Abstract
The relationship between nonalcoholic fatty liver disease (NAFLD) and chronic kidney disease (CKD) has gained considerable scientific interest in adults over the past few years. However, this association has recently emerged in children. Several published studies have suggested a role for NAFLD as a risk factor for CKD from the earliest age, with a potential influence of the major NAFLD risk polymorphisms, resulting in an increased risk of both cardiovascular and metabolic diseases. In view of the progressive course and increased cardiometabolic risk closely related to NAFLD and CKD, we focused on the link between these diseases in childhood.
Keywords: Nonalcoholic fatty liver disease, Chronic kidney disease, Children, Liver
Core Tip: Nonalcoholic fatty liver disease has been linked to chronic kidney disease in childhood. Due to the intrinsic cardiometabolic burden related to both diseases, we highlighted the importance of knowledge of this relationship in pediatric patients.
TO THE EDITOR
We read with interest the review by Mantovani et al[1] on the challenging association of nonalcoholic fatty liver disease (NAFLD) with chronic kidney disease (CKD)[1]. The authors provided a comprehensive overview on this association, linking two chronic diseases with a serious cardiometabolic burden and potentially leading to end-stage organ injury, by discussing both pathophysiological and therapeutic aspects.
In our opinion, it is important to underline that the relationship between NAFLD and CKD already occurs in childhood. Parallel to the increasing prevalence of childhood obesity, NAFLD has become the most common chronic liver disease in pediatric patients[2-4]. As demonstrated in adults, there is convincing evidence in children indicating NAFLD as a risk factor for CKD later in life[5-9]. Owing to the shared metabolic pathogenesis (including ectopic lipid accumulation and insulin resistance)[10], NAFLD has been found to be closely inter-related with renal dysfunction in childhood[9,11-14]. There is compelling evidence of a significant reduction in estimated glomerular filtration rate (eGFR) in obese children with NAFLD[8,12,14], as well as possible modulation of the main NAFLD genes (including the I148M PNPLA3 variant[5,15-17], the E167K allele of TM6SF2, and HSD17B13)[5,15]. Early impairments in renal function (such as reduced eGFR and/or abnormal albuminuria) have been observed in children with obesity and NAFLD and linked to the severity of liver disease[8,12-14].
We wish to draw readers’ attention to the early subclinical renal involvement in children with obesity and NAFLD. In view of the greater cardiometabolic risk (including type 2 diabetes, cardiovascular disease, and metabolic syndrome)[18-21] of these patients and the potential genetic influence of NAFLD polymorphisms, findings from these studies might have important clinical and prognostic implications at an early age. In our opinion, all children with obesity should undergo abdominal ultrasound to detect fatty liver[22], and careful monitoring with intensive lifestyle-dietary intervention programs. In the future, NAFLD management may also include genetic characterization, which could represent a crucial step to counteract the development of cardiovascular and metabolic disorders already occurring in childhood.
Footnotes
Conflict-of-interest statement: Nothing to declare.
Manuscript source: Unsolicited manuscript
Peer-review started: May 4, 2021
First decision: June 12, 2021
Article in press: August 6, 2021
Specialty type: Gastroenterology and hepatology
Country/Territory of origin: Italy
Peer-review report’s scientific quality classification
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P-Reviewer: Ali H, Du Y S-Editor: Fan JR L-Editor: Kerr C P-Editor: Liu JH
Contributor Information
Anna Di Sessa, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy.
Stefano Guarino, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy.
Rosa Melone, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy.
Rossella Francesca De Simone, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy.
Pierluigi Marzuillo, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy. pierluigi.marzuillo@gmail.com.
Emanuele Miraglia del Giudice, Department of Woman, Child, and General and Specialized Surgery, University of Campania Luigi Vanvitelli, Naples 80138, Italy.
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