To gather objective evidence for the effectiveness of their interventions, should
responsible clinicians rely on the necessity to better characterize patients with
nonalcoholic fatty liver disease as being affected by the benign or progressive form
(simple fatty liver or nonalcoholic steatohepatitis) and by which means? Disease markers,
imaging tools, histology? Just here, the Author discusses the weaknesses and the strengths
of this approach in every-day practice. Insulin resistance (IR) are due to hepatic
lipotoxicity, which is consequence of the increased flux of free fatty acids towards
the liver. Non-alcoholic fatty liver disease (NAFLD) is a primary hepatic disease
that should be treated in its more severe entity, i.e., nonalcoholic steatohepatitis
(NASH) and for this reason it is essential to distinguish this latter form from the
benign one, i.e., simple fatty liver (FL). The gold standard in order to obtain this
diagnosis is represented by liver biopsy. Alternatively, when the invasive procedure
is risky, the likely correct diagnosis is reached by imaging tools/biochemical markers.
NAFLD is present also in non-obese patients. It was that lifestyle of hunting and
gathering that shaped us; constant and daily activity was stamped into our genes,
as was a dependence on fresh foods (the only kinds that were available). Our human
ancestors during the Palaeolithic period had a diet based on roots, nuts, vegetables,
fruit, meat, organ meats (liver, spleen, heart, tongue, kidneys, brains and intestines)
and insects. A diet in less concordance with our evolutionary legacy (agrarian diet
coupled to an increased salt consumption during modern times) has led to high prevalence
of both obesity/type 2 diabetes (T2D) and non-alcoholic fatty liver disease (NAFLD)
among Western ethnic groups. Due to insufficient adaptation, a possible mechanism
might be the potential to alter glucose homeostasis (insulin resistance, IR). To confirm
this hypothesis, afret adjusting for age, baseline BMI and lifestyle factors such
as exercise and sleep duration, Mozaffarian et al found that the foods most associated
with weight gain over a four-year period were French fries, potato chips, sugary drinks,
meats, sweets and refined grains (1). This point raises more questions than answers:
Is obesity the main cause of IR, worsened by ectopic fat storage in liver, or is a
hepatic “primitive” metabolic defect to determine IR? Encompassing NAFLD a broad spectrum
of illnesses ranges from FL to NASH, cryptogenic liver cirrhosis (likely post-NASH)
and finally NAFLD-related hepato cellular carcinoma, histopathology merits have so
far outstripped the clinical-laboratory ones in nosographically characterizing these
entities. To date, histological assessment of liver steatosis, ballooning, lobular
inflammation in H&E staining coupled to fibrosis detection is considered the best
tool for diagnosis of NASH. As immediate observation, being liver fibrosis a dynamic
process constituted by neo-fibrogenesis and collagenolytic activity, as a major mechanism
of fibrosis resolution (2), its frozen evaluation casts some doubts. Secondly, is
FL really benign? Evaluating the disease progression of NAFLD in a prospective study
with paired liver biopsies at 3 years, patients with simple steatosis could still
develop NASH and fibrosis progression. Weight reduction was associated with non-progressive
disease (3). It is noteworthy to stress that hepatic steatosis could be per se pro-fibrogenic
(4, 5). Is liver inflammation a strictu sensu injury to counteract with every effort
or is it a response to the excessive caloric intake? Are programmed cellular death
and mild necrosis really effects to blame or are they the starting points for liver
regeneration? Changing the subject, "pure" alcoholic fatty liver has been widely assumed
to be benign with very low risk of progression to cirrhosis. Nine out of 88 patients
with a histological diagnosis of alcoholic fatty liver and no evidence of fibrosis
or alcoholic hepatitis, followed for a median of 10.5 years, developed cirrhosis and
a further seven patients showed fibrosis. Independent histological predictors of progression
on index biopsy were the presence of mixed macro/micro vesicular fat and of giant
mitochondria. Authors concluded that patients with these features should be counseled
intensively regarding their alcohol consumption (6). We can no longer regard alcoholic
fatty liver as benign, in the presence of continuing high alcohol consumption. Why
do we suppose that it is unlikely (the progression) for patients with nonalcoholic
simple fatty liver who continue to be obese or suffer from T2D, in absence of long-lasting
epidemiological studies? Similarly, what is the basic mechanism that links the metabolic
syndrome-associated co-morbidities, i.e., drug induced liver injury, NAFLD, obstructive
sleep apnea syndrome, polycystic ovarian syndrome and alcoholic liver diseases? Hypoxia
induced by mitochondrial dysfunction. To gather objective evidence for the effectiveness
of their interventions, when dealing with NAFLD patients, should responsible clinicians
rely on the necessity to better characterize them as being affected by the benign
or progressive form and by which means? Despite a low rate of overall complications,
percutaneous liver biopsy remains an invasive procedure with the risk of potentially
lethal hemorrhage and infections and is further complicated in the growing number
of obese patients with NAFLD. “Doctor, do I need to undergo liver biopsy, or don’t
I?” These words could be heard through the walls of any hepatologist’s office quite
often. Liver biopsy should be recommended only when the results would affect the treatment
or the management of hepatic diseases due to the health risks. To overcome this limitation,
clinical, instrumental and laboratory variables (readily/rarely available) help predict
the presence of NASH (each researcher cheering on his/her proposed tool). Being the
hepatocyte the ultimate adipocyte (7), intended as situs of ectopic fat storage, calories
control is mandatory to reduce IR due to the low grade chronic inflammation, hallmark
of obesity (8). Nobody pretends that achieving and maintaining an ideal weight is
an easy thing to do. People struggle to keep weight off because they are surrounded
by food, inundated with food messages and constantly presented with opportunities
to eat. Human beings are the only species in the world that has figured out how to
be in complete control of its own food supply. The challenge now is to make sure the
food does not take control of us. The CDC recommends that all adults get a minimum
of 150 minutes of moderate aerobic activity per week, or 75 minutes a week of a vigorous
activity. Is it always compatible with our life style? What about drugs exclusively
used on NASH patients? Patients on pioglitazone plus low hypo caloric diet (LHD) for
six months showed a greater reduction in necroinflammation than patients in the placebo
plus LHD group, but the reduction in fibrosis did not differ significantly (9). Again,
serum ALT levels were reduced with vitamin E and with pioglitazone (along 96 weeks),
as compared with placebo and both agents were associated with reductions in hepatic
steatosis and lobular inflammation but not with improvement in the more important
fibrosis scores (10). Neither vitamin E nor metformin at 72 and 96 weeks was superior
to placebo in attaining the sustained reduction in ALT level (primary outcome) in
patients aged 8-17 years. Compared with placebo, neither therapy demonstrated significant
improvements on steatosis, inflammation, nor fibrosis as individual components at
histology (secondary outcome, intentionally) (11). A recent meta-analysis showed that
thiazolidinediones significantly improve ballooning degeneration, lobular inflammation,
steatosis and combined necroinflammation, but not the key feature, i.e., fibrosis
(12). All in all, prescribing to take some cups of coffee pro die (13) could turn
out to be a good choice to counteract the risk of NAFLD. Being this the best piece
of advice, should clinicians clutch at straws and suggest patients should undergo
liver biopsy? On the contrary, they ought to focus on diagnosis of potential NAFLD-associated
diseases and adequate evaluation of cardio-vascular risk. In medicine, “gold” standard
test refers to a diagnostic test that is the best available under reasonable conditions.
It does not have to be necessarily the best possible test (in case of NAFLD: autopsy
or a two/three decade-follow-up) for the condition in absolute terms. The astonishing
observation is that some studies have suggested a certain rate of disagreement or
interpretational errors in evaluating the histology features. It is advisable to look
at these figures. In a large cohort, on the basis of canonical criteria, definite
NASH was diagnosed in 58.1%, borderline NASH in 19.5% and "not definite NASH” in 22%.
The NAFLD activity score (NAS) was ≥ 5 in 50% and ≤ 4 in 49%; only 75% of biopsies
with definite NASH had an NAS ≥ 5, whereas 28% of borderline and 7% of "not NASH"
biopsies had NAS ≥ 5. Of biopsies with an NAS ≥ 5, 86% had definite NASH and 3% "not
definite NASH". NAS ≤ 4 did not indicate benign histology; in fact, 29% had definite
NASH and only 42% had "no definite NASH". This study was undertaken using a large
dataset of prospectively obtained clinical data and results from liver biopsies blindly
reviewed by a committee comprised of the pathologists from 9 different centers. The
aim was to evaluate if the diagnosis of NASH made by the pathologists correlated with
a threshold value of feature-based scores that comprise the NAS of ≥ 5. Authors do
not recommend it beyond clinical trials (14). It is, however, increasingly apparent
from ongoing and published studies that the numeric value of the composite NAS is
considered by some investigators to be either “synonymous” with, or actually a replacement
for, a microscopic diagnosis that is based on overall pattern of injury as well as
the presence of additional lesions such as zonality of lesions, portal inflammation,
and fibrosis. In fact, Hjelkrem et al claim that a NAS ≥ 4 has optimal sensitivity
and specificity for predicting NASH, and is the recommended value for admission into
an interventional trial for NASH (15). On the other hand, the diagnoses of NASH by
the original NASH subtypes and by a current study's definition of NASH were in moderate
agreement with NAS (κ = 0.47 and κ = 0.51, respectively) and only in fair to moderate
with the Brunt’s criteria (κ = 0.365 and κ = 0.44, respectively) (16). Again, although
the simple and reproducible NAS was found to be a useful pathologic grading system
in Korean NAFLD patients, however, the proportion of borderline cases based on the
NAS was high. The "wait and see" strategy is necessary for evaluating the long-term
prognosis (17). Clinically important differences exist between community general pathologist
and expert hepatopathologist in assessing NAFLD using the NAS scoring system. More
studies are needed to investigate its suitability for community-based clinical practice
(18). Some hepatologists could object to the attitude towards not differentiating
NASH with and without fibrosis, and could make reasonable claims on the necessity
of detecting fibrosis (presence/entity). Poynard et al state that, even if assessing
liver fibrosis is traditionally performed by liver biopsy, it is an imperfect gold
standard. Thus, non-invasive techniques, liver stiffness measurements and biomarkers
are needed and their wide use is welcome (19). Anyway, there are two schools of thought
and everyone shows grassroots studies in support of his/her own tendency. To lend
credence to their results, some researchers in favor of histology try to couple more
precise methods with the classic ones. In a current investigation on cases of NAFLD,
Mori et al, in order to demonstrate that liver stiffness clearly correlates to fibrosis
(stage F1-F4), performed histopathology but also and mainly morphometric analyses
such as the Sirius red-positive fibrotic area and alpha-SMA-positive area (20). Nevertheless,
there are some pitfalls also in imaging method. It is necessary to highlight that,
even when liver stiffness measurement is feasible, high BMI values, which are a characteristic
of NAFLD patients, negatively affect the diagnostic reliability (21). But, if we consider
that BMI estimates and increased ALT levels (also discovered in simple FL) were independent
factors associated with liver stiffness (22), we should infer that not all the features
of fibrosis are necessarily linked to the NASH presence. On the other hand, it is
surprising that a simple test, with no-adjunctive-cost, such as the FIB4 index (based
on age, AST and ALT levels, and platelet counts) is so rarely adopted/validated, judging
from literature data. In fact, it was superior to other tested noninvasive markers
of fibrosis in Japanese patients with NAFLD, characterized by a high negative predictive
value for excluding advanced fibrosis. Anyway, the Authors pinpoint that the small
number of cases of advanced fibrosis in this cohort means that this study has limited
power for validating the high cut-off point (23). It happens to us all physicians.
We look out into the future, trying our best to make wise decisions, only to find
ourselves staring into the teeth of ferocious and widespread uncertainties. Trying
to find a "robust" strategy, given the increasing prevalence of NAFLD, noninvasive
markers for NASH are proposed as a promising approach for screening reasons in every-day
practice. To test their reliability, these surrogate markers are compared to liver
biopsy as “gold” standard. According to the previously highlighted data on histology
this procedure is far from being both accurate and precise. If our criterion of validity
is not itself really valid are surrogate diagnosis techniques consequently reliable?
Anyway, they represent a trilling discovery like the one (24) that will help us better
figure out the mechanisms of NAFLD (in this case the inflammation). I hope we will
never read the results of a study as the following. Investigating the validity of
parental reports of a history of respiratory disease in their children a survey of
the child’s General Practice records to see whether a diagnosis had been made was
performed. Authors did not conclude that the questionnaire instrument was wrong, but
that the records, the criterion, were inadequate (25). Finally, Aristotle claimed
that the highest level of wisdom was phronesis (prudence). Phronesis is basically
the ability to discern the correct action when there is insufficient scientific evidence
to determine the absolute truth. This is clearly the case for histology (or surrogate
tools/markers) and NASH in every-day practice. Waiting for a better understanding
of mechanisms, clinicians could focus on curing the related co-morbitities of NAFLD
and not on correctly diagnosing NASH.