TY - JOUR
T1 - Impact of glucocorticoids on the incidence of lupus-related major organ damage
T2 - A systematic literature review and meta-regression analysis of longitudinal observational studies
AU - Ugarte-Gil, Manuel Francisco
AU - Mak, Anselm
AU - Leong, Joanna
AU - Dharmadhikari, Bhushan
AU - Kow, Nien Yee
AU - Reátegui-Sokolova, Cristina
AU - Elera-Fitzcarrald, Claudia
AU - Aranow, Cinthia
AU - Arnaud, Laurent
AU - Askanase, Anca D.
AU - Bae, Sang Cheol
AU - Bernatsky, Sasha
AU - Bruce, Ian N.
AU - Buyon, Jill
AU - Costedoat-Chalumeau, Nathalie
AU - Dooley, Mary Ann
AU - Fortin, Paul R.
AU - Ginzler, Ellen M.
AU - Gladman, Dafna D.
AU - Hanly, John
AU - Inanc, Murat
AU - Isenberg, David
AU - Jacobsen, Soren
AU - James, Judith A.
AU - Jönsen, Andreas
AU - Kalunian, Kenneth
AU - Kamen, Diane L.
AU - Lim, Sung Sam
AU - Morand, Eric
AU - Mosca, Marta
AU - Peschken, Christine
AU - Pons-Estel, Bernardo A.
AU - Rahman, Anisur
AU - Ramsey-Goldman, Rosalind
AU - Reynolds, John
AU - Romero-Diaz, Juanita
AU - Ruiz-Irastorza, Guillermo
AU - Sánchez-Guerrero, Jorge
AU - Svenungsson, Elisabet
AU - Urowitz, Murray
AU - Vinet, Evelyne
AU - Van Vollenhoven, Ronald F.
AU - Voskuyl, Alexandre
AU - Wallace, Daniel J.
AU - Petri, Michelle A.
AU - Manzi, Susan
AU - Clarke, Ann Elaine
AU - Cheung, Mike
AU - Farewell, Vernon
AU - Alarcon, Graciela S.
N1 - Publisher Copyright:
© Authors 2021
PY - 2021/12/20
Y1 - 2021/12/20
N2 - Objective In systemic lupus erythematosus (SLE), disease activity and glucocorticoid (GC) exposure are known to contribute to irreversible organ damage. We aimed to examine the association between GC exposure and organ damage occurrence. Methods We conducted a literature search (PubMed (Medline), Embase and Cochrane January 1966-October 2021). We identified original longitudinal observational studies reporting GC exposure as the proportion of users and/or GC use with dose information as well as the occurrence of new major organ damage as defined in the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index. Meta-regression analyses were performed. Reviews, case-reports and studies with <5 years of follow-up, <50 patients, different outcomes and special populations were excluded. Results We selected 49 articles including 16 224 patients, 14 755 (90.9%) female with a mean age and disease duration of 35.1 years and of 37.1 months. The mean follow-up time was 104.9 months. For individual damage items, the average daily GC dose was associated with the occurrence of overall cardiovascular events and with osteoporosis with fractures. A higher average cumulative dose adjusted (or not)/number of follow-up years and a higher proportion of patients on GC were associated with the occurrence of osteonecrosis. Conclusions We confirm associations of GC use with three specific damage items. In treating patients with SLE, our aim should be to maximise the efficacy of GC and to minimise their harms.
AB - Objective In systemic lupus erythematosus (SLE), disease activity and glucocorticoid (GC) exposure are known to contribute to irreversible organ damage. We aimed to examine the association between GC exposure and organ damage occurrence. Methods We conducted a literature search (PubMed (Medline), Embase and Cochrane January 1966-October 2021). We identified original longitudinal observational studies reporting GC exposure as the proportion of users and/or GC use with dose information as well as the occurrence of new major organ damage as defined in the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index. Meta-regression analyses were performed. Reviews, case-reports and studies with <5 years of follow-up, <50 patients, different outcomes and special populations were excluded. Results We selected 49 articles including 16 224 patients, 14 755 (90.9%) female with a mean age and disease duration of 35.1 years and of 37.1 months. The mean follow-up time was 104.9 months. For individual damage items, the average daily GC dose was associated with the occurrence of overall cardiovascular events and with osteoporosis with fractures. A higher average cumulative dose adjusted (or not)/number of follow-up years and a higher proportion of patients on GC were associated with the occurrence of osteonecrosis. Conclusions We confirm associations of GC use with three specific damage items. In treating patients with SLE, our aim should be to maximise the efficacy of GC and to minimise their harms.
KW - glucocorticoids
KW - health care
KW - lupus erythematosus
KW - outcome assessment
KW - systemic
UR - http://www.scopus.com/inward/record.url?scp=85122251038&partnerID=8YFLogxK
U2 - 10.1136/lupus-2021-000590
DO - 10.1136/lupus-2021-000590
M3 - Artículo de revisión
AN - SCOPUS:85122251038
SN - 2053-8790
VL - 8
JO - Lupus Science and Medicine
JF - Lupus Science and Medicine
IS - 1
M1 - e000590
ER -