keyword
https://read.qxmd.com/read/38600408/sprayed-urine-emits-a-pungent-odor-due-to-its-increased-adhesion-to-vertical-objects-via-urinary-proteins-rather-than-to-changes-in-its-volatile-chemical-profile-in-domestic-cats
#21
JOURNAL ARTICLE
Reiko Uenoyama, Wenrui Zhu, Makoto Miura, Tamako Miyazaki, Masao Miyazaki
Spraying urine on vertical objects by raising the tail is a commonly observed functional behavior for chemical communication in Felidae species, including domestic cats (Felis silvestris catus). The sprayed urine is recognized as a chemical signal for territorial ownership of their habitats. Previous studies reported that sprayed urine emits a more pungent odor than urine excreted from a squatting position. However, little is known about how sprayed urine acts as a strong scent mark in the environment. Here, we showed that sprayed urine originates only from bladder urine without any secretions, such as anal sac secretions, but it can effectively emit volatile organic compounds (VOCs) when smeared on vertical objects due to its strong adhesion...
April 10, 2024: Journal of Chemical Ecology
https://read.qxmd.com/read/38596443/bcd020-rituximab-bioanalog-compared-to-standard-treatment-in-juvenile-systemic-lupus-erythematosus-the-data-of-12-months-case-control-study
#22
JOURNAL ARTICLE
Elvira Kalashnikova, Eugenia Isupova, Ekaterina Gaidar, Lyubov Sorokina, Maria Kaneva, Vera Masalova, Margarita Dubko, Tatiana Kornishina, Natalia Lubimova, Ekaterina Kuchinskaya, Irina Chikova, Rinat Raupov, Olga Kalashnikova, Mikhail Kostik
BACKGROUND: Systemic lupus erythematosus (SLE) is the most frequent and serious systemic connective tissue disease. Nowadays there is no clear guidance on its treatment in childhood. There are a lot of negative effects of standard-of-care treatment (SOCT), including steroid toxicity. Rituximab (RTX) is the biological B-lymphocyte-depleting agent suggested as a basic therapy in pediatric SLE. AIM: To compare the benefits of RTX above SOCT. METHODS: The data from case histories of 79 children from the Saint-Petersburg State Pediatric Medical University from 2012 to 2022 years, were analyzed...
March 9, 2024: World Journal of Clinical Pediatrics
https://read.qxmd.com/read/38596269/exploring-kidney-biopsy-findings-in-congenital-heart-diseases-insights-beyond-cyanotic-nephropathy
#23
JOURNAL ARTICLE
Jose Daniel Juarez-Villa, Iván Zepeda-Quiroz, Sebastián Toledo-Ramírez, Victor Hugo Gomez-Johnson, Francisco Pérez-Allende, Brian Ricardo Garibay-Vega, Francisco E Rodríguez Castellanos, Bernardo Moguel-González, Edgar Garcia-Cruz, Salvador Lopez-Gil
BACKGROUND: The association between congenital heart disease and chronic kidney disease is well known. Various mechanisms of kidney damage associated with congenital heart disease have been established. The etiology of kidneydisease has commonly been considered to be secondary to focal segmental glomerulosclerosis (FSGS), however, this has only been demonstrated in case reports and not in observational or clinical trials. AIM: To identify baseline and clinical characteristics, as well as the findings in kidney biopsies of patients with congenital heart disease in our hospital...
March 25, 2024: World Journal of Nephrology
https://read.qxmd.com/read/38596093/traditional-chinese-medicine-for-idiopathic-membranous-nephropathy-a-systematic-review-and-meta-analysis
#24
JOURNAL ARTICLE
Wenjun Shan, Haiyu Guan, Haowen Gu, Rongrong Wang, Xiaoyan Huang, Ping Li, Ying Xie, Kun Bao, Xindong Qin
BACKGROUND: Idiopathic membranous nephropathy (IMN) is a rare autoimmune disorder that causes nephrotic syndromes in adults. Conventional immunosuppressive therapies often exhibit limited efficacy in achieving remission and may result in notable adverse reactions, warranting the exploration of novel therapeutic approaches for IMN treatment. Traditional Chinese medicine (TCM), which is extensively used for kidney disease management, is a promising alternative. OBJECTIVE: This study aimed to examine the safety and efficacy of TCM alone or in combination with Western medicine for the management of patients diagnosed with IMN...
April 15, 2024: Heliyon
https://read.qxmd.com/read/38595244/-low-disease-activity-and-remission-status-of-systemic-lupus-erythematosus-in-a-real-world-study
#25
JOURNAL ARTICLE
Limin Ren, Chuchu Zhao, Yi Zhao, Huiqiong Zhou, Liyun Zhang, Youlian Wang, Lingxun Shen, Wenqiang Fan, Yang Li, Xiaomei Li, Jibo Wang, Yongjing Cheng, Jiajing Peng, Xiaozhen Zhao, Miao Shao, Ru Li
OBJECTIVE: To investigate the rates of low disease activity and clinical remission in patients with systemic lupus erythematosus (SLE) in a real-world setting, and to analyze the related factors of low disease activity and clinical remission. METHODS: One thousand patients with SLE were enrolled from 11 teaching hospitals. Demographic, clinical and laboratory data, as well as treatment regimes were collec-ted by self-completed questionnaire. The rates of low disease activity and remission were calculated based on the lupus low disease activity state (LLDAS) and definitions of remission in SLE (DORIS)...
April 18, 2024: Beijing da Xue Xue Bao. Yi Xue Ban, Journal of Peking University. Health Sciences
https://read.qxmd.com/read/38591825/percutaneous-kidney-biopsies-in-children-a-24-year-review-in-a-tertiary-center-in-northern-portugal
#26
JOURNAL ARTICLE
Patrícia Sousa, Catarina Brás, Catarina Menezes, Ramon Vizcaino, Teresa Costa, Maria Sameiro Faria, Conceição Mota
INTRODUCTION: Percutaneous kidney biopsy (KB) is crucial to the diagnosis and management of several renal pathologies. National data on native KB in pediatric patients are scarce. We aimed to review the demographic and clinical characteristics and histopathological patterns in children who underwent native percutaneous KB over 24 years. METHODS: Retrospective observational study of patients undergoing native percutaneous KB in a pediatric nephrology unit between 1998 and 2021, comparing 3 periods: period 1 (1998-2005), period 2 (2006-2013), and period 3 (2014-2021)...
2024: Jornal Brasileiro de Nefrologia: ʹorgão Oficial de Sociedades Brasileira e Latino-Americana de Nefrologia
https://read.qxmd.com/read/38591291/clinicopathological-features-and-outcome-of-secondary-steroid-resistant-nephrotic-syndrome-a-retrospective-analysis
#27
JOURNAL ARTICLE
Habib Qaiser, Irshad Bajeer, Sabeeta Khatri, Seema Hashmi, Ali Asghar Lanewala
OBJECTIVE: To determine the clinico-pathological features and long-term outcome of secondary steroid-resistant nephrotic syndrome treated with steroids and calcineurin inhibitors. METHODS: The retrospective cohort study was conducted at the Sindh Institute of Urology and Transplant, Karachi, in June and July 2023, and comprised data from January 1, 2008, to December 31, 2020, of children aged 1-18 years who developed steroid resistance after initial sensitivity to steroids with at least 1-year of follow-up...
March 2024: JPMA. the Journal of the Pakistan Medical Association
https://read.qxmd.com/read/38590565/proteinase%C3%A2-3%C3%A2-antineutrophil-cytoplasmic-antibody%C3%A2-associated-vasculitis-secondary-to-subacute-infective-endocarditis-a-case-report
#28
Hui Lu, Zhao Cui, Xu-Jie Zhou, Ying Yang, Xiao-Ning Han, Xi-Hui Li, Fu-De Zhou, Ming-Hui Zhao
A 58-year-old male patient was admitted to Peking University First Hospital (Beijing, China) due to recurrent hematuria, proteinuria and kidney dysfunction. The patient was positive for proteinase-3 (PR3)-antineutrophil cytoplasmic antibody (ANCA). Pathology of the kidney showed focal proliferative necrotizing glomerulonephritis with crescent formation and immune complex-mediated glomerulonephritis. The patient was diagnosed with PR3-ANCA-associated vasculitis (AAV), received intensive immunosuppressive therapy and experienced two relapses within 1 year...
May 2024: Experimental and Therapeutic Medicine
https://read.qxmd.com/read/38589766/nephronophthisis-13-caused-by-wdr19-variants-with-pancytopenia-case-report
#29
JOURNAL ARTICLE
Yu Tanaka, Tomoko Horinouchi, Yuta Inoki, Yuta Ichikawa, Chika Ueda, Hideaki Kitakado, Atsushi Kondo, Nana Sakakibara, China Nagano, Yoshihiko Yano, Norishige Yoshikawa, Naoya Morisada, Kandai Nozu
We present a case of nephronophthisis 13 that resulted from WDR19 variants. The patient, a nine-year-old Japanese boy, had detection of mild proteinuria during a school urine screening. Urinalysis revealed mild proteinuria without hematuria. Blood tests indicated pancytopenia, mild elevation of liver enzymes, and kidney dysfunction. Ultrasound examination disclosed hepatosplenomegaly. Abdominal computed tomography and bone marrow assessments ruled out malignant tumors. Subsequent kidney and liver biopsies suggested nephronophthisis and congenital hepatic fibrosis...
April 8, 2024: CEN Case Reports
https://read.qxmd.com/read/38589699/outcome-10%C3%A2-years-after-shiga-toxin-producing-e-coli-stec-associated-hemolytic-uremic-syndrome-importance-of-long-term-follow-up
#30
JOURNAL ARTICLE
Alejandra Rosales, Sarah Kuppelwieser, Thomas Giner, Johannes Hofer, Magdalena Riedl Khursigara, Dorothea Orth-Höller, Wegene Borena, Gerard Cortina, Therese Jungraithmayr, Reinhard Würzner
BACKGROUND: Hemolytic uremic syndrome (HUS) is an important cause of acute kidney injury in children. HUS is known as an acute disease followed by complete recovery, but patients may present with kidney abnormalities after long periods of time. This study evaluates the long-term outcome of Shiga toxin-producing Escherichia coli-associated HUS (STEC-HUS) in pediatric patients, 10 years after the acute phase of disease to identify risk factors for long-term sequelae. METHODS: Over a 6-year period, 619 patients under 18 years of age with HUS (490 STEC-positive, 79%) were registered in Austria and Germany...
April 9, 2024: Pediatric Nephrology
https://read.qxmd.com/read/38589698/atypical-phenotypes-and-novel-ocrl-variations-in-southern-chinese-patients-with-lowe-syndrome
#31
JOURNAL ARTICLE
Rong Du, Chengcheng Zhou, Shehong Chen, Tong Li, Yunting Lin, Aijing Xu, Yonglan Huang, Huifen Mei, Xiaoli Huang, Dongdong Tan, Ruidan Zheng, Cuili Liang, Yanna Cai, Yongxian Shao, Wen Zhang, Li Liu, Chunhua Zeng
BACKGROUND: Lowe syndrome is characterized by the presence of congenital cataracts, psychomotor retardation, and dysfunctional proximal renal tubules. This study presents a case of an atypical phenotype, investigates the genetic characteristics of eight children diagnosed with Lowe syndrome in southern China, and performs functional analysis of the novel variants. METHODS: Whole-exome sequencing was conducted on eight individuals diagnosed with Lowe syndrome from three medical institutions in southern China...
April 8, 2024: Pediatric Nephrology
https://read.qxmd.com/read/38587826/systemic-lupus-erythematosus-a-review
#32
JOURNAL ARTICLE
Caroline H Siegel, Lisa R Sammaritano
IMPORTANCE: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by inflammation and immune-mediated injury to multiple organ systems, including the mucocutaneous, musculoskeletal, hematologic, and kidney systems. Approximately 3.4 million people worldwide have received a diagnosis of SLE. OBSERVATIONS: Approximately 90% of people with SLE are female. Although there are no uniformly accepted diagnostic criteria for SLE, the 2019 European Alliance of Associations for Rheumatology (formerly the European League Against Rheumatism)/American College of Rheumatology classification criteria developed for scientific study are an estimated 96...
April 8, 2024: JAMA
https://read.qxmd.com/read/38587559/idiopathic-nephrotic-syndrome-in-syrian-children-clinicopathological-spectrum-treatment-and-outcomes
#33
JOURNAL ARTICLE
Hala Wannous
BACKGROUND: Idiopathic nephrotic syndrome (INS) is the most common glomerular disease in children. We performed this study to report histopathological findings, the correlation between clinical and histopathological features, and the response to steroids and other immunosuppressive drugs and outcomes in Syrian children with INS. METHODS: A single-center retrospective observational cohort study was conducted at Children's University Hospital in Damascus, and included all patients aged 1-14 years, admitted from January 2013 to December 2022, with INS and who underwent kidney biopsy...
April 8, 2024: Pediatric Nephrology
https://read.qxmd.com/read/38586611/immunologic-aspects-of-preeclampsia
#34
REVIEW
Henri Boulanger, Stéphane Bounan, Amel Mahdhi, Dominique Drouin, Salima Ahriz-Saksi, Fabien Guimiot, Nathalie Rouas-Freiss
Preeclampsia is a syndrome with multiple etiologies. The diagnosis can be made without proteinuria in the presence of dysfunction of at least 1 organ associated with hypertension. The common pathophysiological pathway includes endothelial cell activation, intravascular inflammation, and syncytiotrophoblast stress. There is evidence to support, among others, immunologic causes of preeclampsia. Unlike defense immunology, reproductive immunology is not based on immunologic recognition systems of self/non-self and missing-self but on immunotolerance and maternal-fetal cellular interactions...
February 2024: AJOG global reports
https://read.qxmd.com/read/38584847/a-narrative-review-on-adverse-drug-reactions-of-covid-19-treatments-on-the-kidney
#35
REVIEW
Fatemeh Jahanshahi, Seyed Behnam Jazayeri, Mohammad Mirahmadi Eraghi, Leonardo Oliveira Reis, Mahtab Hamidikia, Shayan Amiri, Seyed Mohammad Kazem Aghamir
Studies showed that the respiratory is not the only system affected by coronavirus 2, while cardiovascular, digestive, and nervous systems, as well as essential organs such as the kidneys, can be affected by this virus. In this review, we have studied the epidemiology, clinical, and laboratory findings on COVID-19 infection renal involvement, mortality, physiopathology, remaining renal sequels after recovery, underlying renal disease, and renal injury due to its treatment. Also, protective measures for kidney injury are explained in three levels...
2024: Open Medicine (Warsaw, Poland)
https://read.qxmd.com/read/38584832/cd36-mediated-podocyte-lipotoxicity-promotes-foot-process-effacement
#36
JOURNAL ARTICLE
Wei Hua, Lan Peng, Xue-Mei Chen, XuShun Jiang, JianGuo Hu, Xian-Hong Jiang, Xu Xiang, Jiangmin Wan, Yingfei Long, Jianqiong Xiong, Xueyi Ma, Xiaogang Du
BACKGROUND: Lipid metabolism disorders lead to lipotoxicity. The hyperlipidemia-induced early stage of renal injury mainly manifests as podocyte damage. CD36 mediates fatty acid uptake and the subsequent accumulation of toxic lipid metabolites, resulting in podocyte lipotoxicity. METHODS: Male Sprague-Dawley rats were divided into two groups: the normal control group and the high-fat diet group (HFD). Podocytes were cultured and treated with palmitic acid (PA) and sulfo- N -succinimidyl oleate (SSO)...
2024: Open Medicine (Warsaw, Poland)
https://read.qxmd.com/read/38584601/efficacy-and-safety-of-parp-inhibitors-combined-with-antiangiogenic-agents-in-the-maintenance-treatment-of-ovarian-cancer-a-systematic-review-and-meta-analysis-with-trial-sequential-analysis-of-randomized-controlled-trials
#37
Yan Wei, Li He, Tao Liu, Tao Guo, Cong Xie, Jigang Jia, Yonghong Lin, Jiang Liu, Jiayin Fan
Background: Poly (ADP-ribose) polymerase (PARP) inhibitor and antiangiogenic agent monotherapy have shown to be effective as maintenance treatment in patients with ovarian cancer (OC). However, there is currently a lack of evidence-based study to directly compare the effects of combination therapy with these two drugs. Therefore, this study aimed to compare the efficacy and safety of combination therapy with PARP inhibitors and antiangiogenic agents in women with OC using a meta-analysis. Methods: An exhaustive search of literature was undertaken using multiple databases, including PubMed, Web of Science, Embase, and the Cochrane Library to identify pertinent randomized controlled trials (RCTs) published up until 17 December 2023...
2024: Frontiers in Pharmacology
https://read.qxmd.com/read/38584145/clinicopathological-characteristics-and-gene-mutations-in-11-patients-with-lipoprotein-glomerulopathy
#38
JOURNAL ARTICLE
Yan Qin, Xiao-Jing Sun, Yi-Fang Hu, Meng Jing, Xiao-Juan Yu, Ming-Hui Zhao, Ying Tan
OBJECTIVE: Lipoprotein glomerulopathy (LPG) is a rare disorder characterized by the development of glomerular lipoprotein thrombosis. LPG exhibits familial aggregation, with mutations in the apolipoprotein E ( APOE ) gene identified as the leading cause of this disease. This study aimed to investigate APOE gene mutations and the clinicopathological features in eleven LPG patients. METHODS: Clinicopathological and follow-up data were obtained by extracting DNA, followed by APOE coding region sequencing analysis...
December 2024: Renal Failure
https://read.qxmd.com/read/38581622/cigarette-smoking-and-progression-of-kidney-dysfunction-a-longitudinal-cohort-study
#39
JOURNAL ARTICLE
Ayako Matsumoto, Yasuyuki Nagasawa, Ryouhei Yamamoto, Maki Shinzawa, Hiromitsu Yamazaki, Kensaku Shojima, Ken Shinmura, Yoshitaka Isaka, Kunitoshi Iseki, Kunihiro Yamagata, Ichiei Narita, Tsuneo Konta, Masahide Kondo, Kazuhiko Tsuruya, Masato Kasahara, Yugo Shibagaki, Shouichi Fujimoto, Koichi Asahi, Tsuyoshi Watanabe, Toshiki Moriyama
INTRODUCTION: Cigarette smoking is one of the most important life-modifiable risk factors for CVD events. The effect on CKD progression caused by smoking remained uncertain, while the effect on CVD had been established. METHOD: The study population included participants from the specific health check and specific health guidance, an annual health check-up for all inhabitants of Japan who were aged between 40 and 74 years. 149,260 subjects (male, 37.1%; female, 62...
April 6, 2024: Clinical and Experimental Nephrology
https://read.qxmd.com/read/38580974/anuria-after-kidney-transplantation-diagnosed-as-early-recurrence-of-focal-segmental-glomerulosclerosis-combined-with-acute-calcineurin-inhibitor-nephrotoxicity-a-case-report-and-literature-review
#40
REVIEW
Yoon-Ju Kim, Seong-Wook Lee, Mee-Seon Kim, Yong-Jin Kim, Ji-Young Choi, Jang-Hee Cho, Chan-Duck Kim, Yong-Lim Kim, Woo-Sung Yun, Seung Huh, Jeong-Hoon Lim, Sun-Hee Park
BACKGROUND: Primary focal segmental glomerulosclerosis (FSGS) is a glomerular disease that sometimes recurs in patients after kidney transplantation (KT) and increases the risk of graft loss. Proteinuria is a common early sign of recurrent FSGS, but an abrupt decrease in urine volume is rare. Herein, we report a patient with early recurrence of FSGS with anuria following KT. CASE PRESENTATION: A 55-year-old man with end-stage kidney disease caused by primary FSGS experienced anuria on postoperative day 2 following deceased donor KT...
April 5, 2024: BMC Nephrology
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