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1.
J Am Heart Assoc ; 13(14): e032192, 2024 Jul 16.
Article in English | MEDLINE | ID: mdl-38979809

ABSTRACT

BACKGROUND: Early age at menarche (AAM) has been associated with a higher risk of carotid artery intima-media thickness (cIMT), an indicator of subclinical vascular disease, albeit the mechanisms underlying this association remain elusive. A better understanding of the relationship between AAM, modifiable cardiometabolic risk factors, and subclinical atherosclerosis may contribute to improved primary prevention and cardiovascular disease treatment. We aimed to investigate the putative causal role of AAM on cIMT, and to identify and quantify the potentially mediatory effects of cardiometabolic risk factors underlying this relationship. METHODS AND RESULTS: We conducted linkage disequilibrium score regression analyses between our exposure of interest, AAM, our outcome of interest, cIMT and potential mediators of the AAM-cIMT association to gauge cross-trait genetic overlap. We considered as mediators the modifiable anthropometric risk factors body mass index (BMI), systolic blood pressure (SBP), lipid traits (total cholesterol, triglycerides, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol), and glycemic traits (fasting glucose). We then leveraged the paradigm of Mendelian randomization to infer causality between AAM and cIMT, and to identify whether cardiometabolic risk factors served as potential mediators of this effect. Our analyses showed that genetically predicted AAM was inversely associated with cIMT, BMI, SBP, and triglycerides, and positively associated with high-density lipoprotein, low-density lipoprotein, and total cholesterol. We showed that the effect of genetically predicted AAM on cIMT may be partially mediated through BMI (20.1% [95% CI, 1.4% to 38.9%]) and SBP (13.5% [95% CI, 0.5%-26.6%]). Our cluster-specific Mendelian randomization revealed heterogeneous causal effect estimates of age at menarche on BMI and SBP. CONCLUSIONS: We highlight supporting evidence for a potential causal association between earlier AAM and cIMT, and almost one third of the effect of AAM on cIMT may be mediated by BMI and SBP. Early intervention aimed at lowering BMI and hypertension may be beneficial in reducing the risk of developing subclinical atherosclerosis due to earlier age at menarche.


Subject(s)
Body Mass Index , Carotid Intima-Media Thickness , Hypertension , Menarche , Mendelian Randomization Analysis , Humans , Female , Menarche/genetics , Hypertension/genetics , Hypertension/epidemiology , Hypertension/physiopathology , Age Factors , Male , Carotid Artery Diseases/genetics , Carotid Artery Diseases/epidemiology , Carotid Artery Diseases/diagnostic imaging , Atherosclerosis/genetics , Atherosclerosis/epidemiology , Sex Factors , Risk Factors , Adolescent , Blood Pressure/genetics , Risk Assessment , Asymptomatic Diseases , Cardiometabolic Risk Factors
2.
Curr Protein Pept Sci ; 21(8): 777-784, 2020.
Article in English | MEDLINE | ID: mdl-31889482

ABSTRACT

Medium-chain fatty acids (MCFAs) are the main form of Medium Chain Triglycerides (MCTs) utilized by monogastric animals. MCFAs can be directly absorbed and supply rapid energy to promote the renewal and repair of intestinal epithelial cells, maintain the integrity of intestinal mucosal barrier function, and reduce inflammation and stress. In our review, we pay more attention to the role of MCFAs on intestinal microbiota and mucosa immunity to explore MCFA's positive effect. It was found that MCFAs and their esterified forms can decrease pathogens while increasing probiotics. In addition, being recognized via specific receptors, MCFAs are capable of alleviating inflammation to a certain extent by regulating inflammation and immune-related pathways. MCFAs may also have a certain value to relieve intestinal allergy and inflammatory bowel disease (IBD). Unknown mechanism of various MCFA characteristics still causes dilemmas in the application, thus MCFAs are used generally in limited dosages and combined with short-chain organic acids (SOAs) to attain ideal results. We hope that further studies will provide guidance for the practical use of MCFAs in animal feed.


Subject(s)
Caprylates/immunology , Colitis, Ulcerative/diet therapy , Crohn Disease/diet therapy , Decanoic Acids/immunology , Irritable Bowel Syndrome/diet therapy , Lauric Acids/immunology , Animal Feed/analysis , Animals , Caprylates/administration & dosage , Caprylates/metabolism , Colitis, Ulcerative/immunology , Colitis, Ulcerative/microbiology , Colitis, Ulcerative/pathology , Crohn Disease/immunology , Crohn Disease/microbiology , Crohn Disease/pathology , Cytokines/genetics , Cytokines/immunology , Decanoic Acids/administration & dosage , Decanoic Acids/metabolism , Gene Expression Regulation/drug effects , Humans , Immunity, Mucosal/drug effects , Intestinal Absorption/drug effects , Intestinal Absorption/immunology , Intestines/drug effects , Intestines/immunology , Intestines/microbiology , Irritable Bowel Syndrome/immunology , Irritable Bowel Syndrome/microbiology , Irritable Bowel Syndrome/pathology , Lauric Acids/administration & dosage , Lauric Acids/metabolism , NF-kappa B/genetics , NF-kappa B/immunology , Stomach/drug effects , Stomach/immunology , Stomach/microbiology , Triglycerides/immunology , Triglycerides/metabolism
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