Increased Incidence of Resistant Hypertension in Patients With Systemic Lupus Erythematosus: A Retrospective Cohort Study.


Journal

Arthritis care & research
ISSN: 2151-4658
Titre abrégé: Arthritis Care Res (Hoboken)
Pays: United States
ID NLM: 101518086

Informations de publication

Date de publication:
04 2020
Historique:
received: 06 06 2018
accepted: 05 03 2019
pubmed: 16 3 2019
medline: 21 7 2020
entrez: 16 3 2019
Statut: ppublish

Résumé

To compare the risk of resistant hypertension (RHTN) in patients with systemic lupus erythematosus (SLE) and in controls without SLE, and to define factors associated with RHTN in patients with SLE. We studied 1,044 patients with SLE and 5,241 control subjects using de-identified electronic health records from a tertiary care center. SLE was defined as ≥4 International Classification of Diseases, Ninth Revision codes for SLE and antinuclear antibody titer ≥1:160. RHTN was defined as uncontrolled blood pressure on 3 antihypertensive medications or requiring 4 or more antihypertensives to attain control. First, we compared the risk of RHTN between groups. Second, we examined the association between RHTN and all-cause mortality in patients with SLE. RHTN was nearly twice as prevalent in patients with SLE compared to control subjects (10.2% and 5.3%, respectively), with an incidence rate of 10.2 versus 6.1 cases per 1,000 person-years of observation (hazard ratio [HR] 1.72 [95% confidence interval 1.28-2.30]; P < 0.001, adjusted for age, sex, race, baseline end-stage renal disease [ESRD], creatinine, and calendar year). In patients with SLE, we found associations between RHTN and black race, lower renal function, hypercholesterolemia, and increased inflammatory markers. RHTN was associated with a significantly higher mortality risk (HR 2.91, P = 0.0005) after adjustment for age, sex, race, calendar year, creatinine, baseline ESRD, and number of visits. Patients with SLE have a higher risk of RHTN compared to frequency-matched controls, independent of multiple covariates. RHTN is an important comorbidity for clinicians to recognize in SLE, because it is associated with a higher risk of mortality.

Identifiants

pubmed: 30875459
doi: 10.1002/acr.23880
pmc: PMC6745299
mid: NIHMS1016775
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

534-543

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR000445
Pays : United States
Organisme : NIDDK NIH HHS
ID : F31 DK108444
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007569
Pays : United States
Organisme : NIAMS NIH HHS
ID : K23 AR064768
Pays : United States
Organisme : NIAMS NIH HHS
ID : K08 AR072757
Pays : United States
Organisme : NICHD NIH HHS
ID : K12 HD043483
Pays : United States

Informations de copyright

© 2019, American College of Rheumatology.

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Auteurs

Jocelyn S Gandelman (JS)

Vanderbilt University School of Medicine, Nashville, Tennessee.

Omair A Khan (OA)

Vanderbilt University Medical Center, Nashville, Tennessee.

Megan M Shuey (MM)

Vanderbilt University, Nashville, Tennessee.

Jacquelyn E Neal (JE)

Vanderbilt University School of Medicine, Nashville, Tennessee.

Elizabeth McNeer (E)

Vanderbilt University Medical Center, Nashville, Tennessee.

Alyson Dickson (A)

Vanderbilt University Medical Center, Nashville, Tennessee.

April Barnado (A)

Vanderbilt University Medical Center, Nashville, Tennessee.

Li Wang (L)

Vanderbilt University Medical Center, Nashville, Tennessee.

Prathima Anandi (P)

Vanderbilt University Medical Center, Nashville, Tennessee.

William D Dupont (WD)

Vanderbilt University School of Medicine, Nashville, Tennessee.

C Michael Stein (CM)

Vanderbilt University Medical Center, Nashville, Tennessee.

Cecilia P Chung (CP)

Vanderbilt University Medical Center, Nashville, Tennessee.

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