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Original Abstract of the Article

Major Research Findings

Propylthiouracil (PTU) is a commonly used drug for treating hyperthyroidism. Hyperthyroidism affects approximately 0.2% to 2.7% of all pregnancies and is generally treated with PTU. 1 PTU has been shown to be effective in treating hyperthyroidism during pregnancy, however, its effects on the mother and fetus are controversial. 1

Research using zebrafish found that PTU reduced thyroid hormone levels and increased sex hormone secretion. 16 This suggests that PTU may affect the interaction between endocrine systems by inhibiting the production of thyroid hormone and regulating the secretion of sex hormones. 16

PTU has been used to treat hyperthyroidism for over 50 years. 18 Compared to methimazole, PTU is the only thyrostatic drug approved by the American Academy of Pediatrics for mothers who are breastfeeding. 18 PTU is recommended for treating hyperthyroidism in pregnant women because it has a lower placental transfer rate compared to methimazole, although the effect on the newborn does not appear to be different from that of methimazole. 18

Research using rats found that hypothyroidism induced by PTU resulted in reduced testicular function, abnormal sperm, and decreased fertility. 9 Hypothyroidism caused by PTU lowered blood levels of testosterone, LH, and FSH, and increased blood levels of prolactin and cholesterol. 9

PTU may affect fetal development. 3 Research suggests that PTU may lead to fewer birth defects in newborns compared to methimazole and carbimazole. 3

PTU may affect brain development in rats. 8 Hypothyroidism caused by PTU altered dopamine and serotonin levels in the brain of rats. 7

PTU was shown to decrease antioxidant enzyme activity in rat hearts and increase lipid peroxidation. 25 These findings suggest that PTU may cause oxidative stress in the heart. 25

PTU may affect undescended testes in newborn rats. 22

PTU did not affect thyroid function in goldfish but it was shown that elevated thyroid hormone levels in goldfish can suppress appetite. 6

PTU has been shown to improve blood lipids in diabetic rats and hypothyroid rats. 14

PTU may cause oxidative stress in rat brain tissue and may impair learning and memory ability. 12

PTU may affect the immune system in rats. 20

PTU has been shown to reduce lipid peroxidation caused by potassium bromate, which can cause thyroid tumors. 24

PTU has been shown to increase the production of pregnenolone in rat granulosa cells. 17

PTU may lead to fewer birth defects in newborns compared to methimazole, when used to treat hyperthyroidism in pregnancy. 11

PTU may be more effective than methimazole in preventing atherosclerosis in patients with Graves' disease. 5

PTU may have a protective effect on thyroid gland tissue in rats. 2

PTU may reduce ischemia-reperfusion injury in rat kidneys. 13

PTU has been shown to reduce lipid peroxidation in thyroid tissue in rats. 15

PTU has been shown to prolong the duration of the P wave in patients with overt hyperthyroidism. 21

PTU has been shown to delay metamorphosis and affect thyroid gland histology in the European common frog. 4

PTU has been shown to inhibit the expression of iodotyrosine deiodinase 1 in thyroid cells. 10

Benefits and Risks

Benefit Summary

PTU may be effective in treating hyperthyroidism during pregnancy. 1 PTU is the only thyrostatic drug approved for breastfeeding mothers by the American Academy of Pediatrics. 18 PTU is recommended for treating hyperthyroidism in pregnancy as it has a lower placental transfer rate compared to methimazole. 18 PTU may be more effective in preventing atherosclerosis. 5

Risk Summary

PTU may cause reduced testicular function, abnormal sperm, and decreased fertility. 9 PTU may affect fetal development. 3 PTU may affect brain development in rats. 8 PTU may cause oxidative stress in the heart. 25 PTU may affect the immune system. 20 PTU has been shown to delay metamorphosis and affect thyroid gland histology in the European common frog. 4

Comparison of Studies

Commonalities

Many studies show that PTU inhibits the production of thyroid hormone. 16 18 9 3 8 25 22 6 14 12 20 24 17 11 5 2 13 15 21 4 10 Also, many studies have shown that PTU may have adverse effects on the mother and fetus. 1 16 9 3 8 25 22 12 20 4

Differences

There is no consensus on whether PTU is effective in treating hyperthyroidism during pregnancy. 1 There is also no consensus on the effects of PTU on birth defects in newborns. 3 11 There is also no consensus on the effects of PTU on brain development in rats. 8 7

Consistency and Inconsistencies of Results

More research is needed on the safety and effectiveness of PTU. 1 There is no consensus on the effects of PTU on the mother and fetus. 1 3 11

Notes on Real-World Applications

While PTU may be effective in treating hyperthyroidism during pregnancy, the potential effects on the mother and fetus should be considered. 1 PTU is the only thyrostatic drug approved for breastfeeding mothers but the effects on the newborn should be considered. 18 PTU may be more effective in preventing atherosclerosis, however, more research is needed. 5

Limitations of Current Research

There is still not enough research on the safety and effectiveness of PTU. 1 Research design and sample size are important when assessing the effects of PTU on the mother and fetus. 1 3 11

Future Research Directions

Long-term effects need to be investigated when assessing the safety and effectiveness of PTU. 1 Also, the effects of PTU on the mother and fetus need to be investigated in detail. 1 3 11

Conclusion

PTU is an effective drug for treating hyperthyroidism but the potential effects on the mother and fetus should be considered. 1 It is important to consult with your doctor and carefully consider the use of PTU. 1


Literature analysis of 25 papers
Positive Content
16
Neutral Content
2
Negative Content
7
Article Type
2
2
0
2
25

Language : English


Author: BhagatMehak, SinghPurnima, SunkaraSindhu Meghana, AbrahamMerin T, Barroso AlverdeMaria Jimena, MundlaSravya R, Mizrahi DrijanskiAndrea, JobilalAnna, LakkimsettiMohit, NairNandini, RazzaqWaleed, AbdinZain U, GuptaIshita


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