Protein Losing Nephropathy -- Glomerular Disease
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Genetically Determined Hypoalbuminemia As a Risk Factor for Hypertension: Instrumental Variable Analysis Jong Wook Choi1, Joon‑Sung Park2* & Chang Hwa Lee2*
www.nature.com/scientificreports OPEN Genetically determined hypoalbuminemia as a risk factor for hypertension: instrumental variable analysis Jong Wook Choi1, Joon‑Sung Park2* & Chang Hwa Lee2* Hypoalbuminemia is associated with vascular endothelial dysfunction and the development of chronic cardiovascular diseases. However, the relationship between serum albumin concentration and blood pressure changes remains controversial. Community‑based longitudinal cohort data collected from Korean Genome and Epidemiology Study were used in this study. Hypoalbuminemia was defned as a serum albumin concentration of ≤ 4.0 g/dL. A total of 4325 participants were categorized into control (n = 3157) and hypoalbuminemia (n = 1168) groups. Serum albumin had a non‑linear relationship with the risk of hypertension development. A genome‑wide association study revealed 71 susceptibility loci associated with hypoalbuminemia. Among susceptibility loci, genetic variations at rs2894536 in LOC107986598 and rs10972486 in ATP8B5P were related to elevated blood pressure. Serum albumin (HR = 0.654, 95% CI 0.521–0.820) and polymorphisms of rs2894536 (HR = 1.176, 95% CI 1.015–1.361) and rs10972486 (HR = 1.152, 95% CI 1.009–1.316) were signifcant predictors of hypertension development. Increased albumin concentration instrumented by 2 hypoalbuminemia‑associated SNPs (rs2894536 and rs10972486) was associated with decreased HRs for hypertension development (HR = 0.762, 95% CI 0.659–0.882 and HR = 0.759, 95% CI 0.656–0.878). Our study demonstrated that genetically determined hypoalbuminemia is a signifcant predictor of incipient hypertension. Albumin, one of the major serum proteins, has multiple important physiological functions involving stabilization of plasma colloid osmotic pressure, transportation of diverse substances, and signifcant antioxidant activity, and its concentration is fnely regulated by various systems in the physiologic state 1. -
Glycated Hemoglobin and Glycated Albumin in Patients with Diabetes
Kitajima et al. Renal Replacement Therapy (2020) 6:10 https://doi.org/10.1186/s41100-020-0260-5 RESEARCH Open Access Glycated hemoglobin and glycated albumin in patients with diabetes undergoing hemodiafiltration Yukie Kitajima1*, Shunichiro Urabe2, Takashi Hosono2, Satoshi Yoshikawa3, Yuzuru Sato3 and Toru Hyodo2 Abstract Background: Online hemodiafiltration (OHDF), which results in high albumin leakage, is now widely used in Japan for dialysis, since the national insurance system began reimbursing its costs in 2012. Glycated albumin (GA) levels are affected by albumin leakage into effluent dialysate fluid. Therefore, GA levels in patients requiring diabetes- related dialysis undergoing OHDF require monitoring. However, there have been no previous reports on glycemic control indicators of patients with diabetes undergoing OHDF. We aimed to develop a glycemic control index for patients requiring diabetes-related dialysis undergoing OHDF. Methods: This study comprised 133 diabetic patients undergoing OHDF. We examined the correlation between GA and glycated hemoglobin (HbA1c) levels. We analyzed effluent dialysate fluid samples from 41 patients classified into 3 groups, namely, group A, non-protein-leaking OHDF (n = 20); group B, protein-leaking OHDF (n = 14); and group C, highly efficient protein-leaking OHDF (n = 7). We examined the association between GA and HbA1c levels in each group and among patients. Results: A significant positive correlation was observed between GA and HbA1c levels (r = 0.562, p < 0.0001). There was no significant correlation between pre-dialysis blood glucose levels and HbA1c or GA levels as observed on regular blood tests performed under non-fasting conditions. Patients were classified into 2 groups based on their mean albumin levels (3.4 g/dL cutoff). -
Refractory Hypoglycemia in T-Cell Lymphoma
Open Access Austin Oncology Case Reports Case Report Refractory Hypoglycemia in T-Cell Lymphoma Buyukaydina B1*, Tunca M1, Alayb M2, Kazanciogluc R3 and Reha E3 Abstract 1Bezmialem Vakif University, Department of Internal Hypoglycemia is commonly seen in diabetes mellitus patients; whereas it Medicine, Turkey is rarely seen in a healthy person. In this case, we reported a male patient 2Yuzuncu Yil University, Department of Endocrinology, with a treatment-resistant hypoglycemia. A 53 years old male patient admitted Turkey to our clinic with debility, nausea and vomiting. Physical examination revealed 3Bezmialem Vakif University, Department of Nephology, lymphadenopathies in the left axilla and inguinal regions; and presence of right Turkey upper quadrant tenderness. Biochemical results revealed severe hypoglycemia, *Corresponding author: Banu Buyukaydin, azotemia and elevation of liver enzymes. Histological result of the excisional Bezmialem Vakif University, Department of Internal lymph node biopsy was compatible with peripheral T cell lymphoma. In ward, Medicine, Turkey the patient has repeated recurrent hypoglycemia, which did not resolve with all treatment given. His general condition deteriorated and he died due to sepsis. Received: June 01, 2016; Accepted: July 10, 2016; This case highlighted the need to rule out hematologic malignancies; precisely Published: July 13, 2016 T-cell lymphoma in a patient who presented with resistant hypoglycemia in the presence of lymphadenopathy. Keywords: Hypoglycemia, Lymphoma, IGF-II Introduction approximately fifty percent of proliferation index. CD3 was positive. This finding was compatible to histological diagnosis of peripheral Hypoglycemia is defined as the occurrence of a variety of T-cell lymphoma with partial involvement of lymph ganglia. symptoms in association with plasma glucose concentration of 50mg/dl or less. -
Clinical and Histopathological Features of Renal Maldevelopment in Boxer Dogs: a Retrospective Case Series (1999–2018) †
animals Article Clinical and Histopathological Features of Renal Maldevelopment in Boxer Dogs: A Retrospective Case Series (1999–2018) † Maria Alfonsa Cavalera 1, Floriana Gernone 1, Annamaria Uva 1, Paola D’Ippolito 2, Xavier Roura 3 and Andrea Zatelli 1,* 1 Department of Veterinary Medicine, University of Bari, 70010 Valenzano, Italy; [email protected] (M.A.C.); fl[email protected] (F.G.); [email protected] (A.U.) 2 Veterinary diagnostic Lab ACV Triggiano, 70019 Triggiano, Italy; [email protected] 3 Hospital Clínic Veterinari, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain; [email protected] * Correspondence: [email protected]; Tel.: +39-080-4679804 † This study was partially presented as oral communication at the 11th ECVIM-CA/ESVIM Congress, Dublin (Ireland) as “Congenital nephrotic syndrome with renal glomerular immaturity in 7 Boxer dogs”. Zatelli, A., Domenech, O., Bussadori, C., Lubas, G., Del Piero, F. Simple Summary: This study describes clinical findings in Boxer dogs with renal maldevelopment and proposes a possible mode of inheritance. Medical records of 9 female Boxer dogs, older than 5 months and with a clinical diagnosis of proteinuric chronic kidney disease prior to one year of age, showed the presence of polyuria and polydipsia, decreased appetite, weight loss, lethargy and weakness in all affected dogs. Common laboratory findings were proteinuria and diluted urine, non- regenerative anemia, azotemia, hyperphosphatemia, hypoalbuminemia and hypercholesterolemia. Citation: Cavalera, M.A.; Gernone, Histopathology of the kidneys identified the presence of immature glomeruli in all dogs. In 7 out F.; Uva, A.; D’Ippolito, P.; Roura, X.; of 9 related dogs, the pedigree analysis showed that a simple autosomal recessive trait may be a Zatelli, A. -
SIRS Is Valid in Discriminating Between Severe and Moderate Diabetic Foot Infections
Pathophysiology/Complications ORIGINAL ARTICLE SIRS Is Valid in Discriminating Between Severe and Moderate Diabetic Foot Infections 1 2 DANE K. WUKICH, MD KATHERINE MARIE RASPOVIC, DPM best of our knowledge, the use of SIRS 2 3 KIMBERLEE B. HOBIZAL, DPM BEDDA L. ROSARIO, PHD has not yet been validated as a method of discriminating between moderate and severe DFI. OBJECTIVEdThis retrospective, single-center study was designed to distinguish severe di- The aim of this study was to classify abetic foot infection (DFI) from moderate DFI based on the presence or absence of systemic fl infectionseverityinagroupofhospital- in ammatory response syndrome (SIRS). ized diabetic patients based on the pres- RESEARCH DESIGN AND METHODSdThe database of a single academic foot and ence or absence of SIRS. The reason for ankle program was reviewed and 119 patients were identified. Severe DFI was defined as local hospitalization in this group of patients infection associated with manifestation of two or more objective findings of systemic toxicity was their DFI. Our hypotheses are that using SIRS criteria. patients with DFI who manifest SIRS (i.e., severe infection) will have longer hospital RESULTSdPatients with severe DFI experienced a 2.55-fold higher risk of any amputation – – stays and higher rates of major amputa- (95% CI 1.21 5.36) and a 7.12-fold higher risk of major amputation (1.83 41.05) than patients tion than patients who don’tmanifest with moderate DFI. The risk of minor amputations was not significantly different between the two groups (odds ratio 1.02 [95% CI 0.51–2.28]). The odds of having a severe DFI was 7.82 SIRS (i.e., moderate infection). -
Increasing Ferritin Predicts Early Death in Adult Hemophagocytic Lymphohistiocytosis
Henry Ford Health System Henry Ford Health System Scholarly Commons Pathology Articles Pathology 2-17-2021 Increasing ferritin predicts early death in adult hemophagocytic lymphohistiocytosis Rand Abou Shaar Charles S. Eby Suzanne van Dorp Theo de Witte Zaher K. Otrock Follow this and additional works at: https://scholarlycommons.henryford.com/pathology_articles Received: 13 November 2020 | Accepted: 29 January 2021 DOI: 10.1111/ijlh.13489 ORIGINAL ARTICLE Increasing ferritin predicts early death in adult hemophagocytic lymphohistiocytosis Rand Abou Shaar1 | Charles S. Eby2 | Suzanne van Dorp3 | Theo de Witte3 | Zaher K. Otrock1 1Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, MI, Abstract USA Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome of 2 Department of Pathology and Immunology, pathologic immune activation. Most studies on adult HLH have evaluated prognostic Washington University School of Medicine, St. Louis, MO, USA factors for overall survival; factors predicting early mortality have not been suffi- 3Radboud University Medical Center, ciently investigated. Nijmegen, Netherlands Methods: This was a collaborative study between Henry Ford Hospital and Barnes- Correspondence Jewish Hospital. We identified all adult HLH patients with at least 2 ferritin levels Zaher K. Otrock, Transfusion Medicine Division, Department of Pathology and within 30 days from admission. Laboratory Medicine, Henry Ford Hospital, Results: One- hundred twenty- four patients were identified. There were -
Hypoalbuminemia at Admission Predicts the Development of Acute Kidney Injury in Hospitalized Patients: a Retrospective Cohort Study
RESEARCH ARTICLE Hypoalbuminemia at admission predicts the development of acute kidney injury in hospitalized patients: A retrospective cohort study Mi-yeon Yu1, Sung Woo Lee2, Seon Ha Baek3, Ki Young Na4, Dong-Wan Chae4, Ho Jun Chin4, Sejoong Kim4* 1 Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea, 2 Department of a1111111111 Internal Medicine, Eulji General Hospital, Seoul, Korea, 3 Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital, Gyeonggi-do, Korea, 4 Department of Internal Medicine, Seoul National a1111111111 University Bundang Hospital, Seongnam, Korea a1111111111 a1111111111 * [email protected] a1111111111 Abstract OPEN ACCESS Citation: Yu M-y, Lee SW, Baek SH, Na KY, Chae D-W, Chin HJ, et al. (2017) Hypoalbuminemia at Background admission predicts the development of acute Development of acute kidney injury (AKI) is common and is associated with poor outcomes. kidney injury in hospitalized patients: A We aimed to determine whether hypoalbuminemia (HA) at admission could be a risk factor retrospective cohort study. PLoS ONE 12(7): e0180750. https://doi.org/10.1371/journal. for the development of AKI and mortality in hospitalized patients. pone.0180750 Editor: Emmanuel A. Burdmann, University of Sao Paulo Medical School, BRAZIL Methods Received: March 14, 2017 We enrolled patients who were admitted to Seoul National University Bundang Hospital Accepted: June 20, 2017 from January 2013 to December 2013. HA at admission was defined as a serum albumin Published: July 19, 2017 level < 3.4 mg/dL measured within two days after admission. AKI was defined as an increase in the serum creatinine level by 0.3 mg/dL or 1.5 times of the baseline value Copyright: © 2017 Yu et al. -
Uremic Toxins Affect Erythropoiesis During the Course of Chronic
cells Review Uremic Toxins Affect Erythropoiesis during the Course of Chronic Kidney Disease: A Review Eya Hamza 1, Laurent Metzinger 1,* and Valérie Metzinger-Le Meuth 1,2 1 HEMATIM UR 4666, C.U.R.S, Université de Picardie Jules Verne, CEDEX 1, 80025 Amiens, France; [email protected] (E.H.); [email protected] (V.M.-L.M.) 2 INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), UFR SMBH, Université Sorbonne Paris Nord, CEDEX, 93017 Bobigny, France * Correspondence: [email protected]; Tel.: +33-2282-5356 Received: 17 July 2020; Accepted: 4 September 2020; Published: 6 September 2020 Abstract: Chronic kidney disease (CKD) is a global health problem characterized by progressive kidney failure due to uremic toxicity and the complications that arise from it. Anemia consecutive to CKD is one of its most common complications affecting nearly all patients with end-stage renal disease. Anemia is a potential cause of cardiovascular disease, faster deterioration of renal failure and mortality. Erythropoietin (produced by the kidney) and iron (provided from recycled senescent red cells) deficiencies are the main reasons that contribute to CKD-associated anemia. Indeed, accumulation of uremic toxins in blood impairs erythropoietin synthesis, compromising the growth and differentiation of red blood cells in the bone marrow, leading to a subsequent impairment of erythropoiesis. In this review, we mainly focus on the most representative uremic toxins and their effects on the molecular mechanisms underlying anemia of CKD that have been studied so far. Understanding molecular mechanisms leading to anemia due to uremic toxins could lead to the development of new treatments that will specifically target the pathophysiologic processes of anemia consecutive to CKD, such as the newly marketed erythropoiesis-stimulating agents. -
Glomerulonephritis Management in General Practice
Renal disease • THEME Glomerulonephritis Management in general practice Nicole M Isbel MBBS, FRACP, is Consultant Nephrologist, Princess Alexandra lomerular disease remains an important cause Hospital, Brisbane, BACKGROUND Glomerulonephritis (GN) is an G and Senior Lecturer in important cause of both acute and chronic kidney of renal impairment (and is the commonest cause Medicine, University disease, however the diagnosis can be difficult of end stage kidney disease [ESKD] in Australia).1 of Queensland. nikky_ due to the variability of presenting features. Early diagnosis is essential as intervention can make [email protected] a significant impact on improving patient outcomes. OBJECTIVE This article aims to develop However, presentation can be variable – from indolent a structured approach to the investigation of patients with markers of kidney disease, and and asymptomatic to explosive with rapid loss of kidney promote the recognition of patients who need function. Pathology may be localised to the kidney or further assessment. Consideration is given to the part of a systemic illness. Therefore diagnosis involves importance of general measures required in the a systematic approach using a combination of clinical care of patients with GN. features, directed laboratory and radiological testing, DISCUSSION Glomerulonephritis is not an and in many (but not all) cases, a kidney biopsy to everyday presentation, however recognition establish the histological diagnosis. Management of and appropriate management is important to glomerulonephritis (GN) involves specific therapies prevent loss of kidney function. Disease specific directed at the underlying, often immunological cause treatment of GN may require specialist care, of the disease and more general strategies aimed at however much of the management involves delaying progression of kidney impairment. -
The Links Between Microbiome and Uremic Toxins in Acute Kidney Injury: Beyond Gut Feeling—A Systematic Review
toxins Article The Links between Microbiome and Uremic Toxins in Acute Kidney Injury: Beyond Gut Feeling—A Systematic Review Alicja Rydzewska-Rosołowska 1,* , Natalia Sroka 1, Katarzyna Kakareko 1, Mariusz Rosołowski 2 , Edyta Zbroch 1 and Tomasz Hryszko 1 1 2nd Department of Nephrology and Hypertension with Dialysis Unit, Medical University of Białystok, 15-276 Białystok, Poland; [email protected] (N.S.); [email protected] (K.K.); [email protected] (E.Z.); [email protected] (T.H.) 2 Department of Gastroenterology and Internal Medicine, Medical University of Białystok, 15-276 Białystok, Poland; [email protected] * Correspondence: [email protected] Received: 30 October 2020; Accepted: 9 December 2020; Published: 11 December 2020 Abstract: The last years have brought an abundance of data on the existence of a gut-kidney axis and the importance of microbiome in kidney injury. Data on kidney-gut crosstalk suggest the possibility that microbiota alter renal inflammation; we therefore aimed to answer questions about the role of microbiome and gut-derived toxins in acute kidney injury. PubMed and Cochrane Library were searched from inception to October 10, 2020 for relevant studies with an additional search performed on ClinicalTrials.gov. We identified 33 eligible articles and one ongoing trial (21 original studies and 12 reviews/commentaries), which were included in this systematic review. Experimental studies prove the existence of a kidney-gut axis, focusing on the role of gut-derived uremic toxins and providing concepts that modification of the microbiota composition may result in better AKI outcomes. Small interventional studies in animal models and in humans show promising results, therefore, microbiome-targeted therapy for AKI treatment might be a promising possibility. -
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www.jasn.org EDITORIALS 5. Grimm PR, Coleman R, Delpire E, Welling PA: Constitutively active Cachexia with muscle wasting is prevalent and closely associated SPAK causes hyperkalemia by activating NCC and remodeling distal with mortality and morbidity in patients with CKD.1 The patho- – tubules. JAmSocNephrol28: 2597 2606, 2017 physiology of muscle wasting in CKD is complex. Inadequate 6. Moriguchi T, Urushiyama S, Hisamoto N, Iemura S, Uchida S, Natsume T, Matsumoto K, Shibuya H: WNK1 regulates phosphorylation of cation- nutritional intake, physical inactivity from muscle weakness, sys- chloride-coupled cotransporters via the STE20-related kinases, SPAK temic inflammation and aberrant signaling of neuropeptides have and OSR1. J Biol Chem 280: 42685–42693, 2005 been implicated.2 To date, there is no effective therapy. Exercise 7. YangSS,MorimotoT,RaiT,ChigaM,SoharaE,OhnoM,UchidaK,LinSH, training has well documented health benefits, including mainte- Moriguchi T, Shibuya H, Kondo Y, SasakiS,UchidaS:Molecularpatho- nance of muscle mass as well as increased physical performance genesis of pseudohypoaldosteronism type II: Generation and analysis of a fi Wnk4(D561A/1) knockin mouse model. Cell Metab 5: 331–344, 2007 resulting from changes in muscle ber phenotype leading to in- 8. Lalioti MD, Zhang J, Volkman HM, Kahle KT, Hoffmann KE, Toka HR, Nelson- creased mitochondrial biogenesis. The molecular signaling mech- Williams C, Ellison DH, Flavell R, Booth CJ, Lu Y, Geller DS, Lifton RP: Wnk4 anism underlying adaptations to increased physical activity in controls blood pressure and potassium homeostasis via regulation of mass CKD-associated muscle wasting is not well understood. – and activity of the distal convoluted tubule. -
Mineralocorticoid-Resistant Renal Hyperkalemia Without Salt Wasting
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Kidney International, Vol. 19 (1981), pp. 716—727 Mineralocorticoid-resistant renal hyperkalemia without sal wasting (type II pseudohypoaldosteronism): Role of increased renal chloride reabsorption MORRIS SCHAMBELAN, ANTHONY SEBASTIAN, and FLOYD C. RECTOR, JR. Medical Service and Clinical Study Center, San Francisco General Hospital Medical Center, and the Department of Medicine, Cardiovascular Research Institute, and the General Clinical Research Center, University of California, San Francisco, California Mineralocorticoid-resistant renal hyperkalemia without salt Hyperkaliemie rénale resistant aux minéralocorticoides sans wasting (type II pseudohypoaldosteronism): Role of increased perte de sel (pseudohypoaldostéronisme de type II): Role de l'aug- renal chloride reabsorption. A rare syndrome has been described mentation iie Ia reabsorption de chlore. Un syndrome rare a été in which mineralocorticoid-resistant hyperkalemia of renal origin décrit dans lequel une hyperkaliemie d'origine rénale resistant occurs in the absence of glomerular insufficiency and renal aux minéralocorticoides survient en l'absence de diminution du sodium wasting and in which hyperchioremic acidosis, hyperten- debit de filtration glomerulaire et de perte rénale de sodium et sion, and hyporeninemia coexist. The primary abnormality has dans lequel une acidose hyperchioremique, une hypertension et been postulated to be a defect of the potassium secretory une hyporéninémie coexistent. L'anomalie primaire qui a été mechanism of the distal nephron. The present studies were postulée est un deficit du mécanisme de secretion de potassium carried out to investigate the mechanism of impaired renal du nephron distal. Ce travail a etC entrepris pour étudier le potassium secretion in a patient with this syndrome.