Clin Mol Hepatol > Volume 28(4); 2022 > Article
Lu, Wu, Kao, and Hung: Non-alcoholic fatty liver disease and the risk of dementia: A meta-analysis of cohort studies
Dear Editor,
We read with great interest the a recent large-scale cohort study by Jeong et al. [1], which suggested that non-alcoholic fatty liver disease (NAFLD) was associated with a higher risk for incident dementia (adjusted hazard ratio, 1.05; 95% confidence interval [CI], 1.02–1.08; P=0.001), and was in agreement with another previous study [2]. However, we found that other studies have reported results that contradict the findings of the above studies [3-5]. Therefore, we performed a metaanalysis of cohort studies to investigate the association between NAFLD and the risk for dementia. Since the prevalence of NAFLD has increased significantly in recent years [6], it is critical to investigate any potential association with dementia.
Two authors independently searched PubMed and Embase records up to August 2022. “Non-alcoholic Fatty Liver Disease” and “Dementia” were searched for MeSH terms and free-text searches without language limitations. We included cohort studies reporting the association between NAFLD and dementia incidence, with data provided as hazard ratios and 95% CIs. The Newcastle-Ottawa scale for cohort studies was used to assess the quality of included studies. Two authors independently performed data extraction and quality assessment. Any conflicts were resolved by discussion or by consulting the third author. Of the 1,136 relevant published studies, 1,130 were excluded because they were not original studies (n=643), did not meet the inclusion criteria (n=311), or were duplicates (n=176). Eventually, six cohort studies, including the Jeong et al. [1] study, and other studies [3-5,7,8] were eligible. A total of 2,345,929 patients, with a mean age of 48.2–73.4 years, were included in the meta-analysis.
The RevMan 5.4 software (The Cochrane Collaboration, London, UK) was used to perform the meta-analysis and the I2 test was used to test heterogeneity. A random-effect model was used for the analysis. The pooled hazard ratio from six cohorts was 1.04 (95% CI, 1.00–1.08; P=0.04, I2=63%) (Fig. 1). Heterogeneity was high with an I2 of 63%. Sensitivity analyses were performed to assess the robustness of the meta-analysis. Each study was sequentially excluded for sensitivity analysis. The analysis showed that a few large studies affected the significance of the results [1,7]. However, a relationship between NAFLD and dementia was generally demonstrable. Further subgroup analyses are required to explore the causes of heterogeneity.
To the best of our knowledge, this was the first meta-analysis for the association between NAFLD and the risk for dementia. This meta-analysis indicated that NAFLD was a significant risk factor for dementia. However, due to the heterogeneity of statistical analyses, the results must be interpreted cautiously. Further prospective studies are needed to establish the relationship between NAFLD and dementia. Influence of other factors, including age, sex, ethnicity, and diagnosis, also requires further investigation.

FOOTNOTES

Authors’ contributions
CHH conceived and designed the research; MYW and LYL contributed to the data acquisition; CHH and YSK analyzed the data and interpreted the results; LYL and CHH drafted, edited, and revised the manuscript; All authors reviewed the manuscript.
Conflicts of Interest
The authors declare no conflicts of interest.

Figure 1.
Forest plot of non-alcoholic fatty liver disease and the risk of dementia. SE, standard error; CI, confidence interval; NAFLD, non-alcoholic fatty liver disease.

cmh-2022-0259f1.jpg

Abbreviations

CI
confidence interval
NAFLD
non-alcoholic fatty liver disease

REFERENCES

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