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: 2110

Blood Group ”a“ Was Increased in FMF Patients and Blood Group ”0“ May be Associated with Colchicine Resistance

Abdulsamet Erden1, Ezgi Deniz Batu2, Berkan Armagan3, Hafize Emine Sonmez4, Alper Sari3, Selcan Demir4, Emre Bilgin5, Esra Fırat5, Levent Kilic1, Yelda Bilginer6, Omer Karadag1, Umut Kalyoncu1 and Sedat Kiraz1, 1Department of Internal Medicine, Divison of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey, 2Department of Pediatrics, Divison of Rheumatology, Hacettepe University Faculty of Medicine, ANKARA, Turkey, 3Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey, 4Department of Pediatrics, Divison of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey, 5Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Turkey, 6Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, ANKARA, Turkey

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Autoinflammation and familial Mediterranean fever

  • 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: Miscellaneous Rheumatic and Inflammatory Diseases Poster II

Session Type: ACR Poster Session C

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

Background/Purpose: Colchicine is the main therapy for familial Mediterranean fever (FMF). However, about 5-10% of FMF patients are colchicine-resistant (1). The reason for colchicine resistance in FMF patients remains obscure. ABO genes are distributed differently among socioeconomic groups, and socioeconomic status is one of the risk factors for disease severity in FMF. To date, no report has evaluated this relation. Our aim was to investigate the association between blood groups and colchicine resistance in FMF patients.

Methods: This is a single-center, cross-sectional study. Between January and December 2016 385 FMF patients were assessed by the Adult and Pediatric Rheumatology outpatient clinics and 297 patients had blood groups (ABO and Rh) results. The blood groups in 1000 volunteer donors who admitted to the Turkish Red Crescent Blood Service in Ankara in 2015 were enrolled as healthy control group. Demographic and clinical data collected for each patient. Response to colchicine was evaluated by two experts (YB and UK). The patients were grouped into two groups: colchicine-responsive patients (Group CR) and colchicine-unresponsive patients (Group CUR).

Results: 297 patients were included in the study. As expected, the acute phase reactants were higher and arthralgia/arthritis, pleuritic chest pain, and erysipelas-like erythema were more frequent in group CUR (p<0.05). FMF patients had frequently blood group “A” than healthy controls (152/297 (51.2%) vs 420/1000 (42.0%), p=0.006). Patients with blood group “A” had 1.5 folds higher FMF compared to “non-A” blood group [OR 1.50 (95% CI 1.11-1.87)], particularly having “A” Rh (+) blood group [OR 1.47 (95% CI 1.13-1.91)]. Furthermore, patients with blood group “A” had a better response to colchicine treatment than “non-A” blood group OR 2.21 (95% CI 1.15-4.27). On the contrary, patients with blood group “0” had prominently associated with unresponsive to colchicine (Table 1).

Table 1. Comparison of blood groups between colchicine unresponsive and responsive familial Mediterranean fever (FMF)a patients

ABO / Rh blood group

Colchicine unresponsive FMFa patients (n=46)

Colchicine responsive FMFa patients (n=251)

Odds ratio

(95% CI)

P value

O

21 (45.7)

71 (28.3)

2.12 (1.12-4.04)

0. 019

Non- O

25 (54.3)

180 (71.7)

O Rh (-)

6 (13.0)

7 (2.8)

5.31 (1.69-16.62)

0.002

Non- O Rh(-)

40 (87.0)

244 (97.2)

Conclusion: It is well known that blood group A is associated with some of the Cancer such as stomach (2). It may also be related to inflammatory diseases (3). Our results may support associations of blood groups and inflammatory diseases. We demonstrated the blood subgroups and colchicine responses, as well. ABO blood group phenogroups may be used in combination with other risk factors to identify FMF patients at high risk for colchicine resistance.

References

  1. Gul A. Isr Med Assoc J 2014;16(5):281-284
  2. Wang Z. Int J Mol Sci 2012;13(10):13308-13321
  3. Melzer D. PLoS Genet 2008;4(5):e1000072

Disclosure: A. Erden, None; E. D. Batu, None; B. Armagan, None; H. E. Sonmez, None; A. Sari, None; S. Demir, None; E. Bilgin, None; E. Fırat, None; L. Kilic, None; Y. Bilginer, None; O. Karadag, None; U. Kalyoncu, None; S. Kiraz, None.

To cite this abstract in AMA style:

Erden A, Batu ED, Armagan B, Sonmez HE, Sari A, Demir S, Bilgin E, Fırat E, Kilic L, Bilginer Y, Karadag O, Kalyoncu U, Kiraz S. Blood Group ”a“ Was Increased in FMF Patients and Blood Group ”0“ May be Associated with Colchicine Resistance [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/blood-group-a-was-increased-in-fmf-patients-and-blood-group-0-may-be-associated-with-colchicine-resistance/. 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/blood-group-a-was-increased-in-fmf-patients-and-blood-group-0-may-be-associated-with-colchicine-resistance/

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