Nutrition & Metabolism最新文献

Background: Animal studies indicate maternal folic acid intake alters offspring amino acids (AAs) and fatty acid profiles, affecting their long-term health. However, human data on specific folate metabolites remain limited. We explored their dynamic associations with neonatal AAs and acylcarnitines (ACs).

Methods: We conducted a prospective cohort study, involving 4130 singleton pregnant women and their neonates. Maternal total folate and related metabolites in red blood cell (RBC), including 5-methyltetrahydrofolate (5-MTHF), tetrahydrofolate (THF), 5-formyltetrahydrofolate (5-CHO-THF), and unmetabolized folic acid (UMFA), were measured in 6-17 (T1), 20-26 (T2), and 32-36 (T3) gestational weeks. Neonatal metabolites, including 11 AAs and 31 ACs, were routinely tested 72 h postpartum using heel blood samples. Linear regression and pathway analysis were used to evaluate associations between maternal folate metabolites with neonatal metabolic pathways.

Results: 5-MTHF and total folate levels significantly increased from T1 to T2 (p < 0.001), and stabilized from T2 to T3 (p > 0.05). THF and 5-CHO-THF levels showed a continuous upward trend (p < 0.001). Conversely, UMFA declined throughout pregnancy (p < 0.001). Total folate and 5-MTHF showed no significant correlations with neonatal metabolism. THF were associated with multiple neonatal metabolites, and the associations peaked in T1 and declined in T2 and T3. THF in T1 positively correlated with phenylalanine and tyrosine, involved in the phenylalanine and tyrosine metabolism. And it was positively associated with 7 ACs and negatively with 9 ACs, involved in the fatty acids β-oxidation. THF in T2 or T3 positively related to arginine, and negatively with citrulline, glycine, and ornithine, involved in the urea cycle and arginine and proline metabolism. 5-CHO-THF displayed similar and weaker impacts, correlated with fatty acids β-oxidation only in T1. UMFA exhibited different and weaker influence, related to the urea cycle, arginine and proline metabolism only in T1.

Conclusions: Although maternal total folate and 5-MTHF levels showed no significant association with neonatal metabolites, maternal certain folate metabolites, especially THF, exhibited trimester-specific associations with neonatal metabolic pathways, warranting clinical attention.

Objective: Sancai Lianmei granules (SCLMG) have demonstrated efficacy in improving glucolipid metabolism disorder, insulin resistance, and oxidative stress markers in both diabetic patients and rodent models. However, there is limited data available regarding the effect of SCLMG on human Metabolic dysfunction-associated fatty liver disease (MAFLD). This research aims to assess the impact of SCLMG on MAFLD in individuals with diabetes.

Methods and research design: Sixty individuals diagnosed with type 2 diabetes mellitus (T2DM) and MAFLD were randomly allocated to one of two groups: the SCLMG group, which received standard treatment for T2DM along with SCLMG at a dose of 15 g three times daily, or the control group, which received standard treatment without SCLMG. The intervention lasted for 12 weeks. Alterations in liver fat content and liver sclerosis were evaluated using FibroScan. Secondary outcome measures included alterations in liver enzymes, fibrosis markers, advanced glycation end products AGEs, and metabolic parameters.

Results: When incorporated into the standard treatment regimen for MAFLD in diabetic patients, SCLMG exhibited an improvement in reducing hepatic steatosis (P = 0.048) while showing no substantial variations in liver stiffness (P = 0.762). Both the SCLMG and control groups revealed a substantial reduction in FibroScan readings at the end of the treatment period compared to baseline. The two groups exhibited substantial disparities in changes in liver enzymes (alanine aminotransferase (ALT) P = 0.018, aspartate aminotransferase (AST) P = 0.006, gamma-glutamyltranspeptidase (GGT) P < 0.001), skin autofluorescence (SAF) (P = 0.012), and metabolic parameters (P < 0.05). Nevertheless, there was a variation between the groups regarding serum procollagen III peptide (PIIIP) levels (P = 0.026), whereas changes in type Ⅳcollagen (CⅣ) (P = 0.265), hyaluronic acid (HA) (P = 0.199), laminin (LN) (P = 0.144), and high-density lipoprotein cholesterol (HDL-C) (P = 0.315) levels were not statistically significant.

Conclusions: SCLMG is beneficial in regulating glucolipid metabolism and liver function. To a certain extent, SCLMG can improve liver steatosis and shows a tendency towards reducing liver sclerosis. Therefore, SCLMG has a good effect on individuals with T2DM and MAFLD.

Trial registration: ChiCTR2000033099|| http://www.chictr.org.cn/ 20 May 2020. REGISTRATION DETAILS AT: https://www.chictr.org.cn/hvshowprojectEN.html?id=34391&v=1.5.

Background: Insulin resistance (IR) is a well-established risk factor for cardiovascular disease (CVD). The metabolic score for insulin resistance (METS-IR) is a novel surrogate marker for IR, yet the association between its long-term cumulative burden and incident CVD remains unexplored, particularly in the Chinese population.

Methods: This prospective study included 5,264 participants (mean age 58.50 years; 46.6% male) from the China Health and Retirement Longitudinal Study (CHARLS). Cumulative average METS-IR was calculated as the mean of measurements from 2011 (baseline) and 2015 (wave 3). Incident CVD events were ascertained via standardized questionnaires. Multivariable logistic regression and restricted cubic spline models were employed to assess associations.

Results: During a 4-year follow-up, 554 (10.5%) incident CVD cases occurred. After full adjustment, each SD increase in cumulative average METS-IR was associated with a 16.1% higher risk of total CVD (OR = 1.161, 95% CI: 1.050-1.282). A significant dose-response relationship was observed (P for trend = 0.003). Crucially, we found a striking organ-specific disparity: the highest quartile of cumulative METS-IR was strongly associated with a 19.8% increased risk of heart disease (OR = 1.509, 95% CI: 1.118-2.046) but not with stroke (OR = 0.902, 95% CI: 0.440-1.865). Subgroup analyses revealed that this association was particularly pronounced among males, normotensive individuals, and current smokers or drinkers.

Conclusions: Cumulative exposure to insulin resistance, quantified by METS-IR, is an independent predictor of CVD, especially heart disease, in middle-aged and older Chinese adults. Our findings highlight the clinical utility of longitudinal METS-IR assessment for early risk stratification and pinpoint specific high-risk populations for targeted preventive strategies.

Background: Dietary therapy, specifically for weight loss, is currently considered first-line therapy for metabolic-associated steatotic liver disease (MASLD). However, increasing recognition of the role of the gut-liver axis in MASLD highlights potential for microbiota-modulating dietary therapy to improve outcomes. This study aimed to explore dietary variables relevant to gut microbiota in MASLD.

Methods: Twenty-five adults with MASLD and 25 healthy controls were recruited using a retrospective case-control design and characterised using 3-day dietary intake records, clinical markers, and shotgun metagenomic sequencing.

Results: MASLD participants consumed less dietary fibre (p = < 0.01), very long chain omega-3 fatty acids (p = 0.02), nuts and seeds (p = 0.03), whole grains (p < 0.01) and vegetables (p = 0.04). Participants with MASLD had lower abundance of Alistipes senegalensis (r=-0.01, p = 0.04), Coprococcus eutactus (r=-0.07, p = 0.006), Faecalibacterium (r=-0.02, p < 0.001), and higher abundance of Ruminococcus torques (r = 0.04, p = 0.02), and less expression of functional pathways associated with ethanol production, methionine, folate and branched-chain amino acid metabolism. Bacterial species and functional pathways more abundant in MASLD were positively associated with intake of added sugars and saturated fat, and negatively associated with unsaturated fatty acid and dietary fibre intake.

Conclusions: Microbiota characteristics differ between individuals with and without MASLD, and this is influenced by dietary intake. Future translation-focused research investigating dietary interventions and the gut-liver-axis in MASLD are warranted.

Objective: Including dairy products in the diet may help reduce the risk of developing cardiovascular disease (CVD). Nevertheless, how various categories of dairy items influence CVD risk remains insufficiently explored. This study aimed to evaluate the associations between different types of dairy products, their intake frequency, fat content, and the risk of CVD, addressing existing research gaps.

Methods: Dairy intake data-including yogurt, cheese, and milk-were obtained from the Global Dietary Database, covering 185 countries between 1990 and 2018. Corresponding CVD burden metrics-including incidence, prevalence, and disability-adjusted life years (DALYs)-were extracted from the Global Burden of Disease study. These data were used to investigate how dairy intake relates to CVD burden globally. Additionally, individual-level data from 30,341 participants in the National Health and Nutrition Examination Survey (NHANES) were analyzed to evaluate the association between dairy product consumption and CVD risk. Finally, directed acyclic graph and causal mediation models were used to confirm whether inflammatory markers partially mediated the association between dairy consumption and CVD risk.

Results: Globally, individuals who consumed greater amounts of milk tended to have a lower risk of CVD. Individually, milk intake was found to be negatively associated with the risk of CVD, coronary heart disease (CHD), and heart attack (HA). Exploratory mediation analysis indicated that systemic inflammatory markers (SIRI), the monocyte-to-lymphocyte ratio (MLR), and the neutrophil-to-lymphocyte ratio (NLR) partially mediated the relationship between milk intake and CVD risk, contributing - 6.09%, -5.02%, and - 4.13% of the total association, respectively. Further analysis showed that individuals who reported drinking milk daily or at least weekly tended to have a lower risk of developing CVD than those who consumed it less than once per week.

Conclusion: Milk intake may offer protective effects against CVD, CHD, and HA, potentially through the mitigation of inflammation. The frequency of milk intake appears to be a key factor influencing CVD risk. These findings highlight the potential public health benefits of promoting regular milk intake as part of a balanced dietary pattern to help reduce the global burden of CVD.

Background and objective: The composite dietary antioxidant index (CDAI) is a tool to assess an individual's comprehensive dietary antioxidant intake profiles. This study aimed to explore the association between energy-adjusted composite dietary antioxidant index (E-CDAI) and sarcopenic obesity (SO).

Methods: Participants from the NHANES cohort (n = 4388) and the Tongde Hospital of Zhejiang Province cohort (n = 276) were enrolled in the present study. Logistic regression analyses were applied to explore the association between E-CDAI (both continuous and quintiles) and SO. Moreover, the mediating effect of inflammatory/nutritional indicators were evaluated to investigate the association between E-CDAI and SO.

Results: In the NHANES cohort, logistic regression demonstrated a significant inverse correlation between E-CDAI and SO (adjust odd ratio (OR)_continuous =0.89, 95% CI = 0.81, 0.98, P = 0.041; adjust OR_Q5vsQ1 =0.44, 95% CI = 0.29, 1.18, P_trend =0.050) In the Chinese population cohort, an inverse correlation also existed between E-CDAI and SO (adjust OR_continuous =0.72, 95% CI = 0.60, 0.87, P < 0.001; adjust OR_Q5vsQ1 =0.30, 95% CI = 0.13, 0.74, P_trend <0.001). Applying data from the NHANES cohort, the mediation analysis indicated that neutrophil-percentage-to-albumin ratio mediated 12.812% and C-reactive protein mediated 6.485% of the associations between E-CDAI and SO.

Conclusion: A decreased E-CDAI score is associated with the increased risk of SO in adults. The association appeared to be partially mediated through inflammatory/nutritional pathways, suggesting that the E-CDAI may serve as a valuable indicator for identification of individuals at risk for SO.