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Magnesium Depletion Score and Mortality in Individuals with Metabolic Dysfunction Associated Steatotic Liver Disease over a Median Follow-Up of 26 Years.

Nutrients
January 10, 2025
Lei Fan et al. (8 authors)
Journal ArticleHuman Study
Study Details

Study Goal

The researchers aimed to determine whether the magnesium depletion score (MDS) is associated with all-cause and cardiovascular disease mortality in individuals with MASLD or MetALD.

Results Summary

Higher MDS (>2) was associated with significantly increased all-cause and CVD mortality, particularly in those with inadequate Mg intake or lower fibrosis risk. Correcting Mg deficiency may offer long-term health benefits for high-risk patients.

Population

3802 participants with MASLD or MetALD from the NHANES III cohort.

Effective Dosage

Not specified

Duration

Median follow-up of 26 years

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
higher magnesium depletion score (MDS)
increase
all-cause mortality
participants with MASLD or MetALD
HR, 2.52; 95%CI, 1.77-3.61
was associated with increased
#1
higher magnesium depletion score (MDS)
increase
CVD mortality
participants with MASLD or MetALD
HR, 3.01; 95%CI, 1.87-4.86
was associated with increased
#2
higher magnesium depletion score (MDS)
increase
all-cause mortality
participants who did not meet the estimated average requirement level of Mg intake
HR, 2.72; 95%CI, 1.69-4.37
association became stronger
#3
higher magnesium depletion score (MDS)
increase
all-cause mortality
participants with a Fibrosis-4 index (FIB-4) < 1.3
HR, 2.95; 95%CI, 1.69-5.15
association became stronger
#4
higher MDS, indicative of worse global Mg status
increase
all-cause mortality
individuals with MASLD or MetALD
-
was associated with an increased risk of
#5
higher MDS, indicative of worse global Mg status
increase
CVD mortality
individuals with MASLD or MetALD
-
was associated with an increased risk of
#6
Correcting global Mg deficiency
neutral
-
high-risk MASLD/MetALD patients
-
may have long-term health benefits
#7
Abstract

UNLABELLED: Metabolic dysfunction associated steatotic liver disease (MASLD) has been associated with increased risks of all-cause and cardiovascular disease (CVD) mortality. Identification of modifiable risk factors that may contribute to higher risks of mortality could facilitate targeted and intensive intervention strategies in this population. This study aims to examine whether the magnesium depletion score (MDS) is associated with all-cause and CVD mortality among individuals with MASLD or metabolic and alcohol associated liver disease (MetALD). METHODS: A total of 3802 participants with MASLD or MetALD were followed up over a median of 26 years in the National Health and Nutrition Examination Survey (NHANES) III cohort. The MDS was calculated by aggregating four factors influencing the reabsorption capability of the kidneys. The associations between MDS and all-cause, CVD, and cancer mortality were quantified using Cox proportional hazard regression models. RESULTS: In the combined MASLD + MetALD cohort, a higher MDS (>2) was associated with increased all-cause mortality (HR, 2.52; 95%CI, 1.77-3.61; p-trend < 0.0001) and CVD mortality (HR, 3.01; 1.87-4.86; p-trend < 0.0001) compared to MDS = 0; this association became stronger among participants who did not meet the estimated average requirement level of Mg intake (2.72; 1.69-4.37; p-trend = 0.0014) and those with a Fibrosis-4 index (FIB-4) < 1.3 (2.95; 1.69-5.15; p-trend = 0.0006). CONCLUSIONS: In individuals with MASLD or MetALD, higher MDS, indicative of worse global Mg status, was associated with an increased risk of all-cause and CVD mortality. Correcting global Mg deficiency in high-risk MASLD/MetALD patients may have long-term health benefits.

Medical Subject Headings (MeSH)
HumansMaleFemaleMiddle AgedMagnesiumAdultFollow-Up StudiesCardiovascular DiseasesNutrition SurveysRisk FactorsMagnesium DeficiencyFatty LiverMetabolic DiseasesProportional Hazards Models
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality80/10
Research Impact Scores
APT Score0.05
Weight Score2.60
Normalized Score0.70
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