105 results match your criteria: "Fujita Health University School of Medical Sciences.[Affiliation]"

Objective: Epilepsy treatment with anti-seizure medications (ASMs) is based on careful assessment of the balance between the likelihood of further seizures and the risk of side effects of treatment. However, there is currently no established biomarker to ascertain seizure control status with ASMs. High-frequency oscillations (HFOs), transient bursts of EEG activity with frequencies beyond 80 Hz, are a new and promising noninvasive epilepsy biomarker.

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Background: Donor-specific antibodies (DSAs) targeting human leukocyte antigens (HLAs) substantially reduce the longevity of transplanted organs. Desensitization of DSA-positive renal transplant recipients is achieved through intravenous administration of immunoglobulin (IVIg). However, the presence and detectability of anti-HLA antibodies in IVIg preparations following administration are not fully understood.

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Background: Activated partial thromboplastin time (APTT) is susceptible to reagent composition. This study aimed to investigate a large number of specimens and determine the cause of discrepancies.

Method: This study included 18,994 subjects who underwent coagulation tests at our hospital from May 2020 to December 2020.

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  • The study investigates the link between certain cardiovascular disease-related miRNAs (specifically miR-126, miR-197, and miR-223) and the risk of ischemic stroke in elderly survivors of the Great East Japan Earthquake.* -
  • Conducted with 1,192 participants over 60 years old, researchers followed up on stroke cases until 2016 while measuring miRNA levels through advanced techniques.* -
  • Results showed that higher levels of miR-197 significantly increase stroke risk, suggesting its potential as a predictive biomarker for identifying high-risk individuals.*
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The live attenuated human rotavirus vaccine strain RIX4414 (Rotarix) is used worldwide to prevent severe rotavirus-induced diarrhea in infants. This strain was attenuated through the cell culture passaging of its predecessor, human strain 89-12, which resulted in multiple genomic mutations. However, the specific molecular reasons underlying its attenuation have remained elusive, primarily due to the absence of a suitable reverse genetics system enabling precise genetic manipulations.

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Hand osteoarthritis (HOA), characterized by an earlier onset age and reduced susceptibility to mechanical stress compared with knee and hip osteoarthritis, is considered a suitable disease for identifying predictive biomarkers of osteoarthritis. In particular, DNA methylation variants, expected to contribute to HOA susceptibility, hold potential as osteoarthritis biomarkers. In this study, leukocyte DNA methylation patterns were analyzed in blood samples from patients with HOA, aiming to identify disease-specific biomarkers for osteoarthritis.

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Background: Reduced kidney function is a risk factor of cardiovascular and all-cause mortality. This association was demonstrated for several kidney function markers, but it is unclear whether integrating multiple measured markers may improve mortality risk prediction.

Methods: We conducted an exploratory factor analysis (EFA) of serum creatinine- and cystatin C-based estimated glomerular filtration rate [eGFRcre and eGFRcys; derived by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) and European Kidney Function Consortium (EKFC) equations], blood urea nitrogen (BUN), uric acid and serum albumin among 366 758 participants in the UK Biobank without a history of kidney failure.

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To elucidate the seroprevalence and rate of asymptomatic infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in Japanese children, serological analysis was performed using serum samples collected from March 2020 to February 2023. A total of 1493 serum samples were collected during the first study period (March 2020 to February 2021). None of the serum samples was positive for SARS-CoV-2 antibody.

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  • - The study explored the causal relationship between primary aldosteronism (PA) and cardiovascular diseases such as coronary artery disease (CAD), congestive heart failure (CHF), and stroke, using a cross-ancestry meta-analysis of genetic data.
  • - The researchers identified 7 genetic loci linked to PA risk through an extensive analysis of East Asian and European ancestry samples, finding increased risk estimates for CAD, CHF, and stroke among individuals with PA.
  • - The findings suggest that PA significantly raises the risk of various cardiovascular issues, underlining the importance of early screening and intervention for individuals at risk.
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  • The study explored the relationship between polygenic risk scores (PRS) for blood pressure and mortality due to cardiovascular disease (CVD) and all causes, particularly considering environmental lifestyle factors.
  • It analyzed data from 9,296 participants over a median follow-up of 12.6 years, finding that higher PRS groups had significantly increased risks of CVD mortality compared to medium PRS groups.
  • The findings suggest that combining genetic risk factors with lifestyle information could help identify individuals who might benefit from targeted lifestyle interventions, despite the PRS having limited ability to independently predict outcomes.
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Nutritional researches have successfully used animal models to gain new insights into nutrient action. However, comprehensive descriptions of their molecular mechanisms of action remain elusive as appropriate in vitro evaluation systems are lacking. Organoid models can mimic physiological structures and reproduce in vivo functions, making them increasingly utilized in biomedical research for a better understand physiological and pathological phenomena.

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Introduction: Previous Mendelian randomization (MR) studies for the coffee-kidney association have reported inconsistent relationships in European populations and never examined mediators of this association. We aimed to evaluate this causal relationship using two-sample MR among both East Asian and European ancestries and to explore underlying mechanisms using plasma caffeine levels.

Methods: Among East Asians, the largest genome-wide association study (GWAS) results for coffee intake, plasma caffeine levels, and kidney outcomes were obtained from 152,634; 8940; and 47,070 Japanese adults.

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Thioredoxin-interacting protein (TXNIP) plays an important role in glucose metabolism, and its expression is regulated by DNA methylation (DNAm). Although the association between TXNIP DNAm and type 2 diabetes mellitus has been demonstrated in studies with a cross-sectional design, prospective studies are needed. We therefore examined the association between TXNIP DNAm levels and longitudinal changes in glycemic traits by conducting a longitudinal study involving 169 subjects who underwent two health checkups in 2015 and 2019.

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Objective: While diet plays a key role in chronic kidney disease (CKD) management, the potential for diet to impact CKD prevention in the general population is less clear. Using a priori knowledge, we derived disease-related dietary patterns (DPs) through reduced rank regression (RRR) and investigated associations with kidney function, separately focusing on generally healthy individuals and those with self-reported kidney diseases, hypertension, or diabetes mellitus.

Methods: Eight thousand six hundred eighty-six participants from the population-based Cooperative Health Research in South Tyrol study were split into a group free of kidney disease, hypertension and diabetes (n = 6,133) and a group with any of the 3 conditions (n = 2,553).

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  • The study investigated the long-term relationship between mitochondrial DNA copy number (mtDNA-CN) in leukocytes and the risk of all-cause mortality in a Japanese population over roughly 30 years.
  • It involved 814 participants aged between 38 to 80 years and measured mtDNA-CN using blood samples, categorizing levels into low, middle, and high.
  • Results indicated that low mtDNA-CN levels significantly reduced survival rates, particularly in the middle-aged group, highlighting its potential as a predictor for future mortality risk.
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Aims: The developmental origin of health and disease (DOHaD) theory postulates that poor nutrition during fetal life increases the risk of disease later in life. Excessive fructose intake has been associated with obesity, diabetes, and nonalcoholic fatty liver disease, and maternal fructose intake during pregnancy has been shown to affect offspring health. In this study, we investigated the effects of high maternal fructose intake on the liver stem/progenitor cells of offspring.

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Objective: The association between knee osteoarthritis (OA) and miRNAs has been widely reported. However, the utility of miRNAs as predictors of knee osteoarthritis (KOA) progression in longitudinal studies has not been reported. We aimed to identify circulating miRNAs (c-miRNAs) associated with KOA progression in the general population and to examine their potential use as predictors of KOA progression.

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Purpose: High-frequency oscillation (HFO) in scalp electroencephalography is a promising new noninvasive prognostic epilepsy biomarker, but further data are needed to ascertain the utility of this parameter. The present work investigated the association between epileptic activity and scalp HFO in pediatric patients with various types of epilepsy, using multivariable regression models to correct for possible confounding factors.

Methods: The authors analyzed 97 subjects who were divided into groups with active epilepsy (within 1 year of seizure), seizure-free epilepsy (>1 year without seizure), and nonepilepsy.

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Carotenoids have been reported to exert protective effects against age-related diseases via changes in DNA methylation. Although lower DNA methylation is associated with age-related diseases, only a few studies have investigated the factors influencing DNA methylation. Carotenoids may be a factor linking TXNIP to specific pathophysiological functions.

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Concerns about the negative intergenerational effects of excessive fructose intake are being raised, with evidence suggesting that prenatal fructose intake increases susceptibility to metabolic and cognitive dysfunction later in life. In the present study, we hypothesized that prenatal and postnatal fructose intake acts synergistically to impact on hippocampus of adult offspring. Female Sprague-Dawley rats received distilled water or 20% high-fructose corn syrup (HFCS) solution in addition to standard chow throughout gestation and lactation.

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The increasing prevalence of non-alcoholic fatty liver disease (NAFLD) has become a global health problem. NAFLD has few initial symptoms and may be difficult to detect early, so there is need for a minimally invasive early detection marker. We hypothesized that miR-122 and miR-20a levels combined, as the miR-122/miR-20a ratio might detect NAFLD more sensitively.

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Background: Epigenetic studies have reported relationships between dietary nutrient intake and methylation levels. However, genetic variants that may affect DNA methylation (DNAm) pattern, called methylation quantitative loci (mQTL), are usually overlooked in these analyses. We investigated whether mQTL change the relationship between dietary nutrient intake and leukocyte DNAm levels with an example of estimated fatty acid intake and ATP-binding cassette transporter A1 (ABCA1).

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  • - Maternal consumption of high-fructose corn syrup (HFCS) during pregnancy and lactation increases cortisol-like hormone (corticosterone) levels in rat offspring, but the mechanism behind this effect was not clearly understood.
  • - The study focused on monitoring the activities of specific enzymes involved in hormone metabolism and reviewing epigenetic changes in various tissues of the offspring.
  • - Findings revealed that reduced activity of the enzyme 11β-Hsd2 in the kidneys, influenced by the expression of miR-27a, may explain the elevated hormone levels in the offspring, contributing to research in the developmental origins of health issues.
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