ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1586

Resistant Hypertension Is Associated with Inflammation, Renal Function, and Increased Mortality in Patients with Systemic Lupus Erythematosus

Jocelyn Gandelman1, Megan Shuey2, April Barnado3, Li Wang4, C. Michael Stein3 and Cecilia P. Chung3, 1Vanderbilt University School of Medicine, Nashville, TN, 2Department of Pharmacology, Vanderbilt University, Nashville, TN, 3Medicine, Vanderbilt University Medical Center, Nashville, TN, 4Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Cardiovascular disease, hypertension and renal disease, Lupus, SLE

  • Tweet
  • Email
  • Print
Session Information

Date: Monday, November 6, 2017

Title: Systemic Lupus Erythematosus – Clinical Aspects and Treatment Poster II: Damage and Comorbidities

Session Type: ACR Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose: Resistant hypertension (RHTN) is defined as blood pressure that remains >140/90 mm Hg despite concurrent use of three different antihypertensive drugs. RHTN has an incidence of 0.7 cases per 100 person-years among patients with hypertension and is associated with a 47% increased risk of cardiovascular events. However, there is no information about RHTN in SLE. Therefore, we estimated the incidence of RHTN in patients with SLE and compared demographic characteristics, immunologic markers, renal function, and mortality in patients who did and did not develop RHTN.

Methods: Patients with SLE were identified from the electronic health records at an academic medical center using a validated algorithm that has a positive predictive value of 94%. The diagnosis of RHTN required the use of 3 antihypertensive drugs concurrently and a mean blood pressure >140/90 mm Hg during the following six months, or the use of ≥ 4 antihypertensive drugs simultaneously. Age, sex, race, immunologic laboratory results, creatinine concentrations at the time of first visit for SLE were compared among patients who developed RHTN and those who did not. Mortality was estimated and compared among patients with and without RHTN during subsequent follow-up.

Results: Of 1,135 patients with SLE identified, 27 were excluded due to pre-existing RHTN present before the first ICD9 code for SLE. Ninety-one patients (8.9%) developed RHTN and 1,017 did not over a follow-up of 7,689 person-years, with an incidence rate of 1.2 cases/100 person-years. Age and sex distribution were similar in patients who developed RHTN and those who did not (Table 1), but patients with RHTN were more likely to be African American (p<0.001), and had lower C3 (p=0.01), higher CRP (p<0.001), higher erythrocyte sedimentation rate (p<0.001), and higher creatinine (p<0.001) at baseline (Table 1). Twenty one patients with resistant hypertension and 111 patients without resistant hypertension died. A logistic regression model indicated higher mortality associated with RHTN [odds ratio: 2.45, (95% CI 1.45-4.14), p<0.001].

Conclusion: Patients with SLE have an incidence rate of RHTN of 1.2 cases/100 person-years, which is higher than that reported in a population of patients with hypertension. RHTN is more frequent in African-American than Caucasian lupus patients and those with low C3 levels, higher inflammatory markers, and increased creatinine. RHTN is associated with increased mortality in patients with SLE.

Table: Patient Characteristics at the time of first ICD9 Code for SLE

RHTN
n=91

No RHTN
n=1017

P-value

Demographics

Age,years

Female, n (%)

Caucasian, n (%)

African American, n (%)

Race other or unknown, n (%)

42 [22-56]

82 (90.1%)

43 (47.3%)

43 (47.3%)

5 (5.5%)

39 [27-51]

914 (89.9%)

702 (69.0%)

231 (22.7%)

84 (8.3%)

0.59

0.94

<0.001

Immunologic markers

C3, mg/dl**

C4 ,mg/dl**

CRP, mg/L**

ESR, mm/hr**

96 [69-123]

19 [14-28]

10.4 [2.8-41.7]

40 [18-78]

111 [82-132]

20 [12-28]

3.5 [1.0-12.2]

25 [10-49]

0.01

0.62

<0.001

<0.001

Creatinine (mg/dl)

1.0 [0.8-1.6]

0.8 [0.7-1.0]

<0.001

*Data were analyzed using chi-squared tests for categorical variables and Wilcoxon’s rank sum test for continuous variables. P<.05 was considered significant.

** The total SLE population was n= 1108, unless otherwise noted for the following variables: C3 (n=1007), C4 (n=914), CRP (n=757), ESR (n=947), Creatinine (n=1090)


Disclosure: J. Gandelman, None; M. Shuey, None; A. Barnado, None; L. Wang, None; C. M. Stein, Lupus Research Alliance, 2; C. P. Chung, NIH/NIAMS and Rheumatology Research Foundation, 2.

To cite this abstract in AMA style:

Gandelman J, Shuey M, Barnado A, Wang L, Stein CM, Chung CP. Resistant Hypertension Is Associated with Inflammation, Renal Function, and Increased Mortality in Patients with Systemic Lupus Erythematosus [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/resistant-hypertension-is-associated-with-inflammation-renal-function-and-increased-mortality-in-patients-with-systemic-lupus-erythematosus/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/resistant-hypertension-is-associated-with-inflammation-renal-function-and-increased-mortality-in-patients-with-systemic-lupus-erythematosus/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology