Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Non-alcoholic fatty liver disease: an emerging driving force in chronic kidney disease

Key Points

  • Accumulating evidence indicates that the presence and severity of non-alcoholic fatty liver disease (NAFLD) is strongly associated with an increased prevalence of chronic kidney disease (CKD)

  • The presence and severity of NAFLD predicts the development of incident CKD, independent of traditional cardiorenal risk factors

  • Evidence suggests that NAFLD exacerbates insulin resistance, predisposes to atherogenic dyslipidaemia, and causes the release of proinflammatory, procoagulant, pro-oxidant and profibrogenic mediators that are important in the pathophysiology of CKD

  • Despite the growing evidence linking NAFLD to CKD, whether a causal association exists has not been definitively established

  • These findings call for a more active and systematic search for NAFLD in patients with CKD with a view to potential earlier treatment

Abstract

Non-alcoholic fatty liver disease (NAFLD) is caused by an accumulation of fat in the liver; the condition can progress over time to increase the risk of developing cirrhosis, end-stage liver disease and hepatocellular carcinoma. The prevalence of NAFLD is increasing rapidly owing to the global epidemics of obesity and type 2 diabetes mellitus (T2DM), and NAFLD has been predicted to become the most important indication for liver transplantation over the next decade. It is now increasingly clear that NAFLD not only affects the liver but can also increase the risk of developing extra-hepatic diseases, including T2DM, cardiovascular disease and chronic kidney disease (CKD), which have a considerable impact on health-care resources. Accumulating evidence indicates that NAFLD exacerbates insulin resistance, predisposes to atherogenic dyslipidaemia and releases a variety of proinflammatory factors, prothrombotic factors and profibrogenic molecules that can promote vascular and renal damage. Furthermore, communication or 'crosstalk' between affected organs or tissues in these diseases has the potential to further harm function and worsen patient outcomes, and increasing amounts of evidence point to a strong association between NAFLD and CKD. Whether a causal relationship between NAFLD and CKD exists remains to be definitively established.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Proposed algorithm for the management of suspected non-alcoholic fatty liver disease (NAFLD) in high-risk individuals.
Figure 2: Organ crosstalk in the pathophysiology of nonalcoholic fatty liver disease (NAFLD) and chronic kidney disease (CKD).
Figure 3: Potential mechanisms by which intestinal dysbiosis might promote the development of non-alcoholic fatty liver disease (NAFLD) and chronic kidney disease (CKD).
Figure 4: Management and therapeutic strategies for non-alcoholic fatty liver disease (NAFLD).

Similar content being viewed by others

References

  1. Chalasani, N. et al. The diagnosis and management of non-alcoholic fatty liver disease: practice guideline by the American Association for the Study of Liver Diseases, American College of Gastroenterology, and the American Gastroenterological Association. Hepatology 55, 2005–2023 (2012).

    Article  PubMed  Google Scholar 

  2. Lonardo, A. et al. Epidemiological modifiers of non-alcoholic fatty liver disease: focus on high-risk groups. Dig. Liver Dis. 47, 997–1006 (2015).

    Article  PubMed  Google Scholar 

  3. European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD) & European Association for the Study of Obesity (EASO). EASL-EASD-EASO clinical practice guidelines for the management of non-alcoholic fatty liver disease. J. Hepatol. 64, 1388–1402 (2016).

  4. Charlton, M. R. et al. Frequency and outcomes of liver transplantation for nonalcoholic steatohepatitis in the United States. Gastroenterology 141, 1249–1253 (2011).

    Article  PubMed  Google Scholar 

  5. Singal, A. K., Hasanin, M., Kaif, M., Wiesner, R. & Kuo, Y. F. Nonalcoholic steatohepatitis is the most rapidly growing indication for simultaneous liver kidney transplantation in the United States. Transplantation 100, 607–612 (2016).

    Article  PubMed  Google Scholar 

  6. Byrne, C. D. & Targher, G. NAFLD: A multisystem disease. J. Hepatol. 62, S47–S64 (2015).

    Article  PubMed  Google Scholar 

  7. Targher, G., Chonchol, M. B. & Byrne, C. D. CKD and nonalcoholic fatty liver disease. Am. J. Kidney Dis. 64, 638–652 (2014).

    Article  PubMed  Google Scholar 

  8. Inker, L. A. et al. KDOQI US commentary on the 2012 KDIGO clinical practice guideline for the evaluation and management of CKD. Am. J. Kidney Dis. 63, 713–735 (2014).

    Article  PubMed  Google Scholar 

  9. McCullough, K. et al. Measuring the population burden of chronic kidney disease: a systematic literature review of the estimated prevalence of impaired kidney function. Nephrol. Dial. Transplant. 27, 1812–1821 (2012).

    Article  PubMed  Google Scholar 

  10. Kendrick, J. & Chonchol, M. B. Nontraditional risk factors for cardiovascular disease in patients with chronic kidney disease. Nat. Clin. Pract. Nephrol. 4, 672–681 (2008).

    Article  PubMed  Google Scholar 

  11. Musso, G. et al. Emerging liver-kidney interactions in nonalcoholic fatty liver disease. Trends Mol. Med. 21, 645–562 (2015).

    Article  CAS  PubMed  Google Scholar 

  12. Hernaez, R. et al. Diagnostic accuracy and reliability of ultrasonography for the detection of fatty liver: a meta-analysis. Hepatology 54, 1082–1090 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  13. Castera, L., Vilgrain, V. & Angulo, P. Noninvasive evaluation of NAFLD. Nat. Rev. Gastroenterol. Hepatol. 10, 666–675 (2013).

    Article  CAS  PubMed  Google Scholar 

  14. Alkhouri, N. & Feldstein, A. E. Noninvasive diagnosis of nonalcoholic fatty liver disease: are we there yet? Metabolism 65, 1087–1095 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Younossi, Z. M. et al. Global epidemiology of nonalcoholic fatty liver disease —meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology 64, 73–84 (2016).

    Article  PubMed  Google Scholar 

  16. Targher, G. et al. Non-alcoholic fatty liver disease is independently associated with an increased prevalence of chronic kidney disease and proliferative/laser-treated retinopathy in type 2 diabetic patients. Diabetologia 51, 444–450 (2008).

    Article  CAS  PubMed  Google Scholar 

  17. Targher, G. et al. Nonalcoholic fatty liver disease is independently associated with an increased prevalence of chronic kidney disease and retinopathy in type 1 diabetic patients. Diabetologia 53, 1341–1348 (2010).

    Article  CAS  PubMed  Google Scholar 

  18. Li, G. et al. Nonalcoholic fatty liver disease associated with impairment of kidney function in nondiabetes population. Biochem. Med. (Zagreb) 22, 92–99 (2012).

    Article  Google Scholar 

  19. Sirota, J. C., McFann, K., Targher, G., Chonchol, M. & Jalal, D. I. Association between nonalcoholic liver disease and chronic kidney disease: an ultrasound analysis from NHANES 1988–1994. Am. J. Nephrol. 36, 466–471 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  20. Ahn, A. L. et al. Non-alcoholic fatty liver disease and chronic kidney disease in Koreans aged 50 years or older. Korean J. Fam. Med. 34, 199–205 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  21. Mikolasevic, I. et al. Chronic kidney disease and nonalcoholic fatty liver disease proven by transient elastography. Kidney Blood Press. Res. 37, 305–310 (2013).

    Article  CAS  PubMed  Google Scholar 

  22. Jia, G. et al. Non-alcoholic fatty liver disease is a risk factor for the development of diabetic nephropathy in patients with type 2 diabetes mellitus. PLoS ONE 10, e0142808 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Pan, L. L. et al. Intrahepatic triglyceride content is independently associated with chronic kidney disease in obese adults: a cross-sectional study. Metabolism 64, 1077–1085 (2015).

    Article  CAS  PubMed  Google Scholar 

  24. Xu, H. W., Hsu, Y. C., Chang, C. H., Wei, K. L. & Lin, C. L. High FIB-4 index as an independent risk factor of prevalent chronic kidney disease in patients with nonalcoholic fatty liver disease. Hepatol. Int. 10, 340–346 (2016).

    Article  PubMed  Google Scholar 

  25. Targher, G. et al. Relationship between kidney function and liver histology in subjects with nonalcoholic steatohepatitis. Clin. J. Am. Soc. Nephrol. 5, 2166–2171 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Yilmaz, Y. et al. Microalbuminuria in nondiabetic patients with nonalcoholic fatty liver disease: association with liver fibrosis. Metabolism 59, 1327–1330 (2010).

    Article  CAS  PubMed  Google Scholar 

  27. Yasui, K. et al. Nonalcoholic steatohepatitis and increased risk of chronic kidney disease. Metabolism 60, 735–739 (2011).

    Article  CAS  PubMed  Google Scholar 

  28. Park, C. W., Tsai, N. T. & Wong, L. L. Implications of worse renal dysfunction and medical comorbidities in patients with NASH undergoing liver transplant evaluation: impact on MELD and more. Clin. Transplant. 25, E606–E611 (2011).

    Article  PubMed  Google Scholar 

  29. Machado, M. V. et al. Impaired renal function in morbid obese patients with nonalcoholic fatty liver disease. Liver Int. 32, 241–248 (2012).

    Article  CAS  PubMed  Google Scholar 

  30. Pacifico, L. et al. The impact of nonalcoholic fatty liver disease on renal function in children with overweight/obesity. Int. J. Mol. Sci. 17, E1218 (2016).

    Article  CAS  PubMed  Google Scholar 

  31. Chang, Y. et al. Nonalcoholic fatty liver disease predicts chronic kidney disease in non-hypertensive and nondiabetic Korean men. Metabolism 57, 569–576 (2008).

    Article  CAS  PubMed  Google Scholar 

  32. Targher, G. et al. Increased risk of CKD among type 2 diabetics with nonalcoholic fatty liver disease. J. Am. Soc. Nephrol. 19, 1564–1570 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Targher, G. et al. Nonalcoholic fatty liver disease is independently associated with an increased incidence of chronic kidney disease in patients with type 1 diabetes. Diabetes Care 37, 1729–1736 (2014).

    Article  CAS  PubMed  Google Scholar 

  34. Musso, G. et al. Association of non-alcoholic fatty liver disease with chronic kidney disease: a systematic review and meta-analysis. PLoS Med. 11, e1001680 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  35. Byrne, C. D., Olufadi, R., Bruce, K. D., Cagampang, F. R. & Ahmed, M. H. Metabolic disturbances in non-alcoholic fatty liver disease. Clin. Sci. (Lond.) 116, 539–564 (2009).

    Article  CAS  Google Scholar 

  36. Scorletti, E., Calder, P. C. & Byrne, C. D. Non-alcoholic fatty liver disease and cardiovascular risk: metabolic aspects and novel treatments. Endocrine 40, 332–343 (2011).

    Article  CAS  PubMed  Google Scholar 

  37. Softic, S., Cohen, D. E. & Kahn, C. R. Role of dietary fructose and hepatic de novo lipogenesis in fatty liver disease. Dig. Dis. Sci. 61, 1282–1293 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Byrne, C. D. Ectopic fat, insulin resistance and non-alcoholic fatty liver disease. Proc. Nutr. Soc. 72, 412–419 (2013).

    Article  CAS  PubMed  Google Scholar 

  39. Lim, S. & Meigs, J. B. Links between ectopic fat and vascular disease in humans. Arterioscler. Thromb. Vasc. Biol. 34, 1820–1826 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Tsaousidou, E. et al. Distinct roles for JNK and IKK activation in Agouti-related peptide neurons in the development of obesity and insulin resistance. Cell Rep. 9, 1495–1506 (2014).

    Article  CAS  PubMed  Google Scholar 

  41. Dong, Y. et al. Activation of the liver X receptor by agonist TO901317 improves hepatic insulin resistance via suppressing reactive oxygen species and JNK pathway. PLoS ONE 10, e0124778 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Perry, R. J., Samuel, V. T., Petersen, K. F. & Shulman, G. I. The role of hepatic lipids in hepatic insulin resistance and type 2 diabetes. Nature 510, 84–91 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Spoto, B., Pisano, A. & Zoccali, C. Insulin resistance in chronic kidney disease: a systematic review. Am. J. Physiol. Renal Physiol. 311, F1087–F1108 (2016).

    Article  CAS  PubMed  Google Scholar 

  44. Willy, J. A., Young, S. K., Stevens, J. L., Masuoka, H. C. & Wek, R. C. CHOP links endoplasmic reticulum stress to NF-kappaB activation in the pathogenesis of nonalcoholic steatohepatitis. Mol. Biol. Cell 26, 2190–2204 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  45. Sharma, M. et al. The riddle of nonalcoholic fatty liver disease: progression from nonalcoholic fatty liver to nonalcoholic steatohepatitis. J. Clin. Exp. Hepatol. 5, 147–158 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  46. Bhatia, L. S., Curzen, N. P., Calder, P. C. & Byrne, C. D. Non-alcoholic fatty liver disease: a new and important cardiovascular risk factor? Eur. Heart J. 33, 1190–1200 (2012).

    Article  CAS  PubMed  Google Scholar 

  47. Targher, G. & Byrne, C. D. Diagnosis and management of nonalcoholic fatty liver disease and its hemostatic/thrombotic and vascular complications. Semin. Thromb. Hemost. 39, 214–228 (2013).

    Article  CAS  PubMed  Google Scholar 

  48. Targher, G., Day, C. P. & Bonora, E. Risk of cardiovascular disease in patients with nonalcoholic fatty liver disease. N. Engl. J. Med. 363, 1341–1350 (2010).

    Article  CAS  PubMed  Google Scholar 

  49. Stefan, N., Kantartzis, K. & Haring, H. U. Causes and metabolic consequences of fatty liver. Endocr. Rev. 29, 939–960 (2008).

    Article  CAS  PubMed  Google Scholar 

  50. Cheng, A. Y. et al. Chronic hepatitis B viral infection independently predicts renal outcome in type 2 diabetic patients. Diabetologia 49, 1777–1784 (2006).

    Article  CAS  PubMed  Google Scholar 

  51. Fabrizi, F., Verdesca, S., Messa, P. & Martin, P. Hepatitis C virus infection increases the risk of developing chronic kidney disease: a systematic review and meta-analysis. Dig. Dis. Sci. 60, 3801–3813 (2015).

    Article  PubMed  Google Scholar 

  52. Zampino, R. et al. Chronic HCV infection and inflammation: clinical impact on hepatic and extra-hepatic manifestations. World J. Hepatol. 5, 528–540 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  53. Adinolfi, L. E. et al. Chronic hepatitis C virus infection and atherosclerosis: clinical impact and mechanisms. World J. Gastroenterol. 20, 3410–3417 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  54. Kamide, K. Role of renin-angiotensin-aldosterone system in metabolic syndrome and obesity-related hypertension. Curr. Hypertens. Rev. 9, 238–245 (2014).

    Article  CAS  Google Scholar 

  55. Cabandugama, P. K., Gardner, M. J. & Sowers, J. R. The renin angiotensin aldosterone system in obesity and hypertension: roles in the cardiorenal metabolic syndrome. Med. Clin. North Am. 101, 129–137 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  56. Goh, G. B. et al. Renin-angiotensin system and fibrosis in non-alcoholic fatty liver disease. Liver Int. 35, 979–985 (2015).

    Article  CAS  PubMed  Google Scholar 

  57. Pelusi, S. et al. Renin-angiotensin system inhibitors, type 2 diabetes and fibrosis progression: an observational study in patients with nonalcoholic fatty liver disease. PLoS ONE 11, e0163069 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Kronenberg, F. Emerging risk factors and markers of chronic kidney disease progression. Nat. Rev. Nephrol. 5, 677–689 (2009).

    Article  CAS  PubMed  Google Scholar 

  59. Massy, Z. A., Stenvinkel, P. & Drueke, T. B. The role of oxidative stress in chronic kidney disease. Semin. Dial. 22, 405–408 (2009).

    Article  PubMed  Google Scholar 

  60. Vlassara, H. et al. Role of oxidants/inflammation in declining renal function in chronic kidney disease and normal aging. Kidney Int. Suppl. 114, S3–S11 (2009).

    Article  CAS  Google Scholar 

  61. Targher, G. et al. Associations between plasma adiponectin concentrations and liver histology in patients with nonalcoholic fatty liver disease. Clin. Endocrinol. (Oxf.) 64, 679–683 (2006).

    Article  CAS  Google Scholar 

  62. Bugianesi, E. et al. Plasma adiponectin in nonalcoholic fatty liver is related to hepatic insulin resistance and hepatic fat content, not to liver disease severity. J. Clin. Endocrinol. Metab. 90, 3498–3504 (2005).

    Article  CAS  PubMed  Google Scholar 

  63. Ix, J. H. & Sharma, K. Mechanisms linking obesity, chronic kidney disease, and fatty liver disease: the roles of fetuin-a, adiponectin, and AMPK. J. Am. Soc. Nephrol. 21, 406–412 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Mehal, W. Z. The gordian knot of dysbiosis, obesity and NAFLD. Nat. Rev. Gastroenterol. Hepatol. 10, 637–644 (2013).

    Article  PubMed  Google Scholar 

  65. Karlsson, F. H. et al. Gut metagenome in European women with normal, impaired and diabetic glucose control. Nature 498, 99–103 (2013).

    Article  CAS  PubMed  Google Scholar 

  66. Qin, J. et al. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature 490, 55–60 (2012).

    Article  CAS  PubMed  Google Scholar 

  67. Larsen, N. et al. Gut microbiota in human adults with type 2 diabetes differs from non-diabetic adults. PLoS ONE 5, e9085 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Utzschneider, K. M., Kratz, M., Damman, C. J. & Hullarg, M. Mechanisms linking the gut microbiome and glucose metabolism. J. Clin. Endocrinol. Metab. 101, 1445–1454 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Wieland, A., Frank, D. N., Harnke, B. & Bambha, K. Systematic review: microbial dysbiosis and nonalcoholic fatty liver disease. Aliment. Pharmacol. Ther. 42, 1051–1063 (2015).

    Article  CAS  PubMed  Google Scholar 

  70. Boursier, J. et al. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology 63, 764–775 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  71. Sampaio-Maia, B., Simoes-Silva, L., Pestana, M., Araujo, R. & Soares-Silva, I. J. The role of the gut microbiome on chronic kidney disease. Adv. Appl. Microbiol. 96, 65–94 (2016).

    Article  CAS  PubMed  Google Scholar 

  72. Nallu, A., Sharma, S., Ramezani, A., Muralidharan, J. & Raj, D. Gut microbiome in chronic kidney disease: challenges and opportunities. Transl Res. 179, 24–37 (2017).

    Article  CAS  PubMed  Google Scholar 

  73. Han, J. L. & Lin, H. L. Intestinal microbiota and type 2 diabetes: from mechanism insights to therapeutic perspective. World J. Gastroenterol. 20, 17737–17745 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. Konturek, P. C. et al. Emerging role of fecal microbiota therapy in the treatment of gastrointestinal and extra-gastrointestinal diseases. J. Physiol. Pharmacol. 66, 483–491 (2015).

    CAS  PubMed  Google Scholar 

  75. Marchesi, J. R. et al. The gut microbiota and host health: a new clinical frontier. Gut 65, 330–339 (2016).

    Article  PubMed  Google Scholar 

  76. Schneeberger, M. et al. Akkermansia muciniphila inversely correlates with the onset of inflammation, altered adipose tissue metabolism and metabolic disorders during obesity in mice. Sci. Rep. 5, 16643 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  77. Simon, M. C. et al. Intake of Lactobacillus reuteri improves incretin and insulin secretion in glucose-tolerant humans: a proof of concept. Diabetes Care 38, 1827–1834 (2015).

    Article  CAS  PubMed  Google Scholar 

  78. Bashiardes, S., Shapiro, H., Rozin, S., Shibolet, O. & Elinav, E. Non-alcoholic fatty liver and the gut microbiota. Mol. Metab. 5, 782–794 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Scorletti, E. & Byrne, C. D. Extrahepatic diseases and nafld: the triangular relationship between nafld, type 2-diabetes and dysbiosis. Dig. Dis. 34 (Suppl. 1), 11–18 (2016).

    Article  PubMed  Google Scholar 

  80. Zhu, L., Baker, R. D. & Baker, S. S. Gut microbiome and nonalcoholic fatty liver diseases. Pediatr. Res. 77, 245–251 (2015).

    Article  CAS  PubMed  Google Scholar 

  81. Psichas, A. et al. The short chain fatty acid propionate stimulates GLP-1 and PYY secretion via free fatty acid receptor 2 in rodents. Int. J. Obes. (Lond.) 39, 424–429 (2015).

    Article  CAS  Google Scholar 

  82. Barcenilla, A. et al. Phylogenetic relationships of butyrate-producing bacteria from the human gut. Appl. Environ. Microbiol. 66, 1654–1661 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Pryde, S. E., Duncan, S. H., Hold, G. L., Stewart, C. S. & Flint, H. J. The microbiology of butyrate formation in the human colon. FEMS Microbiol. Lett. 217, 133–139 (2002).

    Article  CAS  PubMed  Google Scholar 

  84. Hara, E. Relationship between obesity, gut microbiome and hepatocellular carcinoma development. Dig. Dis. 33, 346–350 (2015).

    Article  PubMed  Google Scholar 

  85. Iannelli, F. et al. Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency. Nat. Commun. 5, 3850 (2014).

    Article  CAS  PubMed  Google Scholar 

  86. Neuschwander-Tetri, B. A. et al. Farnesoid X nuclear receptor ligand obeticholic acid for non-cirrhotic, non-alcoholic steatohepatitis (FLINT): a multicentre, randomised, placebo-controlled trial. Lancet 385, 956–965 (2015).

    Article  CAS  PubMed  Google Scholar 

  87. Xu, Y. et al. Farnesoid X receptor activation increases reverse cholesterol transport by modulating bile acid composition and cholesterol absorption in mice. Hepatology 64, 1072–1085 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Wang, Z. et al. Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease. Nature 472, 57–63 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Wang, Z. et al. Non-lethal inhibition of gut microbial trimethylamine production for the treatment of atherosclerosis. Cell 163, 1585–1595 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Tang, W. H. et al. Gut microbiota-dependent trimethylamine N-oxide (TMAO) pathway contributes to both development of renal insufficiency and mortality risk in chronic kidney disease. Circ. Res. 116, 448–455 (2015).

    Article  CAS  PubMed  Google Scholar 

  91. Lassailly, G., Caiazzo, R., Pattou, F. & Mathurin, P. Perspectives on treatment for nonalcoholic steatohepatitis. Gastroenterology 150, 1835–1848 (2016).

    Article  PubMed  Google Scholar 

  92. Corey, K. E. & Rinella, M. E. Medical and surgical treatment options for nonalcoholic steatohepatitis. Dig. Dis. Sci. 61, 1387–1397 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Rotman, Y. & Sanyal, A. J. Current and upcoming pharmacotherapy for non-alcoholic fatty liver disease. Gut 66, 180–190 (2017).

    Article  CAS  PubMed  Google Scholar 

  94. Zhang, H., Zhang, X., Hu, C. & Lu, W. Exenatide reduces urinary transforming growth factor-beta1 and type IV collagen excretion in patients with type 2 diabetes and microalbuminuria. Kidney Blood Press. Res. 35, 483–488 (2012).

    Article  CAS  PubMed  Google Scholar 

  95. Vilar-Gomez, E. et al. Improvement in liver histology due to lifestyle modification is independently associated with improved kidney function in patients with non-alcoholic steatohepatitis. Aliment. Pharmacol. Ther. 45, 332–344 (2017).

    Article  CAS  PubMed  Google Scholar 

  96. Cusi, K. et al. Long-term pioglitazone treatment for patients with nonalcoholic steatohepatitis and prediabetes or type 2 diabetes mellitus: a randomized trial. Ann. Intern. Med. 165, 305–315 (2016).

    Article  PubMed  Google Scholar 

  97. Armstrong, M. J. et al. Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis (LEAN): a multicentre, double-blind, randomised, placebo-controlled phase 2 study. Lancet 385, 956–965 (2015).

    Article  CAS  Google Scholar 

  98. Petit, J. M. et al. Effect of liraglutide therapy on liver fat content in patients with inadequately controlled type 2 diabetes. The Lira-NAFLD study. J. Clin. Endocrinol. Metab. http://dx.doi.org/10.1210/jc.2016-2775 (2016).

  99. Catapano, A. L. et al. 2016 ESC/EAS guidelines for the management of dyslipidaemias: the task force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS) developed with the special contribution of the European Association for Cardiovascular Prevention and Rehabilitation (EACPR). Atherosclerosis 253, 281–344 (2016).

    Article  CAS  PubMed  Google Scholar 

  100. Athyros, V. G. et al. Safety and efficacy of long-term statin treatment for cardiovascular events in patients with coronary heart disease and abnormal liver tests in the Greek Atorvastatin and Coronary Heart Disease Evaluation (GREACE) Study: a post-hoc analysis. Lancet 376, 1916–1922 (2010).

    Article  CAS  PubMed  Google Scholar 

  101. Tikkanen, M. J. et al. Effect of intensive lipid lowering with atorvastatin on cardiovascular outcomes in coronary heart disease patients with mild-to-moderate baseline elevations in alanine aminotransferase levels. Int. J. Cardiol. 168, 3846–3852 (2013).

    Article  PubMed  Google Scholar 

  102. Dongiovanni, P. et al. Statin use and nonalcoholic steatohepatitis in at risk individuals. J. Hepatol. 63, 705–712 (2015).

    Article  CAS  PubMed  Google Scholar 

  103. Singh, S., Singh, P. P., Singh, A. G., Murad, M. H. & Sanchez, W. Statins are associated with a reduced risk of hepatocellular cancer: a systematic review and meta-analysis. Gastroenterology 144, 323–332 (2013).

    Article  CAS  PubMed  Google Scholar 

  104. Athyros, V. G. et al. The effect of statins versus untreated dyslipidaemia on renal function in patients with coronary heart disease. A subgroup analysis of the Greek atorvastatin and coronary heart disease evaluation (GREACE) study. J. Clin. Pathol. 57, 728–734 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  105. Shepherd, J. et al. Effect of intensive lipid lowering with atorvastatin on renal function in patients with coronary heart disease: the Treating to New Targets (TNT) study. Clin. J. Am. Soc. Nephrol. 2, 1131–1139 (2007).

    Article  CAS  PubMed  Google Scholar 

  106. Palmer, S. C. et al. HMG CoA reductase inhibitors (statins) for people with chronic kidney disease not requiring dialysis. Cochrane Database Syst. Rev. 5, CD007784 (2014).

    Google Scholar 

  107. Tonelli, M. & Wanner, C. Lipid management in chronic kidney disease: synopsis of the Kidney Disease: Improving Global Outcomes 2013 clinical practice guideline. Ann. Intern. Med. 160, 182–189 (2014).

    Article  PubMed  Google Scholar 

  108. Bergeron, N., Phan, B. A., Ding, Y., Fong, A. & Krauss, R. M. Proprotein convertase subtilisin/kexin type 9 inhibition: a new therapeutic mechanism for reducing cardiovascular disease risk. Circulation 132, 1648–1666 (2015).

    Article  CAS  PubMed  Google Scholar 

  109. Yokohama, S. et al. Therapeutic efficacy of an angiotensin II receptor antagonist in patients with nonalcoholic steatohepatitis. Hepatology 40, 1222–1225 (2004).

    Article  CAS  PubMed  Google Scholar 

  110. Georgescu, E. F. & Georgescu, M. Therapeutic options in non-alcoholic steatohepatitis (NASH). Are all agents alike? Results of a preliminary study. J. Gastrointestin. Liver Dis. 16, 39–46 (2007).

    PubMed  Google Scholar 

  111. Georgescu, E. F., Ionescu, R., Niculescu, M., Mogoanta, L. & Vancica, L. Angiotensin-receptor blockers as therapy for mild-to-moderate hypertension-associated non-alcoholic steatohepatitis. World J. Gastroenterol. 15, 942–954 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  112. Orlic, L. et al. Nonalcoholic fatty liver disease and the renin-angiotensin system blockers in the patients with chronic kidney disease. Wien. Klin. Wochenschr. 127, 355–362 (2015).

    Article  CAS  PubMed  Google Scholar 

  113. Sanyal, A. J. et al. Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N. Engl. J. Med. 362, 1675–1685 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Jun, M. et al. Antioxidants for chronic kidney disease. Cochrane Database Syst. Rev. 10, CD008176 (2012).

    PubMed  Google Scholar 

  115. Calder, P. C. n-3 fatty acids, inflammation and immunity: new mechanisms to explain old actions. Proc. Nutr. Soc. 72, 326–336 (2013).

    Article  CAS  PubMed  Google Scholar 

  116. Scorletti, E. & Byrne, C. D. Omega-3 fatty acids, hepatic lipid metabolism, and nonalcoholic fatty liver disease. Annu. Rev. Nutr. 33, 231–248 (2013).

    Article  CAS  PubMed  Google Scholar 

  117. Nobili, V. et al. Omega-3 fatty acids: mechanisms of benefit and therapeutic effects in pediatric and adult NAFLD. Crit. Rev. Clin. Lab. Sci. 53, 106–120 (2016).

    Article  CAS  PubMed  Google Scholar 

  118. Sanyal, A. J., Abdelmalek, M. F., Suzuki, A., Cummings, O. W. & Chojkier, M. No significant effects of ethyl-eicosapentanoic acid on histologic features of nonalcoholic steatohepatitis in a phase 2 trial. Gastroenterology 147, 377–384 (2014).

    Article  CAS  PubMed  Google Scholar 

  119. Pacifico, L. et al. A double-blind, placebo-controlled randomized trial to evaluate the efficacy of docosahexaenoic acid supplementation on hepatic fat and associated cardiovascular risk factors in overweight children with nonalcoholic fatty liver disease. Nutr. Metab. Cardiovasc. Dis. 25, 734–741 (2015).

    Article  CAS  PubMed  Google Scholar 

  120. Scorletti, E. et al. Effects of purified eicosapentaenoic and docosahexaenoic acids in nonalcoholic fatty liver disease: results from the WELCOME study. Hepatology 60, 1211–1221 (2014).

    Article  CAS  PubMed  Google Scholar 

  121. Argo, C. K. et al. Effects of n-3 fish oil on metabolic and histological parameters in NASH: a double-blind, randomized, placebo-controlled trial. J. Hepatol. 62, 190–197 (2015).

    Article  CAS  PubMed  Google Scholar 

  122. Scorletti, E. et al. Treating liver fat and serum triglyceride levels in NAFLD, effects of PNPLA3 and TM6SF2 genotypes: results from the WELCOME trial. J. Hepatol. 63, 1476–1483 (2015).

    Article  CAS  PubMed  Google Scholar 

  123. Singh, S., Khera, R., Allen, A. M., Murad, M. H. & Loomba, R. Comparative effectiveness of pharmacological interventions for nonalcoholic steatohepatitis: a systematic review and network meta-analysis. Hepatology 62, 1417–1432 (2015).

    Article  CAS  PubMed  Google Scholar 

  124. Beilfuss, A. et al. Vitamin D counteracts fibrogenic TGF-beta signalling in human hepatic stellate cells both receptor-dependently and independently. Gut 64, 791–799 (2015).

    Article  CAS  PubMed  Google Scholar 

  125. Barchetta, I. et al. Liver vitamin D receptor, CYP2R1, and CYP27A1 expression: relationship with liver histology and vitamin D3 levels in patients with nonalcoholic steatohepatitis or hepatitis C virus. Hepatology 56, 2180–2187 (2012).

    Article  CAS  PubMed  Google Scholar 

  126. Wang, X. X. et al. Vitamin D receptor agonist doxercalciferol modulates dietary fat-induced renal disease and renal lipid metabolism. Am. J. Physiol. Renal Physiol. 300, F801–F810 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  127. Pawlak, M. et al. The transrepressive activity of peroxisome proliferator-activated receptor alpha is necessary and sufficient to prevent liver fibrosis in mice. Hepatology 60, 1593–1606 (2014).

    Article  CAS  PubMed  Google Scholar 

  128. Ratziu, V. et al. Elafibranor, an agonist of the peroxisome proliferator-activated receptor-alpha and -delta, induces resolution of nonalcoholic steatohepatitis without fibrosis worsening. Gastroenterology 150, 1147–1159 (2016).

    Article  CAS  PubMed  Google Scholar 

  129. Souza-Mello, V. Peroxisome proliferator-activated receptors as targets to treat non-alcoholic fatty liver disease. World J. Hepatol. 7, 1012–1019 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  130. Tebay, L. E. et al. Mechanisms of activation of the transcription factor Nrf2 by redox stressors, nutrient cues, and energy status and the pathways through which it attenuates degenerative disease. Free Radic. Biol. Med. 88, 108–146 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  131. Choi, B. H., Kang, K. S. & Kwak, M. K. Effect of redox modulating NRF2 activators on chronic kidney disease. Molecules 19, 12727–12759 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  132. Deng, Y. et al. Shedding of syndecan-1 from human hepatocytes alters very low density lipoprotein clearance. Hepatology 55, 277–286 (2012).

    Article  CAS  PubMed  Google Scholar 

  133. Wang, Y. et al. Plasma cholesteryl ester transfer protein is predominantly derived from Kupffer cells. Hepatology 62, 1710–1722 (2015).

    Article  CAS  PubMed  Google Scholar 

  134. Adepu, S. et al. Hepatic syndecan-1 changes associate with dyslipidemia after renal transplantation. Am. J. Transplant. 14, 2328–2338 (2014).

    Article  CAS  PubMed  Google Scholar 

  135. Miyamoto, S. & Sharma, K. Adipokines protecting CKD. Nephrol. Dial. Transplant. 28 (Suppl. 4), iv15–iv22 (2013).

    PubMed  PubMed Central  Google Scholar 

  136. Berlanga, A., Guiu-Jurado, E., Porras, J. A. & Auguet, T. Molecular pathways in non-alcoholic fatty liver disease. Clin. Exp. Gastroenterol. 7, 221–239 (2014).

    PubMed  PubMed Central  Google Scholar 

  137. Moschen, A. R., Wieser, V. & Tilg, H. Adiponectin: key player in the adipose tissue-liver crosstalk. Curr. Med. Chem. 19, 5467–5473 (2012).

    Article  CAS  PubMed  Google Scholar 

  138. Xie, L. et al. DKK3 expression in hepatocytes defines susceptibility to liver steatosis and obesity. J. Hepatol. 65, 113–124 (2016).

    Article  CAS  PubMed  Google Scholar 

  139. Brenner, C., Galluzzi, L., Kepp, O. & Kroemer, G. Decoding cell death signals in liver inflammation. J. Hepatol. 59, 583–594 (2013).

    Article  CAS  PubMed  Google Scholar 

  140. Kufareva, I., Salanga, C. L. & Handel, T. M. Chemokine and chemokine receptor structure and interactions: implications for therapeutic strategies. Immunol. Cell Biol. 93, 372–383 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  141. Moreno, J. A. et al. Targeting chemokines in proteinuria-induced renal disease. Expert Opin. Ther. Targets 16, 833–845 (2012).

    Article  CAS  PubMed  Google Scholar 

  142. Baeck, C. et al. Pharmacological inhibition of the chemokine C-C motif chemokine ligand 2 (monocyte chemoattractant protein 1) accelerates liver fibrosis regression by suppressing Ly-6C+ macrophage infiltration in mice. Hepatology 59, 1060–1072 (2014).

    Article  CAS  PubMed  Google Scholar 

  143. Pugliese, G., Iacobini, C., Pesce, C. M. & Menini, S. Galectin-3: an emerging all-out player in metabolic disorders and their complications. Glycobiology 25, 136–150 (2015).

    Article  CAS  PubMed  Google Scholar 

  144. Iacobini, C. et al. Galectin-3 ablation protects mice from diet-induced NASH: a major scavenging role for galectin-3 in liver. J. Hepatol. 54, 975–983 (2011).

    Article  CAS  PubMed  Google Scholar 

  145. Nymark, M. et al. Serum lipopolysaccharide activity is associated with the progression of kidney disease in finnish patients with type 1 diabetes. Diabetes Care 32, 1689–1693 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  146. Wu, I. W. et al. p-Cresyl sulphate and indoxyl sulphate predict progression of chronic kidney disease. Nephrol. Dial. Transplant. 26, 938–947 (2011).

    Article  CAS  PubMed  Google Scholar 

  147. Koppe, L. et al. p-Cresyl sulfate promotes insulin resistance associated with CKD. J. Am. Soc. Nephrol. 24, 88–99 (2013).

    Article  CAS  PubMed  Google Scholar 

  148. Vaziri, N. D., Yuan, J., Nazertehrani, S., Ni, Z. & Liu, S. Chronic kidney disease causes disruption of gastric and small intestinal epithelial tight junction. Am. J. Nephrol. 38, 99–103 (2013).

    Article  CAS  PubMed  Google Scholar 

  149. Wong, J. et al. Expansion of urease- and uricase-containing, indole- and p-cresol-forming and contraction of short-chain fatty acid-producing intestinal microbiota in ESRD. Am. J. Nephrol. 39, 230–237 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  150. Skov, J. et al. Glucagon-like peptide-1 (GLP-1): effect on kidney hemodynamics and renin-angiotensin-aldosterone system in healthy men. J. Clin. Endocrinol. Metab. 98, E664–E671 (2013).

    Article  CAS  PubMed  Google Scholar 

  151. Imamura, S., Hirai, K. & Hirai, A. The glucagon-like peptide-1 receptor agonist, liraglutide, attenuates the progression of overt diabetic nephropathy in type 2 diabetic patients. Tohoku J. Exp. Med. 231, 57–61 2013).

    Article  CAS  PubMed  Google Scholar 

  152. Xu, J. et al. Fibroblast growth factor 21 reverses hepatic steatosis, increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice. Diabetes 58, 250–259 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  153. Xu, P. et al. Fibroblast growth factor 21 attenuates hepatic fibrogenesis through TGF-beta/smad2/3 and NF-kappaB signaling pathways. Toxicol. Appl. Pharmacol. 290, 43–53 (2016).

    Article  CAS  PubMed  Google Scholar 

  154. Zhang, J. & Li, Y. Fibroblast growth factor 21 analogs for treating metabolic disorders. Front. Endocrinol. (Lausanne) 6, 168 (2015).

    Google Scholar 

  155. Vallon, V. et al. SGLT2 inhibitor empagliflozin reduces renal growth and albuminuria in proportion to hyperglycemia and prevents glomerular hyperfiltration in diabetic Akita mice. Am. J. Physiol. Renal Physiol. 306, F194–F204 (2014).

    Article  CAS  PubMed  Google Scholar 

  156. Nakano, S. et al. Remogliflozin etabonate improves fatty liver disease in diet-induced obese male mice. J. Clin. Exp. Hepatol. 5, 190–198 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  157. DeFronzo, R. A., Norton, L. & Abdul-Ghani, M. Renal, metabolic and cardiovascular considerations of SGLT2 inhibition. Nat. Rev. Nephrol. 13, 11–26 (2017).

    Article  CAS  PubMed  Google Scholar 

  158. Wanner, C. et al. Empagliflozin and progression of kidney disease in type 2 diabetes. N. Engl. J. Med. 375, 323–334 (2016).

    Article  CAS  PubMed  Google Scholar 

  159. Trionfini, P., Benigni, A. & Remuzzi, G. MicroRNAs in kidney physiology and disease. Nat. Rev. Nephrol. 11, 23–33 (2015).

    Article  CAS  PubMed  Google Scholar 

  160. Leti, F. et al. High-throughput sequencing reveals altered expression of hepatic microRNAs in nonalcoholic fatty liver disease-related fibrosis. Transl Res. 166, 304–314 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  161. Gerhard, G. S. & DiStefano, J. K. Micro RNAs in the development of non-alcoholic fatty liver disease. World J. Hepatol. 7, 226–234 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  162. Gomez, I. G. et al. Anti-microRNA-21 oligonucleotides prevent Alport nephropathy progression by stimulating metabolic pathways. J. Clin. Invest. 125, 141–156 (2015).

    Article  PubMed  Google Scholar 

  163. Dattaroy, D. et al. Micro-RNA 21 inhibition of SMAD7 enhances fibrogenesis via leptin-mediated NADPH oxidase in experimental and human nonalcoholic steatohepatitis. Am. J. Physiol. Gastrointest. Liver Physiol. 308, G298–G312 (2015).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

G.T. is supported in part by grants from the University School of Medicine of Verona, Verona, Italy. C.D.B. is supported in part by the Southampton National Institute for Health Research Biomedical Research Centre.

Author information

Authors and Affiliations

Authors

Contributions

Both authors researched the data for the article, provided substantial contributions to discussions of its content, wrote the article and undertook review and/or editing of the manuscript before submission.

Corresponding author

Correspondence to Giovanni Targher.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Supplementary information S1 (table)

Putative effects of changes in molecules and/or pathways relevant to the pathogenesis of NAFLD and CKD (PDF 253 kb)

PowerPoint slides

Glossary

Hepatorenal syndrome

A particular and common type of kidney failure that affects patients with cirrhosis or, occasionally, with fulminant liver failure, who have portal hypertension and ascites. This syndrome involves constriction of the blood vessels in the kidneys and dilation of blood vessels in the splanchnic circulation, which supplies the intestines.

Prothrombin time

Prothrombin time, along with its derived measures of prothrombin ratio and international normalized ratio, are assays to evaluate the extrinsic pathway of coagulation. Prothrombin time is the primary assay used to monitor oral anticoagulant therapy.

L cells

L cells are enteric endocrine cells that secrete peptides that are capable of stimulating insulin secretion and modulating satiety.

Cholestasis

A decrease in bile flow owing to impaired secretion by hepatocytes or to obstruction of bile flow through intrahepatic or extrahepatic bile ducts.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Targher, G., Byrne, C. Non-alcoholic fatty liver disease: an emerging driving force in chronic kidney disease. Nat Rev Nephrol 13, 297–310 (2017). https://doi.org/10.1038/nrneph.2017.16

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nrneph.2017.16

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing