Editorial
Copyright ©The Author(s) 2024.
World J Hepatol. Jul 27, 2024; 16(7): 980-989
Published online Jul 27, 2024. doi: 10.4254/wjh.v16.i7.980
Table 1 Liver diseases and related comorbidity, risk factors and pathophysiological mechanisms
Liver diseases
Comorbidity/condition
Risk factors and pathophysiology
NAFLDCKDNAFLD (a liver manifestation of MetS) shares with CKD diverse cardiometabolic risk factors such as: hyperuricemia, dyslipidemia, abdominal-obesity, pro-inflammatory state, hypoadiponectin, and a prothrombotic-hypofibrinolytic event[6]
AT (dysfunction), IRAT dysfunction is an important factor involved in the occurrence of NAFLD and IR[9]
NASH, MetS, CVD, T2DM, CKD, HCCMorbidity and mortality in NASH patients the mostly exacerbated by the occurrence of CVD, T2DM or CKD. HCC can poorly lead to NASH progression in the affected individuals. MetS and CVD are mainly responsible for NAFLD mortality; whilst NAFLD comorbidity with CKD and diabete increases CVD mortality[10]
OsteoporosisNAFLD prevalence can reach 85% in patients with obesity. NAFLD and osteoporosis reported clinically and pathologically associated, mainly in elderly and senile patients[21]
PsoriasisPsoriasis patients experienced a high risk of NAFLD, as well as an increase in the levels of adipokines and hepatokines[23]
MAFLDCKDMAFLD reported significantly associated to CKD prevalence and incidence[7]
SARS-CoV-2 (infection)COVID-19 involved in glucose homeostasis alteration, inflammatory cytokines storm, and oxidative stress increase, which may worsen MAFLD state[18]
ALF/CLDHEALF and CLD may trigger HE (a neurological alteration). Pro-inflammatory cytokines (TNF-α, IL-1β and IL-6) release into brain, following microglial cells activation, characterizes neuroinflammation. That neuroinflammation may impair neurotransmission, which induces the both cognitive- and motor- dysfunction[20]