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Frequency of methotrexate intolerance in rheumatoid arthritis patients using methotrexate intolerance severity score
Nibah Fatimah1,2, Babur Salim3, Amjad Nasim3
1Fauji Foundation Hospital, Jhelum road, Rawalpindi, 46000, Pakistan. nibahfatimah@gmail.com.
Abstract:
The objective of the study was to determine the frequency of methotrexate intolerance in rheumatoid arthritis (RA) patients by applying the methotrexate intolerance severity score (MISS) questionnaire and to see the effect of dose and concomitant use of other disease-modifying antirheumatic drugs (DMARDS) on methotrexate (MTX) intolerance. For the descriptive study, non-probability sampling was carried out in the Female Rheumatology Department of Fauji Foundation Hospital (FFH), Rawalpindi, Pakistan. One hundred and fifty diagnosed cases of RA using oral MTX were selected. The MISS questionnaire embodies five elements: abdominal pain, nausea, vomiting, fatigue and behavioural symptoms. The amplitude of each element was ranked from 0 to 3 being no complaint (0 points), mild (1 point), moderate (2 points) and severe (3 points). A cut-off score of 6 and above ascertained intolerance by the physicians. A total of 33.3 % of the subjects exhibited MTX intolerance according to the MISS questionnaire. Out of which, the most recurring symptom of all was behavioural with a value of 44 % whereas vomiting was least noticeable with a figure of 11 %. About 6.6 % of the women with intolerance were consuming DMARDs in conjunction with MTX. Those using the highest weekly dose of MTX (20 mg) had supreme intolerance with prevalence in 46.2 % of the patients. The frequency of intolerance decreased with a decrease in weekly dose to a minimum of 20 % with 7.5 mg of MTX. MTX intolerance has moderate prevalence in RA patients and if left undetected, the compliance to use of MTX as a first-line therapy will decrease. Methotrexate intolerance is directly proportional to the dose of MTX taken. Also, there is no upstroke seen in intolerance with the use of other disease-modifying agents.
Insights
Methotrexate intolerance affects 33.3% of rheumatoid arthritis patients, with behavioral symptoms being most common. Higher methotrexate doses increase intolerance risk, impacting treatment adherence.
Area of Science:
- Rheumatology
- Clinical Pharmacology
Background:
- Rheumatoid arthritis (RA) management often involves methotrexate (MTX), a cornerstone disease-modifying antirheumatic drug (DMARD).
- Methotrexate intolerance (MTX-I) can significantly impact patient adherence and treatment outcomes.
- Understanding the prevalence and contributing factors of MTX-I is crucial for optimizing RA therapy.
Purpose of the Study:
- To determine the frequency of MTX intolerance in RA patients using the Methotrexate Intolerance Severity Score (MISS) questionnaire.
- To investigate the influence of MTX dosage and concurrent use of other DMARDs on MTX intolerance.
Main Methods:
- A descriptive study was conducted with 150 female RA patients using oral MTX.
- The MISS questionnaire assessed five symptoms: abdominal pain, nausea, vomiting, fatigue, and behavioral changes, with a severity scale.
- Physicians diagnosed MTX intolerance with a MISS score of 6 or higher.
Main Results:
- A prevalence of 33.3% for MTX intolerance was observed in the study population.
- Behavioral symptoms (44%) were the most frequent complaint, while vomiting (11%) was the least common.
- Higher weekly MTX doses (20 mg) correlated with increased intolerance (46.2%), whereas lower doses (7.5 mg) showed reduced intolerance (20%).
- Concomitant use of other DMARDs did not significantly increase MTX intolerance.
Conclusions:
- Methotrexate intolerance is moderately prevalent in RA patients and is directly related to the MTX dose.
- Undetected MTX intolerance can lead to decreased patient compliance with first-line MTX therapy.
- The study suggests that MTX dosage adjustment, rather than avoidance of other DMARDs, may be key in managing MTX intolerance.
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