Literature DB >> 24890338

Defining nephrotic syndrome from an integrative genomics perspective.

Matthew G Sampson1, Jeffrey B Hodgin, Matthias Kretzler.   

Abstract

Nephrotic syndrome (NS) is a clinical condition with a high degree of morbidity and mortality, caused by failure of the glomerular filtration barrier, resulting in massive proteinuria. Our current diagnostic, prognostic and therapeutic decisions in NS are largely based upon clinical or histological patterns such as "focal segmental glomerulosclerosis" or "steroid sensitive". Yet these descriptive classifications lack the precision to explain the physiologic origins and clinical heterogeneity observed in this syndrome. A more precise definition of NS is required to identify mechanisms of disease and capture various clinical trajectories. An integrative genomics approach to NS applies bioinformatics and computational methods to comprehensive experimental, molecular and clinical data for holistic disease definition. A unique aspect is analysis of data together to discover NS-associated molecules, pathways, and networks. Integrating multidimensional datasets from the outset highlights how molecular lesions impact the entire individual. Data sets integrated range from genetic variation to gene expression, to histologic changes, to progression of chronic kidney disease (CKD). This review will introduce the tenets of integrative genomics and suggest how it can increase our understanding of NS from molecular and pathophysiological perspectives. A diverse group of genome-scale experiments are presented that have sought to define molecular signatures of NS. Finally, the Nephrotic Syndrome Study Network (NEPTUNE) will be introduced as an international, prospective cohort study of patients with NS that utilizes an integrated systems genomics approach from the outset. A major NEPTUNE goal is to achieve comprehensive disease definition from a genomics perspective and identify shared molecular drivers of disease.

Entities:  

Mesh:

Year:  2014        PMID: 24890338      PMCID: PMC4241380          DOI: 10.1007/s00467-014-2857-9

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  103 in total

Review 1.  Circulating permeability factors in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

Authors:  Ellen T McCarthy; Mukut Sharma; Virginia J Savin
Journal:  Clin J Am Soc Nephrol       Date:  2010-10-21       Impact factor: 8.237

2.  Integrative urinary peptidomics in renal transplantation identifies biomarkers for acute rejection.

Authors:  Xuefeng B Ling; Tara K Sigdel; Kenneth Lau; Lihua Ying; Irwin Lau; James Schilling; Minnie M Sarwal
Journal:  J Am Soc Nephrol       Date:  2010-02-11       Impact factor: 10.121

3.  The APOL1 genotype of African American kidney transplant recipients does not impact 5-year allograft survival.

Authors:  B T Lee; V Kumar; T A Williams; R Abdi; A Bernhardy; C Dyer; S Conte; G Genovese; M D Ross; D J Friedman; R Gaston; E Milford; M R Pollak; A Chandraker
Journal:  Am J Transplant       Date:  2012-04-04       Impact factor: 8.086

4.  APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy.

Authors:  Jeffrey B Kopp; George W Nelson; Karmini Sampath; Randall C Johnson; Giulio Genovese; Ping An; David Friedman; William Briggs; Richard Dart; Stephen Korbet; Michele H Mokrzycki; Paul L Kimmel; Sophie Limou; Tejinder S Ahuja; Jeffrey S Berns; Justyna Fryc; Eric E Simon; Michael C Smith; Howard Trachtman; Donna M Michel; Jeffrey R Schelling; David Vlahov; Martin Pollak; Cheryl A Winkler
Journal:  J Am Soc Nephrol       Date:  2011-10-13       Impact factor: 10.121

Review 5.  APOL1 and kidney disease.

Authors:  Martin R Pollak; Giulio Genovese; David J Friedman
Journal:  Curr Opin Nephrol Hypertens       Date:  2012-03       Impact factor: 2.894

Review 6.  Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients.

Authors:  Jeremy Kiffel; Yael Rahimzada; Howard Trachtman
Journal:  Adv Chronic Kidney Dis       Date:  2011-09       Impact factor: 3.620

7.  Increased serum and urinary microRNAs in children with idiopathic nephrotic syndrome.

Authors:  Yang Luo; Cheng Wang; Xi Chen; Tianying Zhong; Xiaoyi Cai; Sidi Chen; Yonghui Shi; Jing Hu; Xiaocui Guan; Zhengkun Xia; Junjun Wang; Ke Zen; Chen-Yu Zhang; Chunni Zhang
Journal:  Clin Chem       Date:  2013-01-23       Impact factor: 8.327

Review 8.  RNA-Seq: a revolutionary tool for transcriptomics.

Authors:  Zhong Wang; Mark Gerstein; Michael Snyder
Journal:  Nat Rev Genet       Date:  2009-01       Impact factor: 53.242

9.  The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children.

Authors: 
Journal:  J Pediatr       Date:  1981-04       Impact factor: 4.406

Review 10.  Genetic kidney diseases.

Authors:  Friedhelm Hildebrandt
Journal:  Lancet       Date:  2010-04-10       Impact factor: 79.321

View more
  13 in total

Review 1.  Morphology in the Digital Age: Integrating High-Resolution Description of Structural Alterations With Phenotypes and Genotypes.

Authors:  Cynthia C Nast; Kevin V Lemley; Jeffrey B Hodgin; Serena Bagnasco; Carmen Avila-Casado; Stephen M Hewitt; Laura Barisoni
Journal:  Semin Nephrol       Date:  2015-05       Impact factor: 5.299

2.  A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis.

Authors:  Haiyang Yu; Mykyta Artomov; Sebastian Brähler; M Christine Stander; Ghaidan Shamsan; Matthew G Sampson; J Michael White; Matthias Kretzler; Jeffrey H Miner; Sanjay Jain; Cheryl A Winkler; Robi D Mitra; Jeffrey B Kopp; Mark J Daly; Andrey S Shaw
Journal:  J Clin Invest       Date:  2016-02-22       Impact factor: 14.808

Review 3.  The nephrologist of tomorrow: towards a kidney-omic future.

Authors:  Mina H Hanna; Alessandra Dalla Gassa; Gert Mayer; Gianluigi Zaza; Patrick D Brophy; Loreto Gesualdo; Francesco Pesce
Journal:  Pediatr Nephrol       Date:  2016-03-09       Impact factor: 3.714

Review 4.  Treatment of nephrotic syndrome: going beyond immunosuppressive therapy.

Authors:  Jinghong Zhao; Zhihong Liu
Journal:  Pediatr Nephrol       Date:  2019-03-23       Impact factor: 3.714

5.  Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study.

Authors:  Rajiv Sinha; Subal Pradhan; Sushmita Banerjee; Afsana Jahan; Shakil Akhtar; Amitava Pahari; Sumantra Raut; Prince Parakh; Surupa Basu; Priyanka Srivastava; Snehamayee Nayak; S G Thenral; V Ramprasad; Emma Ashton; Detlef Bockenhauer; Kausik Mandal
Journal:  Pediatr Nephrol       Date:  2022-01-10       Impact factor: 3.651

6.  Molecular Characterization of Membranous Nephropathy.

Authors:  Rachel Sealfon; Laura Mariani; Carmen Avila-Casado; Viji Nair; Rajasree Menon; Julien Funk; Aaron Wong; Gabriel Lerner; Norifumi Hayashi; Olga Troyanskaya; Matthias Kretzler; Laurence H Beck
Journal:  J Am Soc Nephrol       Date:  2022-04-27       Impact factor: 14.978

Review 7.  Research Infrastructure for Collaborative Team Science: Challenges in Technology-Supported Workflows in and Across Laboratories, Institutions, and Geographies.

Authors:  Barbara Mirel; Airong Luo; Marcelline Harris
Journal:  Semin Nephrol       Date:  2015-05       Impact factor: 5.299

8.  Promises and pitfalls of whole-exome sequencing exemplified by a nephrotic syndrome family.

Authors:  Mara Sanches Guaragna; Anna Cristina Gervásio de Brito Lutaif; Marcela Lopes de Souza; Andréa Trevas Maciel-Guerra; Vera Maria Santoro Belangero; Gil Guerra-Júnior; Maricilda Palandi de Mello
Journal:  Mol Genet Genomics       Date:  2019-09-13       Impact factor: 3.291

Review 9.  Genetics of hereditary nephrotic syndrome: a clinical review.

Authors:  Tae-Sun Ha
Journal:  Korean J Pediatr       Date:  2017-03-27

10.  A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.

Authors:  Markus M Rinschen; Markus Gödel; Florian Grahammer; Stefan Zschiedrich; Martin Helmstädter; Oliver Kretz; Mostafa Zarei; Daniela A Braun; Sebastian Dittrich; Caroline Pahmeyer; Patricia Schroder; Carolin Teetzen; HeonYung Gee; Ghaleb Daouk; Martin Pohl; Elisa Kuhn; Bernhard Schermer; Victoria Küttner; Melanie Boerries; Hauke Busch; Mario Schiffer; Carsten Bergmann; Marcus Krüger; Friedhelm Hildebrandt; Joern Dengjel; Thomas Benzing; Tobias B Huber
Journal:  Cell Rep       Date:  2018-05-22       Impact factor: 9.423

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.