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Home / Arthritis Center

Arthritis Center

Knuckle Cracking Q & A

Knuckle Cracking Q&A from Johns Hopkins Arthritis Center

Methotrexate Beneficial in Early Undifferentiated Arthritis

Patients with early inflammatory arthritis not meeting classification criteria for rheumatoid arthritis (RA) may have treatment delayed until typical phenotypic features accumulate. Due to the concern for toxicities of DMARDs, patients are often treated with NSAIDs and simple analgesics during this period. However, delay in DMARD treatment in early RA has been shown to result in poorer outcomes, such as irreversible radiographic damage.

Hydroxychloroquine Use May Protect Against the Development of Diabetes in RA Patient

Hydroxychloroquine (Plaquenil) is a commonly used disease modifying anti-rheumatic drug (DMARD) for RA that has known beneficial effects on blood glucose and lipids. However, whether its use can prevent the onset of diabetes in RA patients prescribed it to reduce articular signs and symptoms has not been evaluated.

Do Vitamin D Levels Affect Disease Outcomes in Rheumatoid Arthritis

In addition to its role in calcium hemostasis and bone metabolism, vitamin D also appears to be an important regulator of immune function. However, its role in modulating RA disease activity has not been studied.

Prednisone, but not TNF inhibitors, is associated with an increased risk of serious infection in older RA patients

Older person with rheumatoid arthritis (RA) make up an increasing proportion of those treated with biologic disease modifying anti-rheumatic agents (DMARDs). The safety of these agents may differ for this subgroup of older RA patients, yet effects have generally not been selectively studied in this population.

No Link Between RA Therapy and Lymphoma Observed in Large Cohort of Rheumatoid Arthritis Patients

Individuals with rheumatoid arthritis (RA) are at an increased risk for lymphoma compared to the general population, with the risk increasing in proportion to cumulative exposure to systemic inflammation. Whether RA therapies, such as biologic and non-biologic DMARDs, contribute to this risk is controversial.

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