Non-alcoholic fatty liver disease: a massive problem

Epidemiolotitley

The prevalence of NAFLD assessed by ultrasound is 20–30% in Western adults. NASH is much rarer, affecting 3–16% of healthy living liver donors. NAFLD is strongly associated with the presence and severity of obesity and type 2 diabetes mellitus (T2DM). Studies in severely obese patients (body mass index (BMI) >35 kg/m²) undergoing bariatric surgery have reported prevalences of NAFLD and NASH of 91% and 37%, respectively.¹ The prevalence of NAFLD in T2DM has recently been reported to be 70%.² Even in the absence of obesity and T2DM, NAFLD is closely associated with other features of the metabolic syndrome.

Natural histotitley

Data from retrospective studies have shown that fibrosis progresses in 38% of patients with NAFLD, with necroinflammation on index biopsy the strongest predictor.³ End-stage NASH accounts for 30–75% of all cases of cryptogenic cirrhosis. About 7% of patients with compensated NASH-related cirrhosis will develop hepatocellular carcinoma (HCC) within 10 years, while 50% will require a transplant or die from a liver-related cause.⁴ The overall and liver-related mortality of patients with NAFLD is higher than in age- and sex-matched populations, principally due to increased liver and cardiovascular-related mortality.⁵ Patients with NAFLD have a higher prevalence of micro- and macrovascular disease compared with controls, and increasing evidence supports a direct causal role for NAFLD in the pathogenesis of atheromatous cardiovascular disease.⁶

Clinical presentatititlen

NAFLD is largely asymptomatic, although fatigue is a significant problem.⁷ Most patients are diagnosed after they are found to have unexplained abnormalities of liver blood tests, NAFLD accounting for 60–90% of such cases. History should concentrate on determining the presence of conditions associated with NAFLD and on excluding alternative causes of steatosis, including excessive alcohol intake, previous abdominal surgery and drugs such as amiodarone and tamoxifen.

Investigatiotitles

In the absence of advanced disease, routine liver blood tests are either normal or typically show mild elevations of transaminases, alkaline phosphatase and gamma glutamyl transpeptidase. Ultrasound, computed tomography and routine magnetic resonance imaging are all excellent at detecting steatosis, but none can reliably detect NASH or fibrosis. Newer techniques, including proton magnetic resonance spectroscopy and transient elastography, show promise but require further study prior to routine use for disease staging.

Liver biopsy is not required for diagnostic purposes in a typical patient. However, it may be indicated for accurate disease staging – of importance because different stages of NAFLD have different prognoses and therefore require different management strategies.⁸

Non-invasive markers for staging NAFtitleD

Various clinical and laboratory markers have been shown to be associated with advanced fibrosis (bridging fibrosis or cirrhosis) in NAFLD patients, notably:

• advanced age (>45–50 years)

• BMI > 30kg/m²

• T2DM

• aspartate aminotransferase to alanine aminotransferase (ALT) ratio greater than one.

At present, it would seem reasonable to restrict liver biopsy to patients with at least some of the risk factors. Together with serum markers of inflammation and fibrosis, some risk factors have been combined into a number of different diagnostic algorithms. They all currently require independent validation and comparison before they can be applied to routine clinical practice.⁸ This is also the case for the recently reported diagnostic test for differentiating NASH from simple steatosis.⁹

Overall management stratetitley

Current management strategies are directed at treating, where present, the individual components of the metabolic syndrome. This reduces the risk of cardiovascular disease and may also be beneficial for the liver. This is all that is required for patients with simple steatosis who can be managed by general or primary care physicians in view of the largely benign prognosis. In contrast, patients with more advanced NAFLD require long-term follow-up by hepatologists in light of their increased propensity for disease progression.

Treatments directed at components of the metabolic syndrotitlee

Treatments directed at the livtitler

An increased understanding of the mechanisms of progressive liver damage in NAFLD has stimulated the search for therapies specifically targeting the liver, rather than individual components of the metabolic syndrome that may have beneficial effects. The role of oxidative stress in disease pathogenesis has prompted several studies of antioxidants.¹⁵ Most recently, a large multicentre RCT reported that vitamin E (800 IU/day) improved all histological lesions of NAFLD except fibrosis, and patients on vitamin E had a two-point improvement in NAS score significantly more often than those on placebo.¹² Vitamin E has also been shown to improve NASH features when given in combination with ursodeoxycholic acid (UDCA).¹⁶ The only large, placebo-controlled RCT of UDCA alone in patients with NASH showed no benefit after two years of treatment.

Liver transplantatititlen

Patients with NAFLD who progress to decompensated cirrhosis or develop HCC are candidates for liver transplantation. Perhaps unsurprisingly, steatosis recurs in most patients within four years, with 50% developing NASH and fibrosis. Cases of recurrent cirrhosis are also reported.^17,18 Risk factors for recurrence are:

• the presence of insulin resistance or T2DM pre- and post-transplantation

• weight gain following transplantation

• a high cumulative steroid dose.

These findings highlight the importance of ensuring weight and metabolic control in reducing the risk of disease recurrence in a group of patients who will undoubtedly contribute increasing numbers to transplant programmes in the future.

Key points