigation.

The healthcare agenda in sub-Saharan Africa has been dominated by poverty, undernutrition and communicable diseases with less attention paid to non-communicable diseases. However, with the epidemiological transition, rising obesity prevalence is reported from a number of African countries contributing to increasing prevalence of T2DM and other cardiometabolic diseases. From the limited evidence to date, it would appear that there is a high prevalence of NAFLD in T2DM in Africa, similar to that found in the West [Reference Olusanya, Lesi, Adeyomoye and Fasanmade13–Reference Zawdie, Tadesse, Wolide, Nigatu and Bobasa16]. Therefore African nations are yet to experience the full force of this new epidemic and its consequences (NASH, cirrhosis and HCC).

Unmet need for NAFLD data from Africa

A number of unmet needs exist with respect to NAFLD in Africa including the lack of epidemiologic data, the difficulty in explaining racial disparities observed and an incomplete understanding of the influence of body fat distribution on NAFLD prevalence. The potential impact of HIV and ART also requires investigation. What is required as a priority from Africa, are well-designed epidemiologic studies that screen for NAFLD in the general population as well as high-risk groups such as patients with T2DM or obesity. Screening for NAFLD at a population-based level using USS is perhaps the ideal method for resource-poor settings because of its relative cost-effectiveness, though it is limited by a lower sensitivity for detecting milder degrees of steatosis [Reference Bohte, van Werven, Bipat and Stoker31]. The use of elevated transaminase levels lacks sensitivity; MR- and CT-based imaging methods have better sensitivity but are costly. In view of the potential economic impact of NAFLD on health-care resources in Africa, it would be vital to determine the prevalence of fibrosis among these patients. In this regard, using transient elastography (TE) to measure liver stiffness as a surrogate marker of fibrosis, would be more acceptable than liver biopsy [Reference Tapper and Loomba32]. USS-based TE probes can now also quantify liver steatosis and together with the advantage of operator independent data collection and ability to detect fibrosis, makes TE an attractive option for large-scale studies. The UK Biobank MR imaging study has shown that quantifying hepatic fat using non-invasive MR scans in a large cohort is feasible and can provide accurate estimates of prospective risks of NAFLD [Reference Wilman, Kelly, Garratt, Matthews, Milanesi, Herlihy, Gyngell, Neubauer, Bell, Banerjee and Thomas33]. Replication of large-scale initiatives such as this in Africa using MR or TE technology may provide a better understand of the epidemiology of NAFLD across this region.