2,679 results match your criteria: "College of Chinese Medicine[Affiliation]"

Identifying and Estimating Frailty Phenotypes by Vocal Biomarkers: Cross-Sectional Study.

J Med Internet Res

November 2024

Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan.

Background: Researchers have developed a variety of indices to assess frailty. Recent research indicates that the human voice reflects frailty status. Frailty phenotypes are seldom discussed in the literature on the aging voice.

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Lung cancer is a major cause of cancer-related mortality, and radiotherapy is often limited by tumor resistance and side effects. This study explores whether epoxymicheliolide (ECL), a compound from feverfew, can enhance radiotherapy efficacy in lung cancer. We tested ECL on A549 and PC-9 lung cancer cell lines to evaluate its effect on x-ray irradiation.

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Aim: Ergostatrien-3β-ol (EK100) is a bioactive compound found in the fruiting bodies and mycelia of Antrodia cinnamomea and has anti-inflammatory and immunomodulatory properties. This study aims to evaluate the potential of EK100 as a treatment for Sjögren's syndrome (SS).

Methods: We employed a spontaneous SS model in non-obese diabetic (NOD)/Ltj mice to assess the therapeutic potential of EK100.

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Association between Semaglutide and Nonarteritic Anterior Ischemic Optic Neuropathy: A Multinational Population-Based Study.

Ophthalmology

November 2024

Department of Family Medicine, Brown University Warren Alpert Medical School, Providence, Rhode Island; Coastal Medical Lifespan, Providence, Rhode Island. Electronic address:

Purpose: To investigate whether semaglutide increases the risk of nonarteritic anterior ischemic optic neuropathy (NAION) in the general population.

Design: This retrospective cohort study used a deidentified global electronic medical records database. The enrollment period was extended from January 2017 to August 2023, with observations concluding in August 2024.

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Article Synopsis
  • Mulberry leaf polysaccharides (MLP) show potential for treating Type 2 Diabetes Mellitus by reducing blood glucose and lipid levels, improving metabolism, and lowering insulin resistance in T2DM rats.
  • The study found that MLP helped restore gut microbiota balance by increasing beneficial bacteria like Prevotella, Ruminococcus, and Lactobacillus, which is crucial for gut health.
  • MLP also influenced bile acid metabolism by altering the expression of related enzymes and receptors, indicating a connection between gut microbiota and metabolic health in managing diabetes.
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Prenatal diagnosis of 22q11.2 distal deletion syndrome in a fetus associated with perinatal growth restriction but no structural abnormalities.

Taiwan J Obstet Gynecol

November 2024

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Medical Laboratory Science and Biotechnology, College of Medical & Health Science, Asia University, Taichung, Taiwan. Electronic address:

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Mosaicism for r(20) or 46,XY,r(20)(p13q13.3)/46,XY at amniocentesis in a pregnancy with a favorable outcome and no prominent perinatal decrease of the r(20) cell line with no genomic imbalance.

Taiwan J Obstet Gynecol

November 2024

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Medical Laboratory Science and Biotechnology, College of Medical & Health Science, Asia University, Taichung, Taiwan. Electronic address:

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Detection of a heterozygous de novo pathogenic variant in the PTPN11 gene (c.1505 C > T, p.S502L) in a fetus associated with cystic hygroma and congenital heart defects.

Taiwan J Obstet Gynecol

November 2024

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Medical Laboratory Science and Biotechnology, College of Medical & Health Science, Asia University, Taichung, Taiwan. Electronic address:

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Rapid confirmation of maternal origin of trisomy 21 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency, abnormal first-trimester maternal serum screening result and positive non-invasive prenatal testing for trisomy 21.

Taiwan J Obstet Gynecol

November 2024

Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan; Department of Medical Laboratory Science and Biotechnology, College of Medical & Health Science, Asia University, Taichung, Taiwan. Electronic address:

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Article Synopsis
  • Prenatal diagnosis of mosaic trisomy 21 was successfully performed on a 41-year-old woman during an amniocentesis, revealing a mix of normal and abnormal cells in the fetus due to a Robertsonian translocation.
  • Despite initial concerns, subsequent tests showed significant normalization in fetal cells, leading to a reassuring outcome.
  • At 38 weeks, the mother delivered a healthy baby with normal development, confirming that even low-level chromosomal abnormalities can result in positive pregnancy outcomes.
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Article Synopsis
  • A 36-year-old woman underwent amniocentesis during her pregnancy due to her age, revealing mosaic trisomy 21 with varying levels of affected cells.
  • Despite the genetic abnormality, she was advised to continue with the pregnancy and delivered a healthy baby at 37 weeks.
  • Follow-up tests showed that the baby exhibited low-level mosaicism for trisomy 21 but was normal in phenotype and development at 2 months old.
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Article Synopsis
  • The study discusses the prenatal diagnosis of Jacobsen syndrome in a 41-year-old pregnant woman, which was linked to specific chromosomal abnormalities detected through advanced genetic testing.
  • The fetus exhibited multiple congenital anomalies including growth restrictions, heart defects, and physical deformities, prompting amniocentesis for further analysis.
  • Chromosome microarray analysis (CMA) revealed significant deletions and duplications in chromosomes 11 and 8, respectively, confirming the diagnosis and illustrating the effectiveness of CMA in identifying complex genetic issues in prenatal cases.
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Article Synopsis
  • - A 30-year-old woman underwent prenatal ultrasound at 14 weeks and was found to be carrying a fetus with multiple congenital anomalies, prompting chromosome microarray analysis (CMA) after the pregnancy was terminated.
  • - The analysis revealed a significant deletion on chromosome 5 (5q14.3-q31.1), affecting numerous genes, including NR2F1 and MEF2C, indicating a genetic basis for the fetal conditions observed.
  • - CMA proves to be an effective tool in identifying genetic abnormalities in fetuses with unexplained congenital anomalies, highlighting its value in prenatal genetic testing.
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Objective: We present prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis (CMA) in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11) (p11.2p13)ins(11) (q21p11.

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Article Synopsis
  • A case study discussed the use of expanded non-invasive prenatal testing (NIPT) to detect 1p36 deletion syndrome in a 37-year-old woman undergoing pregnancy via in vitro fertilization.* -
  • The NIPT was positive for a genetic issue at 13 weeks, but tragically, the pregnancy ended with intrauterine fetal death after a follow-up amniocentesis, which confirmed chromosomal abnormalities.* -
  • The findings highlight the efficacy of NIPT for early detection of genetic disorders, specifically familial unbalanced reciprocal translocation, which can aid in prenatal genetic counseling.*
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Article Synopsis
  • * A cohort of 4,606 individuals with schizophrenia was compared to another 4,606 without the disease, revealing that schizophrenia patients had a significantly higher risk of T2DM, especially those not treated with APs.
  • * The research suggests that while schizophrenia increases the risk of T2DM, APs may provide some protective effects; however, other unmeasured factors could also influence T2DM risk, pointing to a need for careful monitoring by healthcare providers.
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Current genome-wide association studies (GWAS) for kidney function lack ancestral diversity, limiting the applicability to broader populations. The East-Asian population is especially under-represented, despite having the highest global burden of end-stage kidney disease. We conducted a meta-analysis of multiple GWASs (n = 244,952) on estimated glomerular filtration rate and a replication dataset (n = 27,058) from Taiwan and Japan.

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Article Synopsis
  • Serious AEs are very uncommon, with an occurrence rate of approximately 0.04-0.08 per 10,000 treatments, and may include complications like pneumothorax and nerve injuries, while minor AEs can involve bruising or dizziness.
  • Preventative measures such as careful needle placement, adherence to hygiene standards, and proper technique are crucial for acupuncturists to minimize the risk of AEs.
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Association between Scabies Treatment and Parkinson's Disease: A Nationwide, Population-Based Study.

Pharmaceuticals (Basel)

October 2024

School of Chinese Medicine, Graduate Institute of Integrated Medicine, College of Chinese Medicine, Ph.D. Program for Translational Medicine, College of Medicine, China Medical University, Taichung 404, Taiwan.

Background: Scabies is typically treated with scabicides like lindane, which poses a risk for acute neural toxicity. Lindane's prolonged use, particularly in agriculture, is linked to neurodegenerative diseases, including Parkinson's disease (PD), the second most common neurodegenerative disorder. This study aimed to evaluate whether scabies patients, particularly those treated with topical lindane, are at increased risk of developing PD.

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Article Synopsis
  • Acute kidney injury (AKI) is a serious condition marked by a sudden drop in kidney function, often seen in hospitalized patients, with no specific treatments currently available.
  • This study evaluates the effects of GKA4, its dead probiotic form, and postbiotic GKA4 on AKI induced by cisplatin in mice, using a ten-day oral administration protocol.
  • Results showed that these treatments improved kidney health, reduced harmful proteins linked to cell stress and apoptosis, and enhanced the expression of proteins related to kidney function, highlighting their potential as therapeutic options for AKI.
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Chemogenetic targeting TRPV1 in obesity-induced depression: Unveiling therapeutic potential of eicosapentaenoic acid and acupuncture.

Brain Behav Immun

January 2025

Mind-Body Interface Research Center (MBI-Lab), China Medical University Hospital, Taichung, Taiwan; College of Medicine, China Medical University, Taichung, Taiwan; An-Nan Hospital, China Medical University, Tainan, Taiwan. Electronic address:

The comorbidity of obesity and depression has major public health impacts, highlighting the need to understand their shared mechanisms. This study explored the connection between obesity and depression through the transient receptor potential V1 (TRPV1) signaling pathway, using obese/depressed murine models and clinical data. Mice fed a high-fat diet showed altered TRPV1 pathway expression in brain regions of the mice: downregulated in the medial prefrontal cortex (mPFC) and hippocampus, and upregulated in the hypothalamus and amygdala, influencing depression-like behaviors and inflammation.

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Employing a PhI(OAc)-mediated domino reaction to assemble nitrogen-containing heterocyclic derivatives and assessing their anti-inflammatory activity.

Chem Commun (Camb)

November 2024

College of Chinese Medicine, the First Affiliated Hospital, and Key Laboratory of Xin'an Medicine of the Ministry of Education, Anhui University of Chinese Medicine, Hefei, 230038, P. R. China.

Metal-free radical cascade synthesis of substituted pyrazole derivatives was initiated by PhI(OAc) at 23 °C. This protocol features wide functional group tolerance, a simple purification process without column chromatography, and an oxygen migration. Compound 5 demonstrated significant anti-inflammatory activity, indicating potential for therapy.

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Article Synopsis
  • The study focuses on cognitive frailty (CF), which is when older adults experience both physical weakness and cognitive decline without having Alzheimer's or other dementias, specifically looking at its prevalence in Chinese seniors.
  • After analyzing 56 studies with over 80,000 participants, the prevalence of various CF types ranged from 14.3% in community dwellers to 25.2% in older inpatients, highlighting a significant public health concern.
  • Key factors influencing CF included age, gender, education, nutrition, mental health, physical activity, sleep quality, and existing medical conditions, emphasizing the importance of promoting healthy lifestyle choices to combat CF.
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Background: Hepatocellular carcinoma (HCC) is a highly malignant tumor; however, its immune microenvironment and mechanisms remain elusive. Single-cell sequencing allows for the exploration of immune characteristics within tumor at the cellular level. However, current knowledge regarding the roles of different immune cell populations in liver cancer progression is limited.

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Synthesis and biological evaluation of quinoxaline derivatives as ASK1 inhibitors.

J Enzyme Inhib Med Chem

December 2024

Jiangxi Provincial Key Laboratory of TCM Female Reproductive Health and Related Diseases Research and Transformation, Jiangxi University of Chinese Medicine, Nanchang, PR China.

Inhibiting apoptosis signal regulated kinase 1 (ASK1) is an attractive strategy for treating diseases such as non-alcoholic steatohepatitis and multiple sclerosis. Here, we report the discovery of a dibromo substituted quinoxaline fragment containing as an effective small-molecule inhibitor of ASK1, with an IC value of 30.17 nM.

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