Table 2 |
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Studies on the use of the OCP and postmenopausal hormones and the risk of SLE |
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Type of study |
Comments |
Reference |
|
|
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|
Case-control |
Little or no association |
[41] |
|
Little association between SLE and current use or duration of use of hormone replacement therapy or OCP |
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|
No association with previous use of fertility drugs |
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|
Prospective cohort |
Slightly increased risk |
[84] |
|
OCP use: relative risk = 1.4 (95% CI = 0.9 to 2.1) |
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|
Duration of OCP use or time since first use did not increase the risk |
||
|
Case-control |
Increased risk (current oestrogen users with exposure >2 years) |
[85] |
|
SLE: odds ratio = 2.8 (95% CI = 0.9 to 9.0) |
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|
Discoid lupus: odds ratio = 2.8 (95% CI = 1.0 to 8.3) |
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|
When all cases were combined there was a difference between long-term users of oestrogen only (odds ratio = 5.3, 95% CI = 1.5 to 18.6) and those who used oestrogens combined with progestogens (odds ratio = 2.0, 95% CI = 0.8 to 5.0) when compared with nonusers |
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|
Prospective cohort |
Increased risk |
[28] |
|
OCP use: relative risk = 1.5 (95% CI = 1.1 to 2.1) |
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|
Postmenopausal hormones: relative risk = 1.9 (95% CI = 1.2 to 3.1) |
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|
|
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|
CI, confidence interval; OCP, oral contraceptive pill; SLE, systemic lupus erythematosus. |
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Oliver and Silman Arthritis Research & Therapy 2009 11:252 doi:10.1186/ar2825 |
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