Publications by authors named "Takashi Y"

Background: In patients with chronic kidney disease (CKD), fibroblast growth factor (FGF)-23 is suspected to cause death or cardiovascular disease by inducing left ventricular hypertrophy (LVH).

Objectives: This study aims to quantify the mediational effect of LVH in the hypothetical causal pathway from FGF-23 to long-term adverse outcomes.

Methods: From 3,939 adults with CKD stages 2 to 4 enrolled in the CRIC (Chronic Renal Insufficiency Cohort) study, 2,368 participants with available data of FGF-23, left ventricular mass index at 1 year, and covariates were included.

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Aim: To conduct a post hoc subgroup analysis of patients with type 2 diabetes (T2D) from the RECAP study, who were treated with sodium-glucose cotransporter-2 (SGLT2) inhibitor and glucagon-like peptide 1 receptor agonist (GLP-1RA) combination therapy, focusing only on those patients who had chronic kidney disease (CKD), to examine whether the composite renal outcome differed between those who received SGLT2 inhibitor treatment first and those who received a GLP-1RA first.

Methods: We included 438 patients with CKD (GLP-1RA-first group, n = 223; SGLT2 inhibitor-first group, n = 215) from the 643 T2D patients in the RECAP study. The incidence of the composite renal outcome, defined as progression to macroalbuminuria and/or a ≥50% decrease in estimated glomerular filtration rate (eGFR), was analysed using a propensity score (PS)-matched model.

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Purpose Of Review: Fibroblast growth factor 23 (FGF23) is a hormone to reduce blood phosphate concentration. Excessive actions of FGF23 induce FGF23-related hypophosphatemic disorders, such as X-linked hypophosphatemic rickets (XLH) and tumor-induced osteomalacia (TIO). We will summarize recent advances in the diagnosis and treatment of FGF23-related hypophosphatemic disorders.

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  • SGLT2 inhibitors (SGLT2i) and GLP-1 receptor agonists (GLP1Ra) both show protective effects for patients with diabetic kidney disease, often used in combination for type 2 diabetes (T2D).
  • A study involving 643 T2D patients examined differences in annual eGFR decline based on whether patients started with SGLT2i or GLP1Ra.
  • Results indicated that those starting with SGLT2i had a significantly smaller decline in eGFR after adding GLP1Ra, while the reverse pairing showed no significant change, suggesting the preceding drug influences the renal benefits of the combination therapy.
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Bone secrets the hormone, fibroblast growth factor 23 (FGF23), as an endocrine organ to regulate blood phosphate level. Phosphate is an essential mineral for the human body, and around 85% of phosphate is present in bone as a constituent of hydroxyapatite, Ca(PO)(OH). Because hypophosphatemia induces rickets/osteomalacia, and hyperphosphatemia results in ectopic calcification, blood phosphate (inorganic form) level must be regulated in a narrow range (2.

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  • Synthetic glucocorticoids (GCs) are widely used for treating autoimmune diseases but can lead to glucocorticoid-induced osteoporosis (GIOP), which significantly impacts patient quality of life and leads to fractures in many patients.
  • In 2014, the Japanese Society for Bone and Mineral Research established treatment guidelines for managing GIOP, using risk factors like age and bone density to determine appropriate therapy for patients on GC treatment for over three months.
  • The updated 2023 guidelines recommend starting osteoporosis medications, such as bisphosphonates and anti-RANKL antibodies, alongside GC therapy for high-risk patients to help prevent fractures.
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Excessive actions of FGF23 cause several kinds of hypophosphatemic rickets/osteomalacia. It is possible that there still remain unknown causes or mechanisms for FGF23-related hypophosphatemic diseases. We report two male cousins who had been suffering form FGF23-related hypophosphatemic osteomalacia.

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  • A study evaluated the effects of the order in which patients received sodium-glucose cotransporter inhibitors (SGLT2is) and GLP-1 receptor agonists (GLP1Ras) on kidney health in type 2 diabetes patients.
  • Researchers analyzed data from 643 patients who underwent at least one year of treatment and assessed kidney function based on albuminuria status and glomerular filtration rate (eGFR).
  • The findings indicated no significant difference in kidney outcomes between those who started with SGLT2is vs. GLP1Ras, suggesting that the sequence of medication administration does not impact renal health.
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Patients with neurological diseases, such as schizophrenia, tend to show low K-Cl co-transporter 2 (KCC2) levels in the brain. The cause of these diseases has been associated with stress and neuroinflammation. However, since the pathogenesis of these diseases is not yet fully investigated, drug therapy is still limited to symptomatic therapy.

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  • The study introduces "System-F," a device designed to effectively deliver vascular plugs to aortic side branches during endovascular aneurysm repair (EVAR).
  • It features a combination of specialized sheaths and a guidewire that allows for multidimensional movement, facilitating precise placement of vascular plugs in various arteries.
  • The results showed no occurrences of type II endoleak in the 7 cases treated, suggesting that System-F could enhance pre-EVAR embolization strategies and improve clinical outcomes.
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Background: Radiographic detection of the Adamkiewicz artery (AKA) before aortic surgery helps to avoid spinal cord ischemia (SCI). We applied magnetic resonance angiography (MRA) using gadolinium enhancement (Gd-MRA) by means of the slow-infusion method with sequential k-space filling and compared AKA detectability with that of computed tomography angiography (CTA).

Methods: A total of 63 patients with thoracic or thoracoabdominal aortic disease (30 with aortic dissection [AD] and 33 with aortic aneurysm) who underwent both CTA and Gd-MRA to detect AKA were evaluated.

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  • Tumor-induced osteomalacia (TIO) is often caused by phosphaturic mesenchymal tumors (PMTs), and complete tumor removal can cure TIO, but locating these tumors preoperatively is difficult using standard imaging methods.
  • The study evaluated the effectiveness of different imaging techniques—FDG-PET, SRS, and FGF23 venous sampling (FGF23VS)—in successfully localizing PMTs in patients with TIO.
  • Results showed that combining FDG-PET with FGF23VS achieved a 100% localization rate for PMTs, highlighting the importance of using multiple imaging methods for accurate diagnosis.
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Introduction: X-linked hypophosphatemia (XLH) is the most prevalent type of heritable fibroblast growth factor 23 (FGF23)-related hypophosphatemic rickets. Recently, anti-FGF23 antibody, burosumab, has become clinically available. We herein report a patient with adult XLH and tertiary hyperparathyroidism.

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  • Exercise loads the bone, likely causing it to release signals that communicate with fat tissue.
  • Systemic deletion of Interleukin-11 (IL-11) leads to lower bone mass, decreased bone formation with mechanical loading, and increased fat and glucose issues.
  • Specifically deleting IL-11 in bone cells affects bone health and fat levels, while deletion in fat cells shows no negative effects, highlighting the role of IL-11 in bone and fat regulation.
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This study aimed to evaluate the nitrogen removal of a post-treatment system for natural rubber processing wastewater (NRPW) under low chemical oxygen demand to total nitrogen (COD/TN) ratios without any supplemental external carbon source. The system including a downflow hanging sponge (DHS) reactor and an upflow anaerobic reactor (UAR) was operated in two phases. In phase 1 (day 0-102), under a nitrogen loading rate (NLR) of 0.

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Diabetic kidney disease (DKD) is a key determinant of morbidity and mortality in patients with type 1 diabetes (T1D). Identifying factors associated with early glomerular filtration rate (GFR) decline in T1D is important in prevention or early intervention for DKD. This study investigated whether phosphate metabolism, including fibroblast growth factor 23 (FGF23) is associated with the kidney function of patients with T1D.

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This study aimed to develop a simplified model for predicting end-stage kidney disease (ESKD) in patients with diabetes. The cohort included 2549 individuals who were followed up at Kyushu University Hospital (Japan) between January 1, 2008 and December 31, 2018. The outcome was a composite of ESKD, defined as an eGFR < 15 mL min [1.

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The Aging Males' Symptoms (AMS) score, developed to screen for late-onset hypogonadism (LOH), contains 17 questions regarding mental, physical, and sexual parameters. In the Japanese guidelines, a free testosterone (FT) <8.5 pg/mL is recommended for testosterone treatment.

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  • Researchers have previously used methods like digital droplet PCR and next-generation sequencing to measure pancreatic β-cell injury through unmethylation of the insulin gene, but these approaches have drawbacks such as needing specialized equipment and dealing with background noise.
  • A new technique was developed using two-step amplification refractory mutation system PCR to detect unmethylated insulin gene CpG sites in both type 1 diabetes patients and healthy individuals.
  • This new method demonstrated the ability to detect low levels of unmethylated insulin DNA effectively and showed an inverse relationship between DNA copy number and disease duration in patients, suggesting it could help monitor β-cell dynamics in conditions like type 1 diabetes.
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In recent years, conjugated microporous polymers (CMPs) have become important precursors for environmental and energy applications, compared with inorganic electrode materials, due to their ease of preparation, facile charge storage process, π-conjugated structures, relatively high thermal and chemical stability, abundance in nature, and high surface areas. Therefore, in this study, we designed and prepared new benzobisthiadiazole (BBT)-linked CMPs (BBT-CMPs) using a simple Sonogashira couplings reaction by reaction of 4,8-dibromobenzo(1,2-c;4,5-c')bis(1,2,5)thiadiazole (BBT-Br) with ethynyl derivatives of triphenylamine (TPA-T), pyrene (Py-T), and tetraphenylethene (TPE-T), respectively, to afford TPA-BBT-CMP, Py-BBT-CMP, and TPE-BBT-CMP. The chemical structure and properties of BBT-CMPs such as surface areas, pore size, surface morphologies, and thermal stability using different measurements were discussed in detail.

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The blood level of phosphate is tightly regulated in a narrow range. Hyperphosphatemia and hypophosphatemia both lead to the development of diseases, such as hyperphosphatemic tumoral calcinosis and rickets/osteomalacia, respectively. Although several humoral factors have been known to affect blood phosphate levels, fibroblast growth factor 23 (FGF23) is the principal hormone involved in the regulation of blood phosphate.

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Bone contributes to supporting the body, protecting the central nervous system and other organs, hematopoiesis, the regulation of mineral metabolism (mainly calcium and phosphate), and assists in respiration. Bone has many functions in the body. Recently, it was revealed that bone also works as an endocrine organ and secretes several systemic humoral factors, including fibroblast growth factor 23 (FGF23), osteocalcin (OC), sclerostin, and lipocalin 2.

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Due to its rarity, adrenal hemorrhage is difficult to diagnose, and its precise etiology has remained unknown. One of the pivotal mechanisms of adrenal hemorrhage is the thrombosis of the adrenal vein, which could be due to thrombophilia. However, detailed pathological evaluation of resected adrenal glands is usually required for definitive diagnosis.

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Diabetic kidney disease (DKD) is a major cause of end-stage kidney disease (ESKD) worldwide. Mineralocorticoid receptor (MR) plays an important role in the development of DKD. A series of preclinical studies revealed that MR is overactivated under diabetic conditions, resulting in promoting inflammatory and fibrotic process in the kidney.

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Purpose Of Review: X-linked hypophosphatemia and tumor-induced osteomalacia are diseases characterized by hypophosphatemia with impaired proximal tubular phosphate reabsorption. Complete resection of responsible tumors is the first-line therapy for patients with tumor-induced osteomalacia. In contrast, phosphate and active vitamin D have been used for patients with X-linked hypophosphatemia and inoperable ones with tumor-induced osteomalacia.

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