Nutrition, inflammation and liver-spleen axis

Crit Rev Food Sci Nutr. 2018;58(18):3141-3158. doi: 10.1080/10408398.2017.1353479. Epub 2017 Nov 30.

Abstract

Chronic low-grade systemic inflammation represents a mechanism common to many diseases linked to atherosclerosis-related pathways. There is a growing body of evidence indicating that the combination of food quantity and quality along with genetic susceptibility are able to induce the aberrant activation of innate immune signalling, which initially contributes to chronic low-grade inflammation. Liver represents the central player to inflammatory response. Dietary/metabolic factors contribute to the pathogenesis of Non-alcoholic Fatty Liver Disease (NAFLD), the main causes of liver disease in the Western world. Enlargement of the spleen, central organ in regulating the inflammation-related immune response, is commonly seen in patients with of NAFLD, depicting the so called "liver-spleen axis." The aim of this review was to provide an at-a-glance overview of the possible bi-directional mechanisms linking nutrition and inflammation, particularly pinpointing the inflammatory effects stemmed by nutrition on "liver-spleen axis." In particular, the role of unhealthy diet, healthy dietary patterns, such as the Mediterranean diet style, dietary vitamins and micronutrients, such as vitamin D or Magnesium, and Glucagon-Like Peptide-1, a well-known incretin released in response to meal intake, will be discussed. The highly variability of the inflammatory response highlights the role of expert nutritionists in refining methodologies apt to assess nutritional epidemiology and to apply appropriate dietary intervention to counteract diet-induced inflammation mechanisms.

Keywords: Nutritionist; Diet; Inflammation;; Liver-spleen Axis;; Nutrition.

Publication types

  • Review

MeSH terms

  • Diet
  • Diet, Healthy
  • Diet, Mediterranean
  • Food Quality
  • Gastrointestinal Microbiome / physiology
  • Genetic Predisposition to Disease
  • Humans
  • Inflammation / etiology
  • Inflammation / genetics
  • Inflammation / physiopathology*
  • Liver / physiopathology*
  • Micronutrients / administration & dosage
  • Non-alcoholic Fatty Liver Disease / etiology
  • Non-alcoholic Fatty Liver Disease / physiopathology
  • Nutritional Status / immunology
  • Nutritional Status / physiology*
  • Spleen / physiopathology*
  • Splenomegaly / etiology
  • Splenomegaly / physiopathology
  • Vitamin D

Substances

  • Micronutrients
  • Vitamin D