67. Brain Th17 Cells in Mice With Depressive-Like Behavior: Towards Novel Treatment Targets

2018 ◽  
Vol 83 (9) ◽  
pp. S27-S28
Author(s):  
Eleonore Beurel
2019 ◽  
Vol 22 (1) ◽  
pp. 70-80 ◽  
Author(s):  
Thong H. Cao ◽  
Donald J.L. Jones ◽  
Adriaan A. Voors ◽  
Paulene A. Quinn ◽  
Jatinderpal K. Sandhu ◽  
...  

2020 ◽  
Vol 288 (5) ◽  
pp. 491-506 ◽  
Author(s):  
A. Pol ◽  
M. F. Hoes ◽  
R. A. Boer ◽  
P. Meer

2020 ◽  
Vol 35 (Supplement_3) ◽  
Author(s):  
Eunjeong Kang ◽  
Yaerim Kim ◽  
Yong Chul Kim ◽  
Soojin Lee ◽  
Seungyeup Han ◽  
...  

Abstract Background and Aims Glomerular diseases, a set of debilitating and complex disease entities, are related to mortality and morbidity. To gain insight into pathophysiology and novel treatment targets of glomerular disease, various types of biospecimens linked to deep clinical phenotyping including clinical information, digital pathology, and well-defined outcomes are required. We provide the rationale and design of the KOrea Renal biobank NEtwoRk System TOward Next-generation analysis (KORNERSTONE). Method The KORNERSTONE, which has been initiated by Korea Centres for Disease Control and Prevention, is designed as a multi-centre, prospective cohort study and biobank for glomerular diseases. Clinical data, questionnaires will be collected at the time of kidney biopsy and subsequently every one year after kidney biopsy. All of the clinical data will be extracted from the electrical health record and automatically uploaded to the web-based database. High-quality digital pathologies are obtained and connected in the database. Various types of biospecimens are collected at baseline and during follow-up: serum, urine, buffy coat, stool, glomerular complementary DNA (cDNA), tubulointerstitial cDNA. All data and biospecimens are processed and stored in a standardised manner. The primary outcomes are mortality and end-stage renal disease. The secondary outcomes will be deterioration renal function, remission of proteinuria, cardiovascular events and quality of life. Disussion Ethical approval has been obtained from the institutional review board of each participating centre and ethics oversight committee. The KORNERSTONE is designed to deliver pioneer insights into glomerular diseases. The study design allows comprehensive, integrated and high-quality data collection on baseline laboratory findings, clinical outcomes including administrative data and digital pathologic images. This may provide various biospecimens and information to many researchers, establish the rationale for future more individualised treatment strategies for glomerular diseases. Conclusion In conclusion, we describe the objectives and clinical protocol for the KORNERSTONE. As the first large-scale glomerulonephropathy cohort study with the integration of clinical data, biospecimens and digital pathologic images in Korea, the KORNERSTONE will help to clarify the natural course, complication profiles, and novel treatment targets of the Asian population with glomerular disease.


Author(s):  
Błażej Misiak ◽  
Jan Aleksander Beszłej ◽  
Kamila Kotowicz ◽  
Monika Szewczuk-Bogusławska ◽  
Jerzy Samochowiec ◽  
...  

2011 ◽  
Vol 9 (1) ◽  
pp. 65-72 ◽  
Author(s):  
Brian P. Walcott ◽  
Kristopher T. Kahle ◽  
J. Marc Simard

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
David R. Goldsmith ◽  
Nicholas Massa ◽  
Brian J. Miller ◽  
Andrew H. Miller ◽  
Erica Duncan

AbstractFinding biological predictors and novel mechanisms underlying negative symptoms of schizophrenia is of significant importance given the lack of effective treatments. Increasing data support a role for metabolic dysfunction and inflammation in reward processing deficits in psychiatric illness. Herein, we found an interaction between lipids and inflammation as a predictor of worse negative symptom severity in individuals with schizophrenia. Future studies may seek to further elucidate this relationship and thereby reveal novel treatment targets for negative symptoms.


2018 ◽  
Vol 189 ◽  
pp. 184-198 ◽  
Author(s):  
Emily G. Severance ◽  
Faith B. Dickerson ◽  
Robert H. Yolken

Neuron ◽  
2014 ◽  
Vol 84 (3) ◽  
pp. 537-541 ◽  
Author(s):  
Christian R. Schubert ◽  
Hualin S. Xi ◽  
Jens R. Wendland ◽  
Patricio O’Donnell

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