Background: It is known that cardiometabolic diseases are related to Alzheimer´s Disease.
Method: We included 23 residents of Jalisco with at least one first-degree relative with ADAD (ADADG). We rated the participants using the Clinical Dementia Rating (CDR) as CDR = 0 (n = 20, 87%), CDR = 0.5 (n = 2, 9%), and CDR = 2 (n = 1, 4%). Eleven participants were mutation carriers (APP = 9, PSEN1 = 2). We compared the participant's laboratory test results of the fasting plasma glucose (FPG), lipid profile, glycated hemoglobin (HbA1c), and thyroid function test (TFT) to those of 102 Jalisco residents within the same age range (CG).
Result: Three (13%) carrier participants (APP = 3) reported being previously diagnosed with cardiometabolic disease (hypertension = 1, prediabetes = 1, dyslipidemia = 2). For the ADADG, the most common abnormality in the laboratory tests was dyslipidemia (n = 20, 87%; mixed dyslipidemia = 15, 66%). Other abnormalities found on laboratory tests were FPG≥126 mg/dL (n = 3, 13%), HbA1c≥6.5% (n = 7, 30%), and TFT findings compatible with hypothyroidism (n = 1, 4%). Similarly, in the CG, dyslipidemia was also the most prevalent abnormality (n = 15/22, 68%), followed by HbA1c≥6.5% (n = 6/12, 50%), and at last FPG≥126 mg/dL (n = 6/47, 13%). When comparing the ADADG to the CG, we found that the ADADG has a higher frequency of mixed dyslipidemia (χ2 = 5.02, p = .038), lower levels of free thyroxine (1.12±0.16 VS 1.28±0.19; t(37) = 2.8, p = .008), higher levels of triglycerides (187.1±75 VS 147.8±69.8; t(61) = 0.32, p = .04), and higher levels of very low-density apolipoprotein (37.4±15 VS 28.2±11; t(43) = -2.3, p = .024). We did not find any difference in any measure or prevalence when comparing the mutation carrier group, the non-carrier group, and CG.
Conclusion: Dyslipidemia is the most common cardiometabolic abnormality in both ADADG and CG. The frequency of cardiometabolic abnormalities is not related to the presence of any of the two studied mutations. A follow-up study could show if the cardiometabolic abnormalities are related to an earlier onset of ADAD.
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http://dx.doi.org/10.1002/alz.088266 | DOI Listing |
Fluids Barriers CNS
January 2025
Sanders-Brown Center on Aging, College of Medicine, University of Kentucky, 760 Press Ave, 124 HKRB, Lexington, KY, 40536-0679, USA.
Background: Blood-brain barrier dysfunction is one characteristic of Alzheimer's disease (AD) and is recognized as both a cause and consequence of the pathological cascade leading to cognitive decline. The goal of this study was to assess markers for barrier dysfunction in postmortem tissue samples from research participants who were either cognitively normal individuals (CNI) or diagnosed with AD at the time of autopsy and determine to what extent these markers are associated with AD neuropathologic changes (ADNC) and cognitive impairment.
Methods: We used postmortem brain tissue and plasma samples from 19 participants: 9 CNI and 10 AD dementia patients who had come to autopsy from the University of Kentucky AD Research Center (UK-ADRC) community-based cohort; all cases with dementia had confirmed severe ADNC.
Anal Chem
January 2025
Guangdong Provincial Key Laboratory of Food Quality and Safety, South China Agricultural University, Guangzhou 510642, China.
The rapid, sensitive, and accurate detection of paralytic shellfish toxins (PSTs), such as saxitoxin (STX), is critical for protecting human health due to the frequent occurrence of toxic red tides. In this work, to address the low affinity of traditional mouse monoclonal antibodies (m-mAbs), rabbit monoclonal antibodies (r-mAbs) against STX were produced by a single B-cell sorting culture and a cross-selection strategy. The r-mAbs showed 100-fold improvement in sensitivity (IC = 0.
View Article and Find Full Text PDFMycopathologia
January 2025
Sorbonne Université, Inserm U1135, Centre d'Immunologie et de Maladies Infectieuses (Cimi-Paris), AP-HP, Hôpital Saint-Antoine, Service de Parasitologie-Mycologie, 184 rue Faubourg Saint Antoine, 175012, Paris, France.
We present Enterocytozoon bieneusi infection in four patients with autoimmune diseases undergoing prolonged monoclonal antibody therapies. Two patients suffered from inflammatory bowel disease and received anti-TNF therapies, whereas two other patients suffered from systemic lupus erythematosus with renal involvement and received anti-CD20 or anti-BLyS protein therapies. Three out of four patients consulted for diarrhea with abdominal pain without intestinal inflammation or bleeding at the time of sampling.
View Article and Find Full Text PDFKaohsiung J Med Sci
January 2025
Department of Urology, Tianjin First Central Hospital, Tianjin, China.
miR-155 exhibits variable expression in different tumors and fulfills diverse biological roles. However, specific molecular mechanisms by which miR-155-5p, which is under-expressed in prostate cancer (PCa), operates are yet to be elucidated. The role of the enhancer of zeste 2 (EZH2)/miR-155-5p axis in PCa was determined by using bioinformatics tools and performing luciferase reporter assay, chromatin immunoprecipitation PCR, CCK-8 assays, cell migration and invasion assays, RNA isolation, reverse transcription quantity (RT-qPCR) and Western blot.
View Article and Find Full Text PDFBackground: The immune system is substantially involved in the development and progression of age-related cognitive decline and Alzheimer's disease (AD).
Method: As genetic and environmental factors interactively impact these conditions, we investigated how risk factors such as APOE genotype, age, and sex influence immune activation markers and AD biomarkers in cerebrospinal fluid (CSF) in elderly individuals enrolled in the Mayo Clinic Study of Aging cohort. Among cognitively unimpaired individuals aged over 65 at the baseline visit (N=298), we measured 365 CSF immune activation markers using the proximity extension assay.
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