Preview

Meditsinskiy sovet = Medical Council

Advanced search

Adverse effects of systemic acne therapy: A strategy of never giving up

https://doi.org/10.21518/ms2026-101

Abstract

The management of acne patients treated with isotretinoin has evolved quite markedly over the last years: from simply reporting elevated transaminase levels and lipids to a deeper insight into the mechanisms of these changes, development of effective correction methods, and to more clarity on patient selection criteria. Comorbid conditions that can affect safety and tolerability of systemic retinoids require special consideration. This article presents a clinical case of a 15-year-old female patient with severe, extensive, and treatment-resistant acne (IGA 4). The patient had been suffering from rashes over her face, chest, and back for three years. Her comorbidities included class I obesity (BMI 31.2), insulin resistance, hyperprolactinemia, and functional menstrual cycle disorders. The patient had a history of apathy and depressive episodes (she was emotionally stable at the time of therapy). The previous therapy with antiseptics and topical antibiotics has proved to be ineffective. Given the resistance and severity of the disease, isotretinoin was prescribed at a starting dose of 30 mg/day (0.36 mg/kg/day). After one month, improvements were noted: a decrease in sebum secretion and the number of inflammatory lesions. At 2.5 month of therapy, acute abdominal pain syndrome developed due to dietary inconsistency. Laboratory tests showed elevated transaminase levels (ALT, AST), and the abdominal ultrasound examination revealed signs of cholelithiasis. The acute condition was resolved. The isotretinoin dosage was temporally tapered to 10 mg/day, and a diet was recommended. After laboratory parameters and clinical status returned to normal, the dosage was gradually increased to 20 mg/day, and then to the initial therapeutic dose (30 mg/day). At the time of this writing, the patient was completing a course of isotretinoin therapy; the skin process regressed with development of stable clinical remission. The presented case demonstrates the potential to safely continue isotretinoin therapy with transient transaminase elevations, including in patients with comorbidities. Isotretinoin tapering, dietary therapy, and follow-up laboratory monitoring allow to maintain commitment to the treatment and achieve the target cumulative dose without discontinuation of the drug therapy.

About the Authors

O. А. Katkhanova
Klinika Mir-O-Med; Klinika Ekaterininskaya
Russian Federation

Olga A. Katkhanova, Dr. Sci. (Med.), Dermatovenerologist, Cosmetologist; Dermatovenerologist, Cosmetologist 

132, Rashpilevskaya St., Krasnodar, 350000;
37/1, Kubanskaya Naberezhnaya St., Krasnodar, 350063



M. Yu. Martynova
Kuban State Medical University
Russian Federation

Margarita Yu. Martynova, Student 

4, Mitrofan Sedin St., Krasnodar, 350063



References

1. Reynolds RV, Yeung H, Cheng CE, Cook-Bolden F, Desai SR, Druby KM et al. Guidelines of care for the management of acne vulgaris. J Am Acad Dermatol. 2024;90(5):1006.e1–1006.e30. https://doi.org/10.1016/j.jaad.2023.12.017.

2. Feszak IJ, Brzeziński P, Feszak S, Kitowska A, Waśkow M, Kawczak P, Bączek T. Isotretinoin Treatment for Acne Vulgaris: A Five-Year Retrospective Analysis of Clinical and Biochemical Adverse Effects. J Clin Med. 2025;14(18):6473. https://doi.org/10.3390/jcm14186473.

3. Eichenfield DZ, Sprague J, Eichenfield LF. Management of Acne Vulgaris: A Review. JAMA. 2021;326(20):2055–2067. https://doi.org/10.1001/jama.2021.17633.

4. Bagatin E, Costa CS. The use of isotretinoin for acne – an update on optimal dosing, surveillance, and adverse effects. Expert Rev Clin Pharmacol. 2020;13(8):885–897. https://doi.org/10.1080/17512433.2020.1796637.

5. Ruchitha S, Gupta N, Singh K. Exploring the multifaceted side effects of isotretinoin: a deep dive into case reports and observational studies. Arch Dermatol Res. 2025;317(1):499. https://doi.org/10.1007/s00403-025-04019-y.

6. Perlamutrov YuN, Olkhovskaya KB. Clinical effectiveness and safety profile of systemic isotretinoin in acne therapy. Klinicheskaya Dermatologiya i Venerologiya. 2020;19(5):730–736. (In Russ.) https://doi.org/10.17116/klinderma202019051730.

7. Fernández-Crehuet P, Fernández-Crehuet JL, Allam MF, Fernández-Crehuet Navajas R. Hepatotoxicity of isotretinoin in patients with acne and Gilbert’s syndrome: a comparative study. BMJ Open. 2014;4(3):e004441. https://doi.org/10.1136/bmjopen-2013-004441.

8. Wang JI, Jackson TL Jr, Kaplan DL. Isotretinoin-associated normalization of hyperbilirubinemia in patients with Gilbert’s syndrome. J Am Acad Dermatol. 1995;32(1):136–138. https://doi.org/10.1016/0190-9622(95)90216-3.

9. Gollnick H, Abanmi AA, Al-Enezi M, Al Hammadi A, Galadari I, Kibbi AG, Zimmo S. Managing acne in the Middle East: consensus recommendations. J Eur Acad Dermatol Venereol. 2017;31(Suppl. 7):4–35. https://doi.org/10.1111/jdv.14491.

10. Ortiz de la Torre M, Paternina González IY, Basurto IN, Vera Pinares MA, Chanona BK, Cabrera EM et al. Biochemical Monitoring During Isotretinoin Treatment: Review of International Guidelines and Recent Evidence. Int J Med Sci Clin Res Studies. 2026;6(2):247–256. https://doi.org/10.47191/ijmscrs/v6-i2-07.

11. Alrasheed AA, Alsadhan KF, Alfawzan NF, AbuDujain NM, Alnasser AH, Almousa H. Impact of Isotretinoin on Blood Lipids and Liver Enzymes: A Retrospective Cohort Study in Saudi Arabia. Ther Clin Risk Manag. 2024;20:567–575. https://doi.org/10.2147/TCRM.S466113.

12. Tawanwongsri W, Kanchanasuwan T, Eden C. Isotretinoin and Hepatotoxicity in Patients with Acne: A Narrative Review. Cosmetics. 2025;12(1):17. https://doi.org/10.3390/cosmetics12010017.

13. Alzoubi KH, Khabour OF, Hassan RE, Qarqaz F, Al-Azzam S, Mhaidat N. The effect of genetic polymorphisms of RARA gene on the adverse effects profile of isotretinoin-treated acne patients. Int J Clin Pharmacol Ther. 2013;51(8):631–640. https://doi.org/10.5414/CP201874.

14. Garcia-Cortes M, Robles-Diaz M, Stephens C, Ortega-Alonso A, Lucena MI, Andrade RJ. Drug induced liver injury: an update. Arch Toxicol. 2020;94(10):3381–3407. https://doi.org/10.1007/s00204-020-02885-1.

15. Lee YH, Scharnitz TP, Muscat J, Chen A, Gupta-Elera G, Kirby JS. Laboratory Monitoring During Isotretinoin Therapy for Acne: A Systematic Review and Meta-analysis. JAMA Dermatol. 2016;152(1):35–44. https://doi.org/10.1001/jamadermatol.2015.3091.

16. Barbieri JS, Shin DB, Wang S, Margolis DJ, Takeshita J. The clinical utility of laboratory monitoring during isotretinoin therapy for acne and changes to monitoring practices over time. J Am Acad Dermatol. 2020;82(1):72–79. https://doi.org/10.1016/j.jaad.2019.06.025.

17. Park YJ, Shin HY, Choi WK, Lee AY, Lee SH, Hong JS. Optimal laboratory testing protocol for patients with acne taking oral isotretinoin. World J Clin Cases. 2023;11(11):2435–2442. https://doi.org/10.12998/wjcc.v11.i11.2435.

18. Emtenani S, Abdelghaffar M, Ludwig RJ, Schmidt E, Kridin K. Risk and timing of isotretinoin-related laboratory disturbances: a population-based study. Int J Dermatol. 2024;63(12):1740–1747. https://doi.org/10.1111/ijd.17225.

19. Öktem A, Hayran Y, Arı E, Yalçın B. Minimize the regular laboratory monitoring during the systemic isotretinoin treatment: data of 704 patients with acne vulgaris. J Dermatolog Treat. 2019;30(8):813–817. https://doi.org/10.1080/09546634.2019.1591578.

20. Alajaji A, Alrawaf FA, Alosayli SI, Alqifari HN, Alhabdan BM, Alnasser MA. Laboratory Abnormalities in Acne Patients Treated With Oral Isotretinoin: A Retrospective Epidemiological Study. Cureus. 2021;13(10):e19031. https://doi.org/10.7759/cureus.19031.

21. Abd-Elaziz E, El-Kamshoushy AE, Sherif A, Wahdan I. Oral Isotretinoin and its Association with Liver Functions and Cholesterol Level among Acne Patients. J High Inst Public Health. 2020;50(1):25–31. https://doi.org/10.21608/jhiph.2020.81221.

22. Pona A, Cardenas-de la Garza JA, Haidari W, Cline A, Feldman SR, Taylor SL. Abnormal liver function tests in acne patients receiving isotretinoin. J Dermatolog Treat. 2021;32(4):469–472. https://doi.org/10.1080/09546634.2019.1662882.

23. Vieira AS, Beijamini V, Melchiors AC. The effect of isotretinoin on triglycerides and liver aminotransferases. An Bras Dermatol. 2012;87(3):382–387. https://doi.org/10.1590/s0365-05962012000300005.

24. Sibi Krishna T, Kaur R, Malhotra V, Fatima Z, Mustajab M, Singh T et al. The Impact of Isotretinoin on Lipid Profile: a Systematic Review. Ann Med Surg. 2025;87(7):4395–4403. https://doi.org/10.1097/MS9.0000000000003366.

25. Saylam Kurtipek G, Sarı N, Tuncez Akyurek F. Significant reduction in bilirubin levels in a patient with Gilbert’s Syndrome under isotretinoin treatment for acne vulgaris: A new area of use for isotretinoin? Dermatol Ther. 2019;32(3):e12884. https://doi.org/10.1111/dth.12884.

26. Gupta N, Ray M, Shayya A, McGinnis S, Marson J, Jagdeo J. Isotretinoin Does Not Increase the Risk of Inflammatory Bowel Disease: A TriNetX Retrospective Cohort Analysis. J Drugs Dermatol. 2025;24(12):1168–1172. https://doi.org/10.36849/JDD.9168.

27. Dancygier H. Drug- and toxin-induced liver injury. In: Clinical Hepatology: Principles and Practice of Hepatobiliary Diseases. Springer: Berlin/Heidelberg, Germany; 2010. Vol. 2, pp. 1223–1231.

28. Caruana DM, Wylie G. ’Washout’ period for oral tetracycline antibiotics prior to systemic isotretinoin. Br J Dermatol. 2016;174(4):929–930. https://doi.org/10.1111/bjd.14294.

29. Arowojolu AO, Gallo MF, Lopez LM, Grimes DA. Combined oral contraceptive pills for treatment of acne. Cochrane Database Syst Rev. 2012;2012(7):CD004425. https://doi.org/10.1002/14651858.CD004425.pub6.

30. Ledentsova SS, Gulyaev NI, Gordienko AV, Gavrilova NP, Oreshko LS, Seliverstov PV. Combination of acne treatment in women with prevention of complications using standard schemes of systemic retinoids. Lechaschi Vrach. 2020;(6):85–88. (In Russ.) https://doi.org/10.26295/OS.2020.30.33.015.

31. Layton A. The use of isotretinoin in acne. Dermatoendocrinol. 2009;1(3):162–169. https://doi.org/10.4161/derm.1.3.9364.

32. Baytyakov VV, Vlasova SA. Significance of insulin and insulin-like growth factor-1 in the pathogenesis of acne. Kazan Medical Journal. 2023;104(2):236–241. (In Russ.) https://doi.org/10.17816/KMJ112094.

33. Moscona-Nissan A. Concomitant isotretinoin therapy and whey protein supplementation: an underreported and hepatotoxic combination in adolescents – Literature Review. Academia Lett. 2021;(June):1277. https://doi.org/10.20935/AL1277.

34. Paschalidou E, Katsaras G, Papoulakis T, Kalloniati E, Kavvadas D, Karachrysafi S et al. The Effect of Isotretinoin on Insulin Resistance and Serum Adiponectin Levels in Acne Vulgaris Patients: A Systematic Review and Meta-Analysis. Clin Pract. 2024;14(3):1021–1037. https://doi.org/10.3390/clinpract14030081.

35. Cemil BC, Ayvaz HH, Ozturk G, Ergin C, Akıs HK, Gonul M et al. Effects of isotretinoin on body mass index, serum adiponectin, leptin, and ghrelin levels in acne vulgaris patients. Postepy Dermatol Alergol. 2016;33(4):294–299. https://doi.org/10.5114/pdia.2016.56928.

36. Endres LM, Bungau AF, Tit DM, Bungau GS, Radu A, Diaconu CC, Marin RC. Acne Vulgaris Associated with Metabolic Syndrome: A Three-Case Series Highlighting Pathophysiological Links and Therapeutic Challenges. Diagnostics. 2025;15(16):2018. https://doi.org/10.3390/diagnostics15162018.

37. Kruglova LS, Gryazeva NV, Tairova NA. Efficacy of Combined Administration of Systemic Isotretinoin and Omega-3 in Patients with Acne. Effective Pharmacotherapy. 2024;20(28):62–66. (In Russ.) Available at: https://umedp.ru/articles/effektivnost_sovmestnogo_priema_sistemnogo_izotretinoina_i_omega3_u_patsientov_s_akne.html.

38. Reyes-Hadsall S, Ju T, Keri JE. Use of Oral Supplements and Topical Adjuvants for Isotretinoin-Associated Side Effects: A Narrative Review. Skin Appendage Disord. 2024;10(1):1–9. https://doi.org/10.1159/000533963.


Review

For citations:


Katkhanova OА, Martynova MY. Adverse effects of systemic acne therapy: A strategy of never giving up. Meditsinskiy sovet = Medical Council. 2026;(2):116-124. (In Russ.) https://doi.org/10.21518/ms2026-101

Views: 53

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2079-701X (Print)
ISSN 2658-5790 (Online)