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BioWorld - Monday, June 8, 2026
Home » Topics » Biomarkers, BioWorld Science

Biomarkers, BioWorld Science
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Close-up of elderly eye
Biomarkers

Genetic variation in METTL23 gene tied to normotensive glaucoma

May 9, 2024
Recent findings discovered a mutation in the METTL23 gene, which encodes methyltransferase-like protein 23, in a pedigree of normal-tension glaucoma (NTG). The aim of researchers from the Institute for Vision Research, The University of Iowa Roy J and Lucille A Carver College of Medicine was to confirm an association of mutations in this gene with NTG.
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Biomarkers

miR-199a-3p and miR-100-5 have protective role in autoimmune hepatitis

May 7, 2024
MicroRNAs (miRNAs) are small noncoding RNAs that play important roles in immune response regulation in autoimmune disease such as autoimmune hepatitis. Researchers investigated whether Δ8-tetrahydrocannabinol (THC), which is present in marijuana, could prevent the development of autoimmune hepatitis in treated mice by altering miRNA expression.
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Silhouette of head and brain with DNA double helixes
Neurology/psychiatric

Two copies of APOE4 cause genetic form of Alzheimer’s

May 6, 2024
By Anette Breindl
Based on its analysis of a large cohort of individuals homozygous for the ε4 variant of apolipoprotein E (APOE4), a multinational team of researchers is arguing that homozygosity for APOE4 should be considered a genetic form of Alzheimer’s disease. However, not everyone agrees that the findings warrant reclassifying APOE from risk factor to causal gene. Currently, APOE4 is classified as the strongest risk factor for developing AD. Another variant, the APOE2 variant, is protective, while APOE3 is neutral.
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Tiger mosquito
Biomarkers

sST2 as prognostic biomarker for severe dengue in adult patients

May 2, 2024
Researchers from Tan Tock Seng Hospital presented data from a study investigating the utility of soluble suppressor of tumorigenicity-2 (sST2) as early prognostic biomarker of severe dengue.
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Illustration of tick penetrating skin into blood stream
Biomarkers

MCP-3 predicts prognosis of severe fever with thrombocytopenia syndrome

April 30, 2024
Severe fever with thrombocytopenia syndrome (SFTS) is a tick-borne disease that results from an infection with the SFTS virus, with a case fatality rate of 6.1% to 21.8%. Identifying critically ill patients at the early stages is crucial for clinical management.
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Biomarkers

CD169 is a diagnostic marker of West Nile virus infection

April 29, 2024
About 25% of subjects with West Nile virus (WNV) infection develop fever and about 1% have neuroinvasive disease. Recent research has proposed measuring CD169 in peripheral blood (monocyte/lymphocyte ratio) as a marker of viral infections. The usefulness of monocyte CD169 (mCD169) in peripheral blood was tested in subjects with active WNV infection.
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Lymph nodes
Biomarkers

ZNF334 down-regulation linked to lymph node metastasis in lung squamous cell carcinoma

April 24, 2024
Lung cancer is still among the deadliest cancers worldwide, with squamous cell carcinoma (SCC) of the lung accounting for about 30% of the cases. When the cancer metastasizes to the lymph nodes, the patient has a worse overall survival.
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Medically accurate illustration of a baby in the womb of a pregnant mother
Cardiovascular

Peripartum cardiomyopathy is associated with placental senescence

April 24, 2024
By Mar de Miguel
Scientists at Massachusetts General Hospital have linked the risk of heart failure during pregnancy and senescence proteins produced by placental aging, which could clarify how peripartum cardiomyopathy (PPCM) is triggered and opens the door to the development of cardiac function therapies in late pregnancy.
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DNA sequencing
Biomarkers

Mutation in DAAM2 causes steroid-resistant nephrotic syndrome

April 19, 2024
Steroid-resistant nephrotic syndrome (SRNS) is a disease characterized by hypoalbuminemia, proteinuria, edema and hyperlipidemia, and a cause of chronic kidney disease in the pediatric population.
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Illustration of kidney with DNA structures
Biomarkers

Mutation in the UMOD gene tied to autosomal dominant tubulointerstitial kidney disease

April 18, 2024
Unknown etiology is commonly encountered in the kidney pre-transplant routine program. A screening program was performed to detect patients and study recipients that meet the following features: hypertension with no clear etiology and biopsies that do not match with clinical features of classical glomerulopathies.
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