Rarity of anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase antibodies in statin users, including those with self‐limited musculoskeletal side effects

Objective Statins, among the most commonly prescribed medications, are associated with a wide range of musculoskeletal side effects. These include a progressive autoimmune myopathy with anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase (anti‐HMGCR) antibodies that requires immunosuppression. Howe...

Full description

Saved in:
Bibliographic Details
Published inArthritis care & research (2010) Vol. 64; no. 2; pp. 269 - 272
Main Authors Mammen, Andrew L., Pak, Katherine, Williams, Emma K., Brisson, Diane, Coresh, Joe, Selvin, Elizabeth, Gaudet, Daniel
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.02.2012
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Objective Statins, among the most commonly prescribed medications, are associated with a wide range of musculoskeletal side effects. These include a progressive autoimmune myopathy with anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase (anti‐HMGCR) antibodies that requires immunosuppression. However, it remains unknown whether these antibodies are found in statin users with and without self‐limited musculoskeletal side effects; this limits their diagnostic utility. The current work assessed the prevalence of anti‐HMGCR antibodies in these groups of statin users. Methods We determined the prevalence of anti‐HMGCR antibodies in 1,966 participants (including 763 current statin users) in a substudy of the community‐based Atherosclerosis Risk in Communities (ARIC) Study and 98 French Canadian subjects with familial hypercholesterolemia, including 51 with documented statin intolerance. Results No participant in the ARIC substudy, including those with past or current statin exposure at the time of sample collection, had anti‐HMGCR antibodies. Similarly, none of 51 patients with self‐limited statin intolerance or 47 statin‐tolerant patients receiving maximal statin therapy were anti‐HMGCR positive. Conclusion The majority of patients with and without statin exposure, including those with self‐limited statin intolerance, do not develop anti‐HMGCR antibodies. Therefore, anti‐HMGCR antibodies are highly specific for those with an autoimmune myopathy.
Bibliography:Drs. Selvin and Gaudet contributed equally to this work.
Dr. Mammen has a provisional patent on an anti–3‐ hydroxy‐3‐methylglutaryl‐coenzyme A assay; this has not been licensed.
Dr. Coresh has received consultant fees, speaking fees, and/or honoraria (less than $10,000 each) from Amgen International and Merck.
Dr. Gaudet is chair holder of the Canada Research Chair in preventive genetics and community genomics.
ISSN:2151-464X
2151-4658
DOI:10.1002/acr.20662