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Clinical Factors Affecting the Serum Retention of a Teratogenic Etretinate after the Acitretin Administration

  • Jeong, Jong Heon (Department of Dermatology, Dongguk University Ilsan Hospital, School of Medicine) ;
  • Hyun, Gyu Hwan (College of Pharmacy, Seoul National University) ;
  • Park, Yu Jeong (Department of Dermatology, Dongguk University Ilsan Hospital, School of Medicine) ;
  • Kwon, Sung Won (College of Pharmacy, Seoul National University) ;
  • Lee, Ai-Young (Department of Dermatology, Dongguk University Ilsan Hospital, School of Medicine)
  • Received : 2022.05.18
  • Accepted : 2022.07.07
  • Published : 2022.11.01

Abstract

Etretinate, an acitretin metabolite, has a long retention duration in adipose tissues with a teratogenic potential. FDA advises a contraceptive period of at least three years after discontinuing acitretin. However, the effect of accumulated etretinate in adipose tissues on fetus is unknown. Although the teratogenic threshold for serum concentration of etretinate has been presented as higher than 2 ng/mL, that of acitretin is unknown. To examine factors affecting body retention of acitretin and etretinate, effects of acitretin dosage, acitretin-taking duration, elapsed time after stopping acitretin, age, sex, concomitant alcohol consumption, and foods and supplements rich in vitamin A intake on serum concentrations of acitretin and etretinate were analyzed in 14 acitretin-taken patients and 58 controls without taking acitretin or etretinate. Serum concentrations of acitretin, but not etretinate, tended to be inversely related to the discontinuation duration. They were also related to old age. Different from a published result that alcohol consumption could promote the metabolism of acitretin into etretinate, alcohol intake did not affect serum concentrations of etretinate. Unexpectedly, more frequent intake of vitamin A or provitamin A-rich food and supplements was associated with higher serum acitretin, whereas less frequent intake of vitamin A or provitamin A-rich food and supplements was associated with higher serum levels of etretinate in acitretin-taken patients. Despite preliminary data, inter-individual variations in serum retention of etretinate suggest the necessity of further research before applying the same guidelines to everyone to minimize unnecessary contraception.

Keywords

Acknowledgement

This research was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HP20C0131).

References

  1. Barbero, P., Lotersztein, V., Bronberg, R., Perez, M. and Alba, L. (2004) Acitretin embryopathy: a case report. Birth Defects Res. A Clin. Mol. Teratol. 70, 831-833. https://doi.org/10.1002/bdra.20078
  2. Bouvy, M. L., Sturkenboom, M. C., Cornel, M. C., De Jong-Van den Berg, L. T., Stricker, B. H. and Wesseling, H. (1992) Acitretin (Neotigason). A review of pharmacokinetics and teratogenicity and hypothesis on metabolic pathways. Pharm. Weekbl. Sci. 14, 33-37.
  3. de Die-Smulders, C. E., Sturkenboom, M. C., Veraart, J., van Katwijk, C., Sastrowijoto, P. and van der Linden, E. (1995) Severe limb defects and craniofacial anomalies in a fetus conceived during acitretin therapy. Teratology 52, 215-219. https://doi.org/10.1002/tera.1420520407
  4. DiGiovanna, J. J., Zech, L. A., Ruddel, M. E., Gantt, G. and Peck, G. L. (1989) Etretinate. Persistent serum levels after long-term therapy. Arch. Dermatol. 125, 246-251. https://doi.org/10.1001/archderm.1989.01670140098019
  5. Dunn, L. K., Gaar, L. R.,Yentzer, B. A., O'Neill, J. L. and Feldman, S. R. (2011) Acitretin in dermatology: a review. J. Drugs Dermatol. 10, 772-782.
  6. Geiger, J. M., Baudin, M. and Saurat, J. H. (1994) Teratogenic risk with etretinate and acitretin treatment. Dermatology 189, 109-116. https://doi.org/10.1159/000246811
  7. Grote, W., Harms, D., Janig, U., Kietzmann, H., Ravens, U. and Schwarze, I. (1985) Malformation of fetus conceived 4 months after termination of maternal etretinate treatment. Lancet 1, 1276.
  8. Guenther, L. C., Kunynetz, R., Lynde, C. W., Sibbald, R. G., Toole, J., Vender, R. and Zip, C. (2017) Acitretin use in dermatology. J. Cutan. Med. Surg. 21, 2S-12S.
  9. Kara Polat, A., Oguz Topal, I., Aslan Kayiran, M., Koku Aksu, A. E., Aytekin, S., Topaloglu Demir, F., Ozkok Akbulut, T., Kivanc Altunay, I., Ozkur, E. and Karadag, A. S. (2021) Drug survival and safety profile of acitretin monotherapy in patients with psoriasis: a multicenter retrospective study. Dermatol. Ther. 34, e14834.
  10. Katugampola, R. P. and Finlay, A. Y. (2006) Oral retinoid therapy for disorders of keratinization: single-centre retrospective 25 years' experience on 23 patients. Br. J. Dermatol. 154, 267-276. https://doi.org/10.1111/j.1365-2133.2005.06906.x
  11. Kochhar, D. M., Penner, J. D. and Minutella, L. M. (1989) Biotransformation of etretinate and developmental toxicity of etretin and other aromatic retinoids in teratogenesis bioassays. Drug Metab. Dispos. 17, 618-624.
  12. Kumar, A., Monif, T., Khuroo, A., Sasmal, D., Goswami, D. and Lahkar, V. K. (2011) Stability-indicating validation of acitretin and isoacitretin in human plasma by LC-ESI-MS/MS bioanalytical method and its application to pharmacokinetic analysis. Biomed. Chromatogr. 25, 680-688. https://doi.org/10.1002/bmc.1503
  13. Larsen, F. G., Jakobsen, P., Larsen, C. G., Kragballe, K. and NielsenKudsk, F. (1988) Pharmacokinetics of etretin and etretinate during long-term treatment of psoriasis patients. Pharmacol. Toxicol. 62, 159-165. https://doi.org/10.1111/j.1600-0773.1988.tb01865.x
  14. Larsen, F. G., Jakobsen, P., Eriksen, H., Gronhoj, J., Kragballe, K. and Nielsen-Kudsk, F. (1991) The pharmacokinetics of acitretin and its 13-cis-metabolite in psoriatic patients. J. Clin. Pharmacol. 31, 477-483.
  15. Larsen, F. G., Jakobsen, P., Knudsen, J., Weismann, K., Kragballe, K. and Nielsen-Kudsk, F. (1993) Conversion of acitretin to etretinate in psoriatic patients is influenced by ethanol. J. Invest. Dermatol. 100, 623-627. https://doi.org/10.1111/1523-1747.ep12472293
  16. Larsen, F. G., Steinkjer, B., Jakobsen, P., Hjorter, A., Brockhoff, P. B. and Nielsen-Kudsk, F. (2000) Acitretin is converted to etretinate only during concomitant alcohol intake. Br. J. Dermatol. 143, 1164-1169. https://doi.org/10.1046/j.1365-2133.2000.03883.x
  17. Lee, C. S. and Koo, J. (2005) A review of acitretin, a systemic retinoid for the treatment of psoriasis. Expert. Opin. Pharmacother. 6, 1725-1734. https://doi.org/10.1517/14656566.6.10.1725
  18. Ling, M. R. (1999) Acitretin: optimal dosing strategies. J. Am. Acad. Dermatol. 41, S13- S17. https://doi.org/10.1016/S0190-9622(99)70360-9
  19. Lynde, C. W., Kraft, J. N. and Lynde, C. B. (2011) Acitretin revisited. Skin Therapy Lett. 16, 1-4.
  20. Maier, H. and Honigsmann, H. (2001) Assessment of acitretin-treated female patients of childbearing age and subsequent risk of teratogenicity. Br. J. Dermatol. 145, 1028-1029. https://doi.org/10.1046/j.1365-2133.2001.04424.x
  21. Meyer, E., de Bersaques, J., Lambert, W. E., de Leenheer, A. P. and Kint, A. H. (1993) Skin, adipose tissue and plasma levels of acitretin with rare occurrence of esterified acitretin during long-term treatment. Acta Derm. Venereol. 73, 113-115. https://doi.org/10.2340/0001555573113115
  22. Pilkington, T. and Brogden, R. N. (1992) Acitretin. A review of its pharmacology and therapeutic use. Drugs 43, 597-627. https://doi.org/10.2165/00003495-199243040-00010
  23. Sarkar, R., Chugh, S. and Garg, V. K. (2013) Acitretin in dermatology. Indian J. Dermatol. Venereol. Leprol. 79, 759-771. https://doi.org/10.4103/0378-6323.120721
  24. Schwartz, J. B. (2007) The current state of knowledge on age, sex, and their interactions on clinical pharmacology. Clin. Pharmacol. Ther. 82, 87-96. https://doi.org/10.1038/sj.clpt.6100226
  25. Sharma, P., Soni, K., Guttikar, S., Singhal, P., Patela, D. P. and Shrivastav, P. S. (2012) Separation of all-trans- and 13-cis-isomers of acitretin on a reversed-phase column, optimization of stability conditions and their simultaneous quantitation in human plasma by liquid chromatography-tandem mass spectrometry. Anal. Methods 4, 791-806. https://doi.org/10.1039/c2ay05852a
  26. Shi, S. and Klotz, U. (2011) Age-related changes in pharmacokinetics. Curr. Drug Metab. 12, 601-610. https://doi.org/10.2174/138920011796504527
  27. Soares, M. M., Silva, M. A., Garcia, P. P. C., da Silva, L. S., da Costa, G. D., Araujo, R. M. A. and Cotta, R. M. M. (2019) Efect of vitamin A suplementation: a systematic review. Cien. Saude Colet. 24, 827-838. https://doi.org/10.1590/1413-81232018243.07112017
  28. Strobel, M., Tinz, J. and Biesalski, H.-K. (2007) The importance of beta-carotene as a source of vitamin A with special regard to pregnant and breastfeeding women. Eur. J. Nutr. 46 Suppl 1, 1-20. https://doi.org/10.1007/s00394-007-1001-z
  29. Sturkenboom, M. C., de Jong-Van Den Berg, L. T., van Voorst-Vader, P. C., Cornel, M. C., Stricker, B. H. and Wesseling, H. (1994) Inability to detect plasma etretinate and acitretin is a poor predictor of the absence of these teratogens in tissue after stopping acitretin treatment. Br. J. Clin. Pharmacol. 38, 229-235. https://doi.org/10.1111/j.1365-2125.1994.tb04346.x