CMHClinical and Molecular HepatologyClin Mol Hepatol2287-27282287-285XThe Korean Association for the Study of the Liver10.3350/cmh.2022.0175cmh-2022-0175SnapshotPersonalized medicine in nonalcoholic fatty liver diseasehttp://orcid.org/0000-0001-8234-4058PirolaCarlos J.12*http://orcid.org/0000-0001-5929-5470SookoianSilvia13*
Institute of Medical Research A Lanari, School of Medicine, University of Buenos Aires, Ciudad Autónoma de Buenos Aires, Argentina
Department of Molecular Genetics and Biology of Complex Diseases, National Scientific and Technical Research Council (CONICET)-University of Buenos Aires, Institute of Medical Research (IDIM), Ciudad Autónoma de Buenos Aires, Argentina
Department of Clinical and Molecular Hepatology, National Scientific and Technical Research Council (CONICET)-University of Buenos Aires, Institute of Medical Research (IDIM), Ciudad Autónoma de Buenos Aires, ArgentinaCorresponding author : Carlos J. Pirola Institute of Medical Research A Lanari, School of Medicine, University of Buenos Aires, Combatientes de Malvinas 3150, Ciudad Autónoma de Buenos Aires 1427, Argentina Tel: +54-11-52873888, Fax: +54-11-52873888, E-mail: pirola.carlos@conicet.gov.arSilvia Sookoian Institute of Medical Research A Lanari, School of Medicine, University of Buenos Aires, Combatientes de Malvinas 3150, Ciudad Autónoma de Buenos Aires 1427, Argentina Tel: +54-11-52873905, Fax: +54-11-52873905, E-mail: ssookoian@intramed.net
SS and CJP should be considered joint senior authors.
Editor: Minjong Lee, Ewha Women’s University College of Medicine, Korea
The keystone of precision medicine in complex traits is to predict the onset and progression of the disease. While there are different paths toward precision medicine [1], genetic assessment may be among the top strategies. The current knowledge of the complete human genome sequence and the availability of next-generation sequencing technologies [2] to decipher individual patients’ genetic make-up also invite fully integrated genomic medicine. Therefore, patients may be classified into high or low risk for disease onset or severity, and therapeutic interventions can be personalized. Most importantly, precision medicine must ensure health benefits across geography, ethnicity, age, and gender.
Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease whose prevalence has reached global epidemic proportions in adults and children [3]. Once diagnosed, the treatment of NAFLD is complex and often requires pharmacological intervention to treat the liver disease and its associated risk factors, such as obesity, arterial hypertension, insulin resistance, and abnormal circulating lipid profiles [4]. Hence, in this complex scenario, NAFLD presents myriad challenges to physicians, researchers, and patients.
With advances in the genetic knowledge of NAFLD and nonalcoholic steatohepatitis (NASH) [1,5,6], it has become possible to use the information for clinical application. For example, genetic data could be leveraged to identify individuals who are at risk of NAFLD or estimate the risk of severe histological outcomes, including NASH-fibrosis, cirrhosis, and hepatocellular carcinoma [5].
The biological information gained through the years should be integrated with clinical data and translated into efficient, cost-effective, and reliable decision-making. This bioinformatics integration increases efficiency in the clinical setting and improves diagnosis, ultimately facilitating disease monitoring and therapeutics while also saving healthcare costs.
Major NAFLD-associated gene variants function in metabolic pathways, including substrate delivery for de novo lipogenesis, mitochondrial energy utilization, lipid droplet assembly, lipolytic catabolism, fatty acid compartmentalization very low density lipoprotein assembly, and secretion pathways [6]. However, variants in some genes, such as rs738409 in PNPLA3 and rs58542926 in TM6SF2, present pleiotropic associations that can even explain some systemic effects on emerging diseases, such as COVID-19 [7]. Pleiotropy analysis in a recent genome-wide association study of unexplained chronic alanine aminotransferase elevation as a proxy for NAFLD revealed that several replicated variants were jointly associated with metabolic and/or inflammatory traits, revealing a complex model of genetic architecture [8].
In addition, genetic knowledge integration, data modeling, and analysis are vital processes at the interface with drug discovery. However, drug discovery and precision medicine require a complete understanding of new technologies and gene and protein biology of the selected target [1].
A unique approach to advancing the identification of genetic factors associated with NAFLD is, for instance, the discovery of disease-specific eQTL (expression quantitative trait loci) [9]. This approach has shown that the rs2291702 variant located in alanine--glyoxylate aminotransferase 2 (AGXT2) gene protects against liver fibrosis in a genotype-dependent manner with the potential for therapeutic interventions [9].
Although the heritability of NAFLD is ~50%, as in other complex diseases, a significant proportion of the disease burden remains unexplained; the so-called “the missing heritability” [1,5]. The concept of the missing heritability includes not only the genetic and epigenetic modifiers [10], but the interaction with environmental exposure and diet [11], as well as highly interconnected and dynamic factors, such as the liver microbiome [12]. Some examples of the poorly explored heritability estimates of NAFLD and NASH that explain the disease variance are rare variants, which probably would have substantial effects on the phenotype, the exploration of structural variation, the assessment of interaction among the involved loci-also known as epistasis, and the genetic diversity of the mitochondrial DNA, among many others [5].
Recently, a human study demonstrated that the variants influencing the risk/protection against NAFLD-histological severity (PNPLA3-rs738409, TM6SF2-rs58542926, MBOAT7-rs641738, and HSD17B13-rs72613567) and a variant influencing macronutrient intake (FGF21-rs838133) may affect the liver microbial DNA composition [13]. The significant variants’ combined effect associated with a polygenic risk score (PRS) suggested a link between the liver metataxonomic profile, host genetics, and cardiovascular risk [13].
The ultimate goal of precision medicine is to estimate the patient’s risk of developing a particular disease. In this regard, PRS is a valuable instrument for stratifying the population risk according to the individual’s genetic profile. However, some challenges remain, including the missing heritability, discovery of rare variants [14,15], and reproducibility of GWAS findings in diverse populations [1]. On the other hand, there is the advantage of potentially distinguishing patients with high or low risk of severe disease [1]. Although outside of the focus of this snapshot, the advances in transcriptomics, proteomics, and metabolomics integrated with genomics in a multi-omics approach [16] are presenting a fascinating scenario for the personalized medicine of NAFLD and comorbidities.
In conclusion, the newly acquired genetic information should be used to improve the understanding of disease pathogenesis, which may allow the early identification of at-risk patients, who would benefit most from early treatment. Potential avenues for future research should focus on the prevention, surveillance, and prognosis assessment of NAFLD and NASH. The ultimate role of precision therapy relies on defining the appropriate prediction strategies for implementing patient-based therapies.
Authors’ contributions
C.J.P Concept of the work, manuscript writing and approval. S.S. Concept of the work, manuscript writing and approval.
Conflicts of Interest
The authors have no conflicts to disclose.
AbbreviationsAGXT2
alanine--glyoxylate aminotransferase 2
eQTL
expression quantitative trait loci
NAFLD
nonalcoholic fatty liver disease
NASH
nonalcoholic steatohepatitis
PRS
polygenic risk score
REFERENCESSookoianSPirolaCJPrecision medicine in nonalcoholic fatty liver disease: new therapeutic insights from genetics and systems biology202026461475SalatinoASookoianSPirolaCJComputational pipeline for next-generation sequencing (NGS) studies in genetics of NASH20222455203222BruntEMWongVWNobiliVDayCPSookoianSMaherJJNonalcoholic fatty liver disease2015115080FriedmanSLNeuschwander-TetriBARinellaMSanyalAJMechanisms of NAFLD development and therapeutic strategies201824908922SookoianSPirolaCJGenetics of nonalcoholic fatty liver disease: from pathogenesis to therapeutics201939124140SookoianSPirolaCJValentiLDavidsonNOGenetic pathways in nonalcoholic fatty liver disease: insights from systems biology202072330346PirolaCJSookoianSPNPLA3 and COVID-19 outcomes: thinking outside the box might explain the biology behind pleiotropic effects of rs738409 on the immune system20214128012804VujkovicMRamdasSLorenzKMGuoXDarlayRCordellHJA multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation202254761771YooTJooSKKimHJKimHYSimHLeeJDisease-specific eQTL screening reveals an anti-fibrotic effect of AGXT2 in non-alcoholic fatty liver disease202175514523PirolaCJSookoianSMetabolic dysfunction-associated fatty liver disease: advances in genetic and epigenetic implications20223395102Vilar-GomezEPirolaCJSookoianSWilsonLABeltPLiangTImpact of the association between PNPLA3 genetic variation and dietary intake on the risk of significant fibrosis in patients with NAFLD20211169941006SookoianSSalatinoACastañoGOLandaMSFijalkowkyCGaraycoecheaMIntrahepatic bacterial metataxonomic signature in non-alcoholic fatty liver disease20206914831491PirolaCJSalatinoAQuintanillaMFCastañoGOGaraycoecheaMSookoianSThe influence of host genetics on liver microbiome composition in patients with NAFLD202276103858BaselliGAJamialahmadiOPelusiSCiociolaEMalvestitiFSaracinoMRare ATG7 genetic variants predispose patients to severe fatty liver disease202277596606PirolaCJFlichmanDDopazoHFernández GianottiTSan MartinoJRohrCA rare nonsense mutation in the glucokinase regulator gene is associated with a rapidly progressive clinical form of nonalcoholic steatohepatitis2018210301036PirolaCJSookoianSMultiomics biomarkers for the prediction of nonalcoholic fatty liver disease severity20182416011615Figure