The proposed protocol is for a systematic review and meta-analysis on the relationship between vitamin A and body mass. The primary objective is to explore the mechanisms between vitamin A and adiposity such as inflammation, dietary intake and body fat. The secondary objective is to look at the extent to which vitamin A is stored in different adipose tissue depots. The protocol outlines the motive and scope for the review, and methodology including the risk of bias, statistical analysis, screening and study criteria.
Background
1 The problem, condition or issueGlobally, an estimated 1.9 billion people are either overweight or obese (WHO et al, 2017). It is well known that obesity is a leading cause for many non-communicable chronic diseases (NCDs) including cardiovascular disease, hypertension, type 2 diabetes (T2D) and cancer. More recently, micronutrient deficiency has been found in obese individuals in Vietnam and Latin American countries such as Mexico and Brazil (Laillou et al, 2014;Garcia et al, 2013;de Souza et al, 2007).Together, these two burdens constitute the double burden of malnutrition. There is increasing evidence indicating an inverse association between micronutrients and individuals with a higher body mass index (BMI), in particular fat soluble vitamins such as vitamin A (Andersen et al, 2006; Suzuki et al, 2006). These studies have also shown that dietary intakes of normal weight, overweight and obese individuals are not drastically different. Moreover, animal studies confirmed that obesity causes vitamin A deficiency, as vitamin A levels and transcriptional signalling is reduced in multiple organs, when serum vitamin A concentrations are in the normal range (Trasino et al, 2015).In humans, low serum vitamin A concentrations have been observed in obese individuals, most likely due to increased uptake into the adipose tissue depot, which is acting as a major body pool for vitamin A (Osth et al, 2014;Bonet et al, 2012;Bonet et al, 2003). Although, there is considerable evidence showing similar observations for other vitamins such as vitamin D, vitamin A plays a key role in the regulation of genes involved in fatty acid oxidation and lipid metabolism (Saneei et al, 2013). Vitamin A has been shown to be associated with a reduced odds of metabolic syndrome (MS), non alcoholic fatty acid liver disease (NAFLD) and dyslipidemia (Beydoun et al, 2012;Botella-Carretero et al, 2010;Albuquerque et al, 2016). Therefore, adequate vitamin A status in key metabolic tissues may lead to favourable reductions in body fat and subsequently reductions in obesity.However, it is not clear if an increase in adiposity is a causal effect of low serum vitamin A concentrations or the result of other physiological and environmental factors (Garcia et al, 2009). For instance, inflammation and dietary intake have been implicated as reasons for reduced serum vitamin A concentrations (Hosseini et al, 2017). Therefore, the proposed review hopes to show the degree at which inflammation and dietary intake each effect seru...