Literature DB >> 22271756

Glucocorticoid use and abuse in SLE.

Guillermo Ruiz-Irastorza1, Alvaro Danza, Munther Khamashta.   

Abstract

Glucocorticoids (GCs) are potent anti-inflammatory and immunosuppressive agents. They act by two different mechanisms: the genomic and the non-genomic pathways. The genomic pathway is considered responsible for many adverse effects of GCs, most of them are time and dose dependent. Observational studies support a relationship between GCs and damage in SLE. GCs have been associated with the development of osteoporosis, osteonecrosis, cataracts, hyperglycaemia, coronary heart disease and cognitive impairment, among others. Although no clinical trial has compared high vs low doses of GCs, some studies have shown the efficacy of medium doses in severe forms of SLE. The dose below which treatment can be considered safe has not been defined, but daily doses <7.5 mg of prednisone seem to minimize adverse effects. Combination therapy with HCQ and the judicious use of immunosuppressive drugs help to keep prednisone therapy within those limits.

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Year:  2012        PMID: 22271756     DOI: 10.1093/rheumatology/ker410

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  54 in total

1.  Receptor/gene/protein-mediated signaling connects methylprednisolone exposure to metabolic and immune-related pharmacodynamic actions in liver.

Authors:  Vivaswath S Ayyar; Siddharth Sukumaran; Debra C DuBois; Richard R Almon; Jun Qu; William J Jusko
Journal:  J Pharmacokinet Pharmacodyn       Date:  2018-04-27       Impact factor: 2.745

2.  Healthcare resource utilization and costs associated with long-term corticosteroid exposure in patients with systemic lupus erythematosus.

Authors:  S Kabadi; J Yeaw; A K Bacani; E Tafesse; K Bos; S Karkare; M DeKoven; E R Vina
Journal:  Lupus       Date:  2018-08-01       Impact factor: 2.911

3.  The first year results of mizoribine/tacrolimus-based multitarget treatment for consecutive patients with lupus nephritis.

Authors:  Hidetoshi Kagawa; Tsutomu Hiromasa; Ryutaro Yamanaka; Reika Hayashi; Yoko Tsunashima; Tatsuyuki Inoue; Ken-Ei Sada
Journal:  Clin Exp Nephrol       Date:  2018-06-09       Impact factor: 2.801

4.  Blunting Autoantigen-induced FOXO3a Protein Phosphorylation and Degradation Is a Novel Pathway of Glucocorticoids for the Treatment of Systemic Lupus Erythematosus.

Authors:  Mudan Lu; Wei Xu; Bo Gao; Sidong Xiong
Journal:  J Biol Chem       Date:  2016-08-01       Impact factor: 5.157

5.  Latest advances in connective tissue disorders.

Authors:  Vijay Rao; Simon Bowman
Journal:  Ther Adv Musculoskelet Dis       Date:  2013-08       Impact factor: 5.346

6.  Comparison of systemic lupus erythematosus (SLE) patients managed early after diagnosis in specialty versus community care clinics.

Authors:  Roaa Aljohani; Dafna D Gladman; Jiandong Su; Murray B Urowitz
Journal:  Clin Rheumatol       Date:  2017-06-06       Impact factor: 2.980

Review 7.  Research and therapeutics-traditional and emerging therapies in systemic lupus erythematosus.

Authors:  Laurie S Davis; Andreas M Reimold
Journal:  Rheumatology (Oxford)       Date:  2017-04-01       Impact factor: 7.580

Review 8.  Systemic lupus erythematosus: a therapeutic challenge for the XXI century.

Authors:  Manuel F Ugarte-Gil; Graciela S Alarcón
Journal:  Clin Rheumatol       Date:  2014-02-28       Impact factor: 2.980

Review 9.  Pharmacological Management of Childhood-Onset Systemic Lupus Erythematosus.

Authors:  Colin Thorbinson; Louise Oni; Eve Smith; Angela Midgley; Michael W Beresford
Journal:  Paediatr Drugs       Date:  2016-06       Impact factor: 3.022

Review 10.  Insights into the epidemiology and management of lupus nephritis from the US rheumatologist's perspective.

Authors:  Paul J Hoover; Karen H Costenbader
Journal:  Kidney Int       Date:  2016-06-22       Impact factor: 10.612

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