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1.
Medicina (Kaunas) ; 59(11)2023 Nov 17.
Article in English | MEDLINE | ID: mdl-38004073

ABSTRACT

Background and Objectives: The Wakayama prefecture is endemic for two types of tick-borne rickettsioses: Japanese spotted fever (JFS) and scrub typhus (ST). Severe fever with thrombocytopenia syndrome (SFTS) is a tick-borne hemorrhagic viral disease with a high mortality rate and is often difficult to differentiate from such rickettsioses. SFTS cases have recently increased in Wakayama prefecture. For early diagnosis, this study aimed to evaluate the clinical characterization of such tick-borne infections in the co-endemic area. Materials and Methods: The study included 64 febrile patients diagnosed with tick-borne infection in Wakayama prefecture between January 2013 and May 2022. Medical records of 19 patients with SFTS and 45 with rickettsiosis (JSF, n = 26; ST, n = 19) were retrospectively examined. The receiver operating curve (ROC) and area under the curve (AUC) were calculated to evaluate potential factors for differentiating SFTS from rickettsiosis. Results: Adults aged ≥70 years were most vulnerable to tick-borne infections (median, 75.5 years; interquartile range, 68.5-84 years). SFTS and rickettsiosis occurred mostly between summer and autumn. However, no significant between-group differences were found in age, sex, and comorbidities; 17 (89%) patients with SFTS, but none of those with rickettsiosis, experienced gastrointestinal symptoms such as vomiting, abdominal pain, and diarrhea. Meanwhile, 43 (96%) patients with rickettsiosis, but none of those with SFTS, developed a skin rash. The AUCs of white blood cells (0.97) and C-reactive protein (CRP) levels (0.98) were very high. Furthermore, the differential diagnosis of SFTS was significantly associated with the presence of gastrointestinal symptoms (AUC 0.95), the absence of a skin rash (AUC 0.98), leukopenia <3.7 × 109/L (AUC 0.95), and low CRP levels < 1.66 mg/dL (AUC 0.98) (p < 0.001 for each factor). Conclusions: Clinical characteristics and standard laboratory parameters can verify the early diagnosis of SFTS in areas where tick-borne infections are endemic.


Subject(s)
Exanthema , Phlebovirus , Rickettsia Infections , Scrub Typhus , Severe Fever with Thrombocytopenia Syndrome , Tick-Borne Diseases , Adult , Humans , Severe Fever with Thrombocytopenia Syndrome/diagnosis , Severe Fever with Thrombocytopenia Syndrome/epidemiology , Retrospective Studies , Japan/epidemiology , Rickettsia Infections/diagnosis , Rickettsia Infections/epidemiology , Scrub Typhus/complications , Scrub Typhus/diagnosis , Scrub Typhus/epidemiology , Tick-Borne Diseases/diagnosis
2.
Semin Dial ; 31(5): 519-527, 2018 09.
Article in English | MEDLINE | ID: mdl-29738093

ABSTRACT

Acute kidney injury (AKI) is one of the most common serious complications for all hospital admissions, with its incidence increasing among hospitalized patients, particularly those in the intensive care unit. Despite significant improvements in critical care and dialysis technology, AKI is associated with an increased risk of short- and long-term mortality, prolonged hospital stays, and dialysis dependence. These risks are particularly relevant for critically ill patients with AKI severe enough to require renal replacement therapy (RRT). No specific pharmacologic treatment has been established to treat AKI. Hence, the mainstay treatment for patients with AKI is RRT even though there are still several problematic issues regarding its use including RRT modality, dose, and timing. Recently, the impact of AKI on an increased risk of progression to chronic kidney disease (CKD) and end-stage renal disease requiring dialysis or transplantation is attracting increased attention.


Subject(s)
Acute Kidney Injury/epidemiology , Renal Replacement Therapy/methods , Acute Kidney Injury/complications , Acute Kidney Injury/therapy , Cardiovascular Diseases/etiology , Critical Illness/mortality , Critical Illness/therapy , Humans , Incidence , Renal Insufficiency, Chronic/etiology , Risk Factors
3.
Intern Med ; 55(23): 3535-3538, 2016.
Article in English | MEDLINE | ID: mdl-27904124

ABSTRACT

An 82-year-old Japanese man, who presented with a fever and abdominal pain, was admitted to our hospital. According to enhanced computed tomography images, the probable diagnosis was abdominal aortic mycotic aneurysm. Eight sets of blood cultures obtained from the patient were negative. Despite administering treatment with vancomycin and ceftriaxone, the aneurysm progressively enlarged. He underwent open debridement surgery and in situ replacement because of an aneurysmal rupture. Bacteroides fragilis was isolated from the tissue culture of the aortic wall. Metronidazole was administered and discontinued without any infection relapse. When faced with similar cases, rare pathogens should thus be considered as possible causes of mycotic aneurysms.


Subject(s)
Aneurysm, Infected/diagnosis , Aortic Aneurysm, Abdominal/diagnosis , Bacteroides Infections/diagnosis , Bacteroides fragilis/isolation & purification , Immunocompromised Host , Aged, 80 and over , Aneurysm, Infected/microbiology , Aortic Aneurysm, Abdominal/microbiology , Bacteroides Infections/microbiology , Fatal Outcome , Humans , Male , Tomography, X-Ray Computed
4.
Growth Factors ; 34(5-6): 196-202, 2016 12.
Article in English | MEDLINE | ID: mdl-28095739

ABSTRACT

The FGF23-Klotho signaling axis is known to exert anti-aging effects via calcium-phosphorus metabolism. In mice deficient in FGF23-Klotho signaling, however, the number of splenocytes is reduced. FGF23 is expressed in both bone and spleen, with regulation of its production differing in these organs. As FGF23-Klotho signaling may play an immunological role in the spleen, splenocytes in male C57BL/6J mice were assayed for expression of Klotho or FGF23 by flow cytometry and immunohistochemistry. Cells that expressed Klotho included CD45R/B220+ CD21/CD35+ CD1d+ CD43- marginal zone B cells. These cells also expressed FGF receptor 1, indicating that Klotho-positive B cells could respond to FGF23. Plasmacytoid dendritic cells (pDCs) with CD11c+ CD45R/B220+ CD11b- CD8α- were found to produce FGF23. Klotho-positive cells and FGF23-producing cells were present in close proximity to each other, suggesting that FGF23 produced by pDCs may act within a limited area. These findings indicate that FGF23-Klotho signaling could play a biological or immunological role in the spleen.


Subject(s)
Fibroblast Growth Factors/metabolism , Glucuronidase/metabolism , Spleen/metabolism , Animals , B-Lymphocytes/metabolism , Dendritic Cells/metabolism , Fibroblast Growth Factor-23 , Fibroblast Growth Factors/genetics , Glucuronidase/genetics , Klotho Proteins , Male , Mice , Mice, Inbred C57BL , Receptors, Fibroblast Growth Factor/genetics , Receptors, Fibroblast Growth Factor/metabolism , Spleen/cytology
5.
Intern Med ; 54(17): 2207-11, 2015.
Article in English | MEDLINE | ID: mdl-26328648

ABSTRACT

A 29-year-old woman was diagnosed with Henoch-Schönlein purpura nephritis (HSPN) based on the presence of purpura and histopathological findings showing crescent formation, mesangial proliferation and IgA deposition in the glomerular mesangium. She was treated with high-dose steroids; however, the nephritic syndrome persisted. Therefore, we diagnosed her with steroid-resistant HSPN and decided to add treatment with cyclosphamide pulse therapy. After one year of treatment, the histopathological findings, including crescent formation and IgA deposition, improved, as confirmed on a renal biopsy, and the patient fulfilled the criteria for complete remission. Cyclophosphamide pulse therapy may be considered an effective treatment for intractable HSPN.


Subject(s)
Cyclophosphamide/administration & dosage , IgA Vasculitis/drug therapy , Immunosuppressive Agents/administration & dosage , Nephritis/pathology , Pulse Therapy, Drug , Steroids/administration & dosage , Adult , Cyclophosphamide/adverse effects , Female , Heart Rate , Humans , IgA Vasculitis/pathology , Immunosuppressive Agents/adverse effects , Monitoring, Physiologic , Nephritis/immunology , Remission Induction , Treatment Outcome
8.
Clin Calcium ; 22(10): 1557-66, 2012 Oct.
Article in Japanese | MEDLINE | ID: mdl-23023637

ABSTRACT

Hyperphosphatemia is the most common complication among patients with chronic kidney disease. Large scale observational studies have identified hyperphosphatemia as an independent risk factor for cardiovascular disease and mortality in hemodialysis patients. The combination therapy of dietary phosphate restriction and phosphate removal with dialysis treatment is still not enough to achieve the serum phosphate within the target. Thererfore, phosphate binders is necessary for many dialyzed patients with hyperphosphatemia. In this article, we will review the detail and development of phosphate binders and recommendation for clinical practice in hyperphosphatemia.


Subject(s)
Hyperphosphatemia/therapy , Phosphates/metabolism , Renal Insufficiency, Chronic/therapy , Chelating Agents/therapeutic use , Humans , Hyperphosphatemia/complications , Kidney/metabolism , Kidney/physiopathology , Phosphates/analysis , Phosphates/chemistry , Renal Dialysis
9.
Article in English | MEDLINE | ID: mdl-22723728

ABSTRACT

Hyperphosphatemia has been shown to be involved not only in the onset and progression of secondary hyperparathyroidism but also in vascular calcification. In addition, it influences the clinical course of patients with chronic kidney disease. Phosphate (Pi) binder is required in the management of hyperparaphosphatemia, because dietary Pi restriction and Pi removal by hemodialysis alone are insufficient. Lanthanum carbonate, a powerful Pi binder, has a similar effect to aluminum hydroxide in reducing serum Pi levels. As it is excreted via the liver, lanthanum carbonate has an advantage in patients with renal failure. The effect of lanthanum carbonate on serum Pi levels is almost two times higher than that of calcium (Ca) carbonate, which is commonly used. Lanthanum carbonate and Ca carbonate have an additive effect. Worldwide, there is 6 years worth of clinical treatment data on lanthanum carbonate; however, we have 3 years of clinical use in Japanese patients with hyperphosphatemia. No serious side effects have been reported. However, the most important concern is bone toxicity, which has been observed with use of aluminum hydroxide. For this study, clinical research involved analysis of bone biopsies. Although osteomalacia is the most noticeable side effect, this was not observed. Both the high- and the low-turnover bone disease concentrated into a normal bone turnover state. However, as the authors have less than 10 years' clinical experience with lanthanum carbonate, patients should be monitored carefully. In addition, it is necessary to demonstrate whether potent treatment effects on hyperphosphatemia improve the long-term outcome.

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