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: 2626

Proton Pump Inhibitor Induced Subacute Cutaneous Lupus Erythematosus: Clinical Characteristics and Outcomes

Yih Jia Poh1, Shirish Sangle1, Eleanor Higgins1, Emma Benton1, David McGibbon1 and David D'Cruz2, 1Louise Coote Lupus Unit, Guy's and St Thomas' Hospital, London, United Kingdom, 2Louise Coote Lupus Unit, Guy's and St. Thomas' Hospital, London, United Kingdom

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Cutaneous lupus erythematosus

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, November 7, 2017

Title: Systemic Lupus Erythematosus – Clinical Aspects and Treatment Poster III: Therapeutics and Clinical Trial Design

Session Type: ACR Poster Session C

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

Background/Purpose: Drug induced subacute cutaneous lupus erythematosus has rarely been described. There is a growing literature reporting the association between proton pump inhibitor use and subacute cutaneous lupus erythematosus (SCLE). We aim to describe the clinical characteristics of a cohort of patients with proton pump inhibitor induced subacute cutaneous lupus erythematosus, their clinical course and treatment options.

Methods: We retrospectively reviewed twelve patients with proton pump inhibitor induced subacute cutaneous lupus erythematosus at the Louise Coote Lupus Unit. Clinical details recorded included presence of underlying systemic lupus erythematosus (SLE) and SCLE, extent of cutaneous involvement, time to presentation, type of proton pump inhibitor and dosage, histological characteristics, immunological characteristics, treatment and time to resolution.

Results: There were 12 patients of whom 10 were female (83%). Eleven patients were Caucasians (92%). The median age at diagnosis was 61 years (range 37-71). Nine patients (75%) had underlying SLE. In this subgroup, only one patient had SCLE as part of their initial SLE presentation. Patients with coexisting SLE were younger with a median age of 53 years compared to patients without coexisting SLE. There were 8 patients with omeprazole, 3 patients with lansoprazole and 1 patient with pantoprazole induced SCLE.

All patients developed typical SCLE lesions clinically. The extent of SCLE was widespread involving the sun- exposed areas of the trunk, upper extremities and the lower limbs in 50% of the patients. Eleven (92%) demonstrated antinuclear antibody positivity and 9 patients (75%) anti-Ro (SS-A) antibody positivity. Seven patients underwent a skin biopsy and 6 patients had histological results in keeping with SCLE. The median time to presentation was 12 months (range 3 weeks -10 years) and the median resolution period was 19 days (range 3 days- 2 months). Proton pump inhibitors were stopped in all patients. Five patients (42%) received concurrent oral corticosteroids and 3 patients (25%) were newly initiated on hydroxychloroquine. Two patients received adjunctive topical therapy including topical steroids alone or in combination with topical tacrolimus. Four patients were re-exposed to proton pump inhibitors and 3 experienced a similar SCLE flare, which resolved following cessation of the proton pump inhibitor. (Table 1)

Conclusion: Proton pump inhibitor induced subacute cutaneous lupus may be commonly associated with anti-Ro (SS-A) antibody and this is likely a class effect with all proton pump inhibitors. In July 2015, the European Medicines Agency issued a warning that SCLE is likely to be a class effect for proton pump inhibitors. We recommend judicious use of proton pump inhibitors particularly in SLE patients with anti-Ro (SS-A) antibody positivity.


Patient, sex/age (years)

Presence of underlying Systemic Lupus Erythematosus

Antibody Profile (Extractable Nuclear Antigen, ENA)

Proton pump inhibitor /dose (mg)

Extent of SCLE skin lesion

Incubation period

Treatment

Resolution period

1; F, 53

Yes

Anti Ro (SS-A) and anti La (SS-B)

Lansoprazole, 30

Arms, anterior and posterior chest and legs

12 months

Cessation of lansoprazole, oral prednisone 7.5 mg, topical steroid (clobetasol)

3-7 days

2; F, 63

Yes

Anti Ro (SS-A) and anti La (SS-B)

Omeprazole, 20

Face, arms, torso and legs

No data

Cessation of omeprazole, hydroxychloroquine, oral prednisone

2 months

3; F, 60

No

Negative

Omeprazole, 20

Chest, upper back, abdomen and legs

3 weeks

Cessation of omeprazole

7 days

4; F, 71

Yes

Anti Ro (SS-A) and anti La (SS-B)

Omeprazole, 20

No data available

No data

Cessation of omeprazole

No data

5; F, 48

Yes

Anti Ro (SS-A)

Omeprazole, 20

Upper torso, arms and legs

2-3 months

Cessation of omeprazole, oral prednisone 20 mg (background mycophenolate mofetil 1.5 gram for SLE)

2-3 weeks

6; F, 37

Yes

Anti Ro (SS-A) and anti La (SS-B)

Pantoprazole, 40

Upper chest and back

No data

Cessation of pantoprazole (background mycophenolate mofetil and hydroxychloroquine)

No data

7; F, 65

Yes

Anti-Sm and anti-RNP

Omeprazole, 20

Face and neck

24 months

Cessation of omeprazole, hydroxychloroquine (background methotrexate for SLE)

2 months

8; M, 67

Yes

Anti Ro (SS-A) and anti La (SS-B)

Lansoprazole, 30

Face, torso, arms and legs

12 months

Cessation of lansoprazole, oral prednisone 20 mg

2 months

9; F, 45

Yes

Anti-Sm and anti-RNP

Omeprazole, 20

Neck, arms, hands and torso

3-5 weeks

Cessation of omeprazole, oral prednisone 20 mg, topical tacrolimus, topical steroid  (background hydroxychloroquine and mycophenolate mofetil 2.5 gram)

No resolution, SCLE lesions waxes and wanes

10; F, 61

No

Anti-Ro 60 and Anti La (SS-B)

Omeprazole, 40

Face and torso

6 months

Cessation of omeprazole, hydroxychloroquine

2-4 weeks

11; F, 50

Yes

Anti-Ro (SS-A) and anti-La (SS-B), anti C1q

Lansoprazole, 30

Upper back (annular polycyclic)

8 years

Cessation of lansoprazole (background hydroxychloroquine)

No data

12; M; 62

Yes

Anti-Ro and Anti-Ro60

Omeprazole, 20

Neck, arms, hands and torso

10 years

Cessation of omeprazole

2 weeks

Table 1: Clinical characteristics and outcome of patients with proton pump inhibitor induced SCLE


Disclosure: Y. J. Poh, None; S. Sangle, None; E. Higgins, None; E. Benton, None; D. McGibbon, None; D. D'Cruz, None.

To cite this abstract in AMA style:

Poh YJ, Sangle S, Higgins E, Benton E, McGibbon D, D'Cruz D. Proton Pump Inhibitor Induced Subacute Cutaneous Lupus Erythematosus: Clinical Characteristics and Outcomes [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/proton-pump-inhibitor-induced-subacute-cutaneous-lupus-erythematosus-clinical-characteristics-and-outcomes/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/proton-pump-inhibitor-induced-subacute-cutaneous-lupus-erythematosus-clinical-characteristics-and-outcomes/

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