AI Article Synopsis

  • The study investigates the prevalence of subclinical amyloidosis in rheumatoid arthritis (RA) patients using abdominal fat aspiration biopsy (AFAB) and minor salivary gland biopsy (MSGB), finding a high prevalence rate of 21.5% with AFAB.
  • Factors linked to subclinical amyloidosis include a longer time to diagnosis, extraarticular manifestations, higher levels of proteinuria, and the absence of methotrexate therapy, but not demographics or other health metrics.
  • The authors recommend using AFAB as a screening tool for patients at risk, emphasizing the importance of monitoring subclinical amyloidosis to catch more serious symptoms early.

Article Abstract

Introduction: Secondary amyloidosis is a serious complication of rheumatoid arthritis (RA). Symptoms are late to occur, so that screening is in order, most notably in patients with long-standing RA. The objectives of our study were to determine the prevalence of subclinical amyloidosis in RA patients by abdominal fat aspiration biopsy (AFAB) and minor salivary gland biopsy (MSGB) and to identify factors associated with subclinical amyloidosis.

Methods: We prospectively studied 107 consecutive patients with RA (94 women and 13 men) recruited between March 2005 and January 2006. Clinical and laboratory findings, imaging study results, and treatment were recorded for each patient. AFAB and MSGB were performed routinely. Amyloid deposits were identified by polarized light microscopy after Congo red staining.

Results: The prevalence of subclinical amyloidosis was 21.5% by AFAB and 3.7% by MSGB. Factors associated with subclinical amyloidosis were a longer time to diagnosis (P=0.03), extraarticular manifestations (P=0.019), proteinuria >0.3 g/24 h (P=0.024), and absence of methotrexate therapy (P=0.046). Subclinical amyloidosis was not associated with age, sex, RA duration, joint deformities, DAS28 score, Health Assessment Questionnaire score, Steinbrocker radiological stage, rheumatoid factor, erythrocyte sedimentation rate, C-reactive protein, creatinine, or hemoglobin.

Conclusion: The prevalence of subclinical amyloidosis by AFAB is high (21.5%). AFAB is more sensitive than MSGB for detecting subclinical amyloidosis. A simple screening tool such as AFAB should be used, particularly in patients with risk factors. Subclinical amyloidosis requires close monitoring to ensure the early detection and treatment of symptomatic amyloidosis.

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Source
http://dx.doi.org/10.1016/j.jbspin.2008.08.009DOI Listing

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