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  1. Article ; Online: Oral Anticoagulation in Patients With Advanced Chronic Kidney Disease and Atrial Fibrillation: Beyond Anticoagulation.

    Dhaese, Sofie A M / De Vriese, An S

    Mayo Clinic proceedings

    2023  Volume 98, Issue 5, Page(s) 750–770

    Abstract: The optimal approach to prevent stroke and systemic embolism in patients with advanced chronic kidney disease (CKD) and atrial fibrillation remains unresolved. We conducted a narrative review to explore areas of uncertainty and opportunities for future ... ...

    Abstract The optimal approach to prevent stroke and systemic embolism in patients with advanced chronic kidney disease (CKD) and atrial fibrillation remains unresolved. We conducted a narrative review to explore areas of uncertainty and opportunities for future research. First, the relationship between atrial fibrillation and stroke is more complex in patients with advanced CKD than in the general population. The currently employed risk stratification tools do not adequately discriminate between patients deriving a net benefit and those suffering a net harm from oral anticoagulation. Anticoagulation initiation should probably be more restrictive than is currently advocated by official guidelines. Recent evidence reveals that the superior benefit-risk profile of non-vitamin K antagonist oral anticoagulants (NOACs) vs vitamin K antagonists (VKAs) observed in the general population and in moderate CKD can be extended to advanced CKD. The NOACs yield better protection against stroke, cause less major bleeding, are associated with less acute kidney injury and a slower decline of CKD, and are associated with a lower incidence of cardiovascular events than VKAs. The VKAs may be harmful in CKD patients, in particular in patients with a high bleeding risk and labile international normalized ratio. The better safety and efficacy of NOACs as opposed to VKAs may be particularly evident in advanced CKD as a result of better on-target anticoagulation with NOACs, harmful off-target vascular effects of VKAs, and beneficial off-target vascular effects of NOACs. The intrinsic vasculoprotective effects of NOACs are supported by animal experimental evidence as well as by findings of large clinical trials and may result in use of NOACs beyond their anticoagulant properties.
    MeSH term(s) Humans ; Atrial Fibrillation/complications ; Atrial Fibrillation/drug therapy ; Atrial Fibrillation/chemically induced ; Anticoagulants/adverse effects ; Administration, Oral ; Hemorrhage/chemically induced ; Hemorrhage/drug therapy ; Stroke/etiology ; Stroke/prevention & control ; Renal Insufficiency, Chronic/complications ; Renal Insufficiency, Chronic/drug therapy
    Chemical Substances Anticoagulants
    Language English
    Publishing date 2023-04-05
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2023.01.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: First-in-human feasibility study of the aXess graft (aXess-FIH): 6-Month results.

    Tozzi, Matteo / De Letter, Jan / Krievins, Dainis / Jushinskis, Janis / D'Haeninck, Annick / Rucinskas, Kestutis / Miglinas, Marius / Baltrunas, Tomas / Nauwelaers, Sigi / De Vriese, An S / Moll, Frans / Vermassen, Frank

    The journal of vascular access

    2024  , Page(s) 11297298231220967

    Abstract: Objective: The creation of an arteriovenous fistula (AVF) is considered the most effective hemodialysis (HD) vascular access. For patients who are not suitable for AVF, arteriovenous grafts (AVGs) are the best access option for chronic HD. However, ... ...

    Abstract Objective: The creation of an arteriovenous fistula (AVF) is considered the most effective hemodialysis (HD) vascular access. For patients who are not suitable for AVF, arteriovenous grafts (AVGs) are the best access option for chronic HD. However, conventional AVGs are prone to intimal hyperplasia, stenosis, thrombosis, and infection. Xeltis has developed an AVG as a potential alternative to currently available AVGs based on the concept of endogenous tissue restoration. The results of the first 6-month follow-up are presented here.
    Methods: The aXess first-in-human (FIH) study [NCT04898153] is a prospective, single-arm, multicenter feasibility study that evaluates the early safety and performance of the aXess Hemodialysis Graft. A total of 20 patients with end-stage renal disease were enrolled across six European investigational sites.
    Results: At 6-months follow-up, all grafts were patent with primary and secondary patency rates were 80% and 100%, respectively. Three patients required a re-intervention to maintain graft patency, while one re-intervention was required to restore patency. One graft thrombosis and zero infections were reported.
    Conclusion: The expected advantages of the novel aXess Hemodialysis Graft over conventional AVGs would be evaluated by the analysis on long-term safety and effectiveness during the 5-year follow-up of the currently ongoing trial.
    Language English
    Publishing date 2024-02-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2252820-9
    ISSN 1724-6032 ; 1129-7298
    ISSN (online) 1724-6032
    ISSN 1129-7298
    DOI 10.1177/11297298231220967
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  3. Article ; Online: Humoral and Cellular Immunogenicity of the BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccine in Nursing Home Residents.

    Van Praet, Jens T / Vandecasteele, Stefaan / De Roo, Anneleen / De Vriese, An S / Reynders, Marijke

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2021  Volume 73, Issue 11, Page(s) 2145–2147

    MeSH term(s) BNT162 Vaccine ; COVID-19 ; COVID-19 Vaccines ; Humans ; Nursing Homes ; RNA, Messenger ; SARS-CoV-2
    Chemical Substances COVID-19 Vaccines ; RNA, Messenger ; BNT162 Vaccine (N38TVC63NU)
    Language English
    Publishing date 2021-04-02
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciab300
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  4. Article ; Online: Dynamics of the Cellular and Humoral Immune Response After BNT162b2 Messenger Ribonucleic Acid Coronavirus Disease 2019 (COVID-19) Vaccination in COVID-19-Naive Nursing Home Residents.

    Van Praet, Jens T / Vandecasteele, Stefaan / De Roo, Anneleen / Vynck, Matthijs / De Vriese, An S / Reynders, Marijke

    The Journal of infectious diseases

    2021  Volume 224, Issue 10, Page(s) 1690–1693

    Abstract: Short-term humoral and cellular immune responses are diminished after BNT162b2 messenger ribonucleic acid coronavirus disease 2019 (COVID-19) vaccination in COVID-19-naive nursing home residents, a population particularly vulnerable to the disease. We ... ...

    Abstract Short-term humoral and cellular immune responses are diminished after BNT162b2 messenger ribonucleic acid coronavirus disease 2019 (COVID-19) vaccination in COVID-19-naive nursing home residents, a population particularly vulnerable to the disease. We found both responses to decline after 4 weeks and remain lower than those of healthcare workers after 24 weeks, with an estimated half-life of the antibody response of 47 days. At 4 weeks, older age was significantly associated with a decreased humoral response, and diabetes mellitus and active malignancy were associated with a decreased cellular response. Our results imply that COVID-19-naive nursing home residents are a target group for booster vaccination trials.
    MeSH term(s) Antibodies, Viral ; BNT162 Vaccine ; COVID-19/prevention & control ; Humans ; Immunity, Humoral ; Nursing Homes ; RNA ; Vaccination
    Chemical Substances Antibodies, Viral ; RNA (63231-63-0) ; BNT162 Vaccine (N38TVC63NU)
    Language English
    Publishing date 2021-09-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiab458
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Study protocol of a prospective single-arm multicenter clinical study to assess the safety and performance of the aXess hemodialysis graft: The pivotal study.

    De Vriese, An S / D'Haeninck, Annick / Mendes, Artur / Ministro, Augusto / Krievins, Dainis / Kingsmore, David / Mestres, Gaspar / Villanueva, Gonzalo / Rodrigues, Hugo / Turek, Jakub / Zieliński, Maciej / De Letter, Jan / Coelho, Andreia / Loureiro, Luís Alvarenga / Tozzi, Matteo / Menegolo, Mirko / Alija, Palma Fariñas / Theodoridis, Panagiotis G / Gibbs, Paul /
    Ebrahimi, Reze / Nauwelaers, Sigi / Kakkos, Stavros K / Matoussevitch, Vladimir / Moll, Frans / Gargiulo, Mauro

    The journal of vascular access

    2023  , Page(s) 11297298231174932

    Abstract: Background: Arteriovenous grafts (AVGs) are used for patients deemed unsuitable for the creation of an autogenous arteriovenous fistula (AVF) or unable to await maturation of the AVF before starting hemodialysis. However, AVGs are prone to infection and ...

    Abstract Background: Arteriovenous grafts (AVGs) are used for patients deemed unsuitable for the creation of an autogenous arteriovenous fistula (AVF) or unable to await maturation of the AVF before starting hemodialysis. However, AVGs are prone to infection and thrombosis resulting in low long-term patency rates. The novel aXess Hemodialysis Graft consists of porous polymeric biomaterial allowing the infiltration by cells and the growth of neotissue, while the graft itself is gradually absorbed, ultimately resulting in a fully functional natural blood vessel. The Pivotal Study will examine the long-term effectiveness and safety of the aXess Hemodialysis Graft.
    Methods: The Pivotal Study is a prospective, single-arm, multicenter study that will be conducted in 110 subjects with end-stage renal disease who are not deemed suitable for the creation of an autogenous vascular access. The primary efficacy endpoint will be the primary patency rate at 6 months. The primary safety endpoint will be the freedom from device-related serious adverse events at 6 months. The secondary endpoints will include the procedural success rate, time to first cannulation, patency rates, the rate of access-related interventions to maintain patency, the freedom from device-related serious adverse events and the rate of access site infections. Patients will be followed for 60 months. An exploratory Health Economic and Outcomes Research sub-study will determine potential additional benefits of the aXess graft to patients, health care institutions, and reimbursement programs.
    Discussion: The Pivotal study will examine the long-term performance and safety of the aXess Hemodialysis Graft and compare the outcome measures with historical data obtained with other graft types and autogenous AVFs. Potential advantages may include superior long-term patency rates and lower infection rates versus currently available AVGs and a shorter time to first cannulation compared to an autologous AVF. As such, the aXess Hemodialysis Graft may fulfill an unmet clinical need in the field of hemodialysis access.
    Language English
    Publishing date 2023-05-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2252820-9
    ISSN 1724-6032 ; 1129-7298
    ISSN (online) 1724-6032
    ISSN 1129-7298
    DOI 10.1177/11297298231174932
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  6. Article: Epidemiology of native kidney disease in Flanders: results from the FCGG kidney biopsy registry.

    Laurens, Wim / Deleersnijder, Dries / Dendooven, Amélie / Lerut, Evelyne / De Vriese, An S / Dejagere, Tom / Helbert, Mark / Hellemans, Rachel / Koshy, Priyanka / Maes, Bart / Pipeleers, Lissa / Van Craenenbroeck, Amaryllis H / Van Laecke, Steven / Vande Walle, Johan / Coutteneye, Marie M / De Meester, Johan / Sprangers, Ben

    Clinical kidney journal

    2022  Volume 15, Issue 7, Page(s) 1361–1372

    Abstract: Background: The Flemish Collaborative Glomerulonephritis Group (FCGG) registry is the first population-based native kidney biopsy registry in Flanders, Belgium. In this first analysis, we report on patient demographics, frequency distribution and ... ...

    Abstract Background: The Flemish Collaborative Glomerulonephritis Group (FCGG) registry is the first population-based native kidney biopsy registry in Flanders, Belgium. In this first analysis, we report on patient demographics, frequency distribution and incidence rate of biopsied kidney disease in adults in Flanders.
    Methods: From January 2017 to December 2019, a total of 2054 adult first native kidney biopsies were included. A 'double diagnostic coding' strategy was used, in which every biopsy sample received a histopathological and final clinical diagnosis. Frequency distribution and incidence rate of both diagnoses were reported and compared with other European registries.
    Results: The median age at biopsy was 61.1 years (interquartile range, 46.1-71.7); male patients were more prevalent (62.1%) and biopsy incidence rate was 129.3 per million persons per year. Immunoglobulin A nephropathy was the most frequently diagnosed kidney disease (355 biopsies, 17.3% of total) with a similar frequency as in previously published European registries. The frequency of tubulointerstitial nephritis (220 biopsies, 10.7%) and diabetic kidney disease (154 biopsies, 7.5%) was remarkably higher, which may be attributed to changes in disease incidence as well as biopsy practices. Discordances between histopathological and final clinical diagnoses were noted and indicate areas for improvement in diagnostic coding systems.
    Conclusions: The FCGG registry, with its 'double diagnostic coding' strategy, provides useful population-based epidemiological data on a large Western European population and allows subgroup selection for future research.
    Language English
    Publishing date 2022-01-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 2655800-2
    ISSN 2048-8513 ; 2048-8505
    ISSN (online) 2048-8513
    ISSN 2048-8505
    DOI 10.1093/ckj/sfac033
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  7. Article ; Online: Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach.

    De Vriese, An S / Sethi, Sanjeev / Nath, Karl A / Glassock, Richard J / Fervenza, Fernando C

    Journal of the American Society of Nephrology : JASN

    2018  Volume 29, Issue 3, Page(s) 759–774

    Abstract: FSGS describes a renal histologic lesion with diverse causes and pathogenicities that are linked by podocyte injury and depletion. Subclasses of FSGS include primary, genetic, and secondary forms, the latter comprising maladaptive, viral, and drug- ... ...

    Abstract FSGS describes a renal histologic lesion with diverse causes and pathogenicities that are linked by podocyte injury and depletion. Subclasses of FSGS include primary, genetic, and secondary forms, the latter comprising maladaptive, viral, and drug-induced FSGS. Despite sharing certain clinical and histologic features, these subclasses differ noticeably in management and prognosis. Without an accepted nongenetic biomarker that discriminates among these FSGS types, classification of patients is often challenging. This review summarizes the clinical and histologic features, including the onset and severity of proteinuria as well as the presence of nephrotic syndrome, that may aid in identifying the specific FSGS subtype. The FSGS lesion is characterized by segmental sclerosis and must be differentiated from nonspecific focal global glomerulosclerosis. No light microscopic features are pathognomonic for a particular FSGS subcategory. The characteristics of podocyte foot process effacement on electron microscopy, while helpful in discriminating between primary and maladaptive FSGS, may be of little utility in detecting genetic forms of FSGS. When FSGS cannot be classified by clinicopathologic assessment, genetic analysis should be offered. Next generation DNA sequencing enables cost-effective screening of multiple genes simultaneously, but determining the pathogenicity of a detected genetic variant may be challenging. A more systematic evaluation of patients, as suggested herein, will likely improve therapeutic outcomes and the design of future trials in FSGS.
    MeSH term(s) Diagnosis, Differential ; Genetic Testing ; Glomerulosclerosis, Focal Segmental/classification ; Glomerulosclerosis, Focal Segmental/diagnosis ; Glomerulosclerosis, Focal Segmental/genetics ; Glomerulosclerosis, Focal Segmental/pathology ; Humans ; Microscopy, Electron ; Microscopy, Fluorescence ; Nephrotic Syndrome/etiology ; Podocytes/pathology ; Proteinuria/etiology
    Language English
    Publishing date 2018-01-10
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1085942-1
    ISSN 1533-3450 ; 1046-6673
    ISSN (online) 1533-3450
    ISSN 1046-6673
    DOI 10.1681/ASN.2017090958
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  8. Article ; Online: A Target Antigen-Based Approach to the Classification of Membranous Nephropathy.

    Bobart, Shane A / Tehranian, Shahrzad / Sethi, Sanjeev / Alexander, Mariam P / Nasr, Samih H / Moura Marta, Casal / Vrana, Julie A / Said, Samar / Giesen, Callen D / Lieske, John C / Fervenza, Fernando C / De Vriese, An S

    Mayo Clinic proceedings

    2021  Volume 96, Issue 3, Page(s) 577–591

    Abstract: Objective: To describe the clinical and pathological phenotype of membranous nephropathy (MN) associated with M-type-phospholipase-A: Methods: A retrospective cohort of 270 adult patients with biopsy-proven MN diagnosed between January 2015 and April ...

    Abstract Objective: To describe the clinical and pathological phenotype of membranous nephropathy (MN) associated with M-type-phospholipase-A
    Methods: A retrospective cohort of 270 adult patients with biopsy-proven MN diagnosed between January 2015 and April 2020 was classified as PLA
    Results: Patients with PLA
    Conclusion: The widely used distinction between primary and secondary MN has limitations. We propose a refined terminology that combines the target antigen and associated disease to better classify MN and guide clinical decision making.
    MeSH term(s) Adult ; Aged ; Antigens/metabolism ; Autoantibodies/metabolism ; Cadherins/metabolism ; Female ; Glomerulonephritis, Membranous/immunology ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; N-Acetylglucosaminyltransferases/metabolism ; Neural Cell Adhesion Molecules/metabolism ; Receptors, Phospholipase A2/metabolism ; Severity of Illness Index ; Thrombospondins/metabolism
    Chemical Substances Antigens ; Autoantibodies ; Cadherins ; Neural Cell Adhesion Molecules ; PCDH7 protein, human ; PLA2R1 protein, human ; Receptors, Phospholipase A2 ; THSD7A protein, human ; Thrombospondins ; N-Acetylglucosaminyltransferases (EC 2.4.1.-) ; exostosin-1 (EC 2.4.1.224) ; exostosin-2 (EC 2.4.1.224)
    Language English
    Publishing date 2021-03-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2020.11.028
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  9. Article ; Online: Noninvasive Diagnosis of PLA2R-Associated Membranous Nephropathy: A Validation Study.

    Bobart, Shane A / Han, Heedeok / Tehranian, Shahrzad / De Vriese, An S / Roman, Juan Carlos Leon / Sethi, Sanjeev / Zand, Ladan / Andrades Gomez, Cristina / Giesen, Callen D / Soler, Maria Jose / Bomback, Andrew S / Fervenza, Fernando C

    Clinical journal of the American Society of Nephrology : CJASN

    2021  Volume 16, Issue 12, Page(s) 1833–1839

    Abstract: Background and objectives: Kidney biopsy is the current gold standard to diagnose membranous nephropathy. Approximately 70%-80% of patients with primary membranous nephropathy have circulating anti-phospholipase A2 receptor antibodies. We previously ... ...

    Abstract Background and objectives: Kidney biopsy is the current gold standard to diagnose membranous nephropathy. Approximately 70%-80% of patients with primary membranous nephropathy have circulating anti-phospholipase A2 receptor antibodies. We previously demonstrated that in proteinuric patients with preserved eGFR and absence of associated conditions (
    Design, setting, participants, & measurements: The clinical and pathologic characteristics of patients with a positive anti-phospholipase A2 receptor antibody test at the Mayo Clinic, the University Hospital Vall D'Hebron (Barcelona), and the Columbia University Medical Center (New York) were retrospectively reviewed. Biopsy findings and presence or absence of a potential associated condition were assessed.
    Results: From a total of 276 patients with positive anti-phospholipase A2 receptor serology, previously reported patients (
    Conclusions: In patients with preserved eGFR and absence of associated conditions or diabetes, a positive anti-phospholipase A2 receptor test by either ELISA >20 RU/ml or a positive immunofluorescence assay confirms the diagnosis of membranous nephropathy, precluding the requirement for a kidney biopsy.
    MeSH term(s) Humans ; Child ; Glomerulonephritis, Membranous ; Retrospective Studies ; Autoantibodies ; Enzyme-Linked Immunosorbent Assay ; Fluorescent Antibody Technique ; Receptors, Phospholipase A2
    Chemical Substances Autoantibodies ; Receptors, Phospholipase A2
    Language English
    Publishing date 2021-11-15
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2226665-3
    ISSN 1555-905X ; 1555-9041
    ISSN (online) 1555-905X
    ISSN 1555-9041
    DOI 10.2215/CJN.05480421
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  10. Article ; Online: C3 Glomerulopathy: Ten Years' Experience at Mayo Clinic.

    Ravindran, Aishwarya / Fervenza, Fernando C / Smith, Richard J H / De Vriese, An S / Sethi, Sanjeev

    Mayo Clinic proceedings

    2018  Volume 93, Issue 8, Page(s) 991–1008

    Abstract: Objective: To describe the clinicopathological features, complement abnormalities, triggers, treatment, and outcomes of C3 glomerulopathy.: Patients and methods: A total of 114 patients with C3 glomerulopathy seen at Mayo Clinic from January 1, 2007, ...

    Abstract Objective: To describe the clinicopathological features, complement abnormalities, triggers, treatment, and outcomes of C3 glomerulopathy.
    Patients and methods: A total of 114 patients with C3 glomerulopathy seen at Mayo Clinic from January 1, 2007, through December 31, 2016, were evaluated in this study.
    Results: The mean age at diagnosis for the entire cohort was 40.4±22.3 years, with a median serum creatinine level and proteinuria value of 1.6 mg/dL (range: 0.3-14.7) (to convert to mmol/L, multiply by 0.0259) and 2605 mg/24 h (range: 233-24,165), respectively. Hematuria was present in 100 patients (87.7%). The C3 and C4 levels were low in 50 of 112 (44.6%) and 13 of 110 (11.8%) patients, respectively. A history of infection, positive autoimmune findings, and monoclonal gammopathy (MIg) were present in 33 of 114 (28.9%), 28 of 114 (24.6%), and 36 of 95 (37.9%) patients, respectively. However, 28 of 43 patients 50 years or older (65.1%) had MIg. A genetic variant in complement genes, C3 nephritic factor (C3Nef), and other autoantibodies was present in 26 of 70 (37.1%), 30 of 69 (43.5%), and 9 of 67 (13.4%) patients, respectively. Membranoproliferative and mesangial proliferative glomerulonephritis were the common patterns of injury. Patients without MIg were younger (mean age, 32.3±20.6 years), with a median serum creatinine level and proteinuria value of 1.4 mg/dL (range: 0.3-7.9) and 2450 mg/24 h (range: 250-24, 165) and with low C3 and C4 levels in 38 of 77 (49.4%) and 9 of 75 (12.0%) patients, respectively. Most patients received corticosteroids and other immunosuppressive drugs. In patients without MIg, at a median follow-up of 22.3 months (range: 0.1-201.1), the median serum creatinine level and proteinuria value were 1.4 mg/dL (range: 0.3-3.7) and 825.5 mg/24 h (range: 76-22, 603), and 7 patients (9.2%) had progression to end-stage renal disease.
    Conclusion: C3 glomerulopathy is a heterogeneous disease entity with complex triggering events and abnormalities of the alternative pathway of complement. The disease tends to be progressive and exhibits a variable response to immunosuppressive therapy.
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Autoantibodies/blood ; Autoimmune Diseases/epidemiology ; Child ; Child, Preschool ; Complement C3/genetics ; Complement C3 Nephritic Factor/analysis ; Complement Factor H/genetics ; Complement System Proteins ; Creatinine/blood ; Disease Progression ; Female ; Genetic Variation ; Glomerulonephritis/blood ; Glomerulonephritis/drug therapy ; Glomerulonephritis/genetics ; Glucocorticoids/therapeutic use ; Hematuria/epidemiology ; Humans ; Immunoglobulins/blood ; Immunosuppressive Agents/therapeutic use ; Infections/epidemiology ; Kidney Failure, Chronic/epidemiology ; Male ; Middle Aged ; Minnesota/epidemiology ; Nephrotic Syndrome/epidemiology ; Paraproteinemias/epidemiology ; Proteinuria/epidemiology ; Young Adult
    Chemical Substances Autoantibodies ; C3 protein, human ; Complement C3 ; Complement C3 Nephritic Factor ; Glucocorticoids ; Immunoglobulins ; Immunosuppressive Agents ; complement 4 nephritic factor ; Complement Factor H (80295-65-4) ; Complement System Proteins (9007-36-7) ; Creatinine (AYI8EX34EU)
    Language English
    Publishing date 2018-06-05
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 124027-4
    ISSN 1942-5546 ; 0025-6196
    ISSN (online) 1942-5546
    ISSN 0025-6196
    DOI 10.1016/j.mayocp.2018.05.019
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