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Salty taste preference, genetic susceptibility, and risk of metabolic dysfunction-associated steatotic liver disease : insights from three prospective cohorts

Zhang, Shunming LU ; Yan, Yan ; Gu, Yeqing ; Wu, Hongmei ; Zhang, Qing ; Liu, Li ; Borné, Yan LU ; Qi, Lu ; Huang, Tao and Chen, Yu-Ming , et al. (2025) In Food & Function
Abstract


Background and aims: Animal studies have suggested that high salt intake might increase the risk of metabolic dysfunction-associated steatotic liver disease (MASLD), but results from populations are mixed, in part due to inadequate salt intake measurement. Salty taste preference is the primary factor leading to salt choice and can reflect habitual salt intake. However, no study has investigated the association between salty taste preference and MASLD. This study aimed to determine the association between salty taste preference and risk of MASLD, while considering genetic predisposition to MASLD.
Methods: This multicohort study used data from the Tianjin Chronic Low-grade Systemic Inflammation and Health (TCLSIH) cohort (
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Background and aims: Animal studies have suggested that high salt intake might increase the risk of metabolic dysfunction-associated steatotic liver disease (MASLD), but results from populations are mixed, in part due to inadequate salt intake measurement. Salty taste preference is the primary factor leading to salt choice and can reflect habitual salt intake. However, no study has investigated the association between salty taste preference and MASLD. This study aimed to determine the association between salty taste preference and risk of MASLD, while considering genetic predisposition to MASLD.
Methods: This multicohort study used data from the Tianjin Chronic Low-grade Systemic Inflammation and Health (TCLSIH) cohort (
n = 16 869), the Guangzhou Nutrition and Health Study (GNHS) cohort (
n = 1225), and the UK Biobank (
n = 179 668). Salty taste preference was assessed using self-reported questionnaires. Incident MASLD was ascertained using abdominal ultrasound or electronic health records. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox proportional hazards models.
Results: During follow-up, we documented 3358 MASLD cases in the TCLSIH cohort, 670 cases in the GNHS cohort, and 1780 cases in the UK Biobank. The adjusted HRs (95% CIs) of incident MASLD across the three cohorts were 1.17 (1.05, 1.30), 1.49 (1.18, 1.88), and 1.13 (1.01, 1.28), comparing high with low salty taste preference. Such associations were mediated by 29.8%-49.4% for body mass index and 49.4%-64.5% for waist circumference. Individuals with high salty taste preference and genetic risk had the strongest risk elevation for MASLD, though no significant interaction was observed.
Conclusion: Salty taste preference, a proxy for long-term salt intake, was positively associated with risk of MASLD, especially in individuals with high genetic predisposition.

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Contribution to journal
publication status
epub
subject
in
Food & Function
publisher
Royal Society of Chemistry
external identifiers
  • pmid:41355483
ISSN
2042-6496
DOI
10.1039/d5fo04464b
language
English
LU publication?
yes
id
6556ee7b-8ef2-446e-9bfd-e1f015b1ed75
date added to LUP
2025-12-09 11:52:10
date last changed
2025-12-09 12:20:54
@article{6556ee7b-8ef2-446e-9bfd-e1f015b1ed75,
  abstract     = {{<p><br>
 Background and aims: Animal studies have suggested that high salt intake might increase the risk of metabolic dysfunction-associated steatotic liver disease (MASLD), but results from populations are mixed, in part due to inadequate salt intake measurement. Salty taste preference is the primary factor leading to salt choice and can reflect habitual salt intake. However, no study has investigated the association between salty taste preference and MASLD. This study aimed to determine the association between salty taste preference and risk of MASLD, while considering genetic predisposition to MASLD.<br>
 Methods: This multicohort study used data from the Tianjin Chronic Low-grade Systemic Inflammation and Health (TCLSIH) cohort (<br>
 n = 16 869), the Guangzhou Nutrition and Health Study (GNHS) cohort (<br>
 n = 1225), and the UK Biobank (<br>
 n = 179 668). Salty taste preference was assessed using self-reported questionnaires. Incident MASLD was ascertained using abdominal ultrasound or electronic health records. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using Cox proportional hazards models.<br>
 Results: During follow-up, we documented 3358 MASLD cases in the TCLSIH cohort, 670 cases in the GNHS cohort, and 1780 cases in the UK Biobank. The adjusted HRs (95% CIs) of incident MASLD across the three cohorts were 1.17 (1.05, 1.30), 1.49 (1.18, 1.88), and 1.13 (1.01, 1.28), comparing high with low salty taste preference. Such associations were mediated by 29.8%-49.4% for body mass index and 49.4%-64.5% for waist circumference. Individuals with high salty taste preference and genetic risk had the strongest risk elevation for MASLD, though no significant interaction was observed.<br>
 Conclusion: Salty taste preference, a proxy for long-term salt intake, was positively associated with risk of MASLD, especially in individuals with high genetic predisposition.<br>
 </p>}},
  author       = {{Zhang, Shunming and Yan, Yan and Gu, Yeqing and Wu, Hongmei and Zhang, Qing and Liu, Li and Borné, Yan and Qi, Lu and Huang, Tao and Chen, Yu-Ming and Niu, Kaijun and Ma, Le and The China Cohort Consortium}},
  issn         = {{2042-6496}},
  language     = {{eng}},
  month        = {{12}},
  publisher    = {{Royal Society of Chemistry}},
  series       = {{Food & Function}},
  title        = {{Salty taste preference, genetic susceptibility, and risk of metabolic dysfunction-associated steatotic liver disease : insights from three prospective cohorts}},
  url          = {{http://dx.doi.org/10.1039/d5fo04464b}},
  doi          = {{10.1039/d5fo04464b}},
  year         = {{2025}},
}