Content » Vol 91, Issue 1

Investigative Report

Isotretinoin Influences Pituitary Hormone Levels in Acne Patients

Ayse Serap Karadag1*, Derun Taner Ertugrul2*, Emre Tutal3 and Kadir Okhan Akin4

Department of 1Dermatology, Yuzuncu Yil University, Faculty of Medicine, Departments of 2Internal Medicine, Division of Endocrinology, 3Internal Medicine, and 4Biochemistry, Ankara Kecioren Research and Training Hospital, Ankara, Turkey

*These authors contributed equally to this article and should be considered as first authors.

Besides suppressing sebum production, the exact mechanism of action of isotretinoin in acne vulgaris is not known. Several hormones have been linked to the pathogenesis of acne. In this study, we investigated the effects of isotretinoin on the pituitary-adrenal axis, whose activity may be increased in acne. Various hormone systems were evaluated before and after 3 months of isotretinoin treatment in 47 acne patients. Free triiodothyronine (T3), thyroid-stimulating hormone and thyroid-stimulating hormone receptor antibody levels decreased significantly during isotretinoin treatment (p < 0.001, p < 0.02 and p < 0.02, respectively), as did those of luteinising hormone, prolactin and total testosterone (p < 0.005), as well as morning cortisol and adrenocorticotropic hormone (p < 0.005 and p < 0.05, respectively). We conclude that isotretinoin causes mild suppression of pituitary hormone levels, which may be beneficial for tackling the pathogenesis of acne. Key words: acne; hormone; isotretinoin; pituitary.

(Accepted September 10, 2010.)

Acta Derm Venereol 2011; 91: 31–34

Ayse Serap Karadag, MD, Department of Dermatology, Yuzuncu Yil University, Faculty of Medicine, Ankara, Turkey. E-mail:

Acne vulgaris is primarily a disease of the pilosebaceous unit. Four main pathogenic factors are known to lead to its development: (i) follicular epidermal hyperproliferation; (ii) excess sebum production; (iii) inflammation; and (iv) the presence and activity of Propionibacterium acnes. With the onset of puberty, androgen-mediated stimulation of the sebaceous gland results in increased sebum production (1). Several hormones implicated in the regulation of sebaceous gland activity have been linked to acne. They include androgens, estrogens, growth hormone, insulin, insulin-like growth factor-1 (IGF-1), corticotropin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), melanocortins and glucocorticoids (2). Individuals who are intrinsically insensitive to androgens do not produce sebum and do not develop acne. Conversely, conditions characterised by high androgen activity are often associated with acne formation. Thus, it is commonly believed that hypersensitivity of the sebaceous glands to androgens is the underlying cause of acne (3).

Proopiomelanocortin (POMC) is produced by the anterior pituitary gland in response to CRH released from the hypothalamus. A precursor polypeptide, its cleavage yields melanocortins, ACTH and melanocyte-stimulating hormone (MSH). Human sebocytes express the melanocortin receptors MC-1R and MC-5R through which ACTH and MSH produce various effects on the sebaceous gland (2–4). ACTH also stimulates the production of cortisol in the adrenal gland (5). It is well known that the use of topical or systemic glucocorticoids promotes acneiform eruptions. In vitro studies have demonstrated that hydrocortisone stimulates sebocyte proliferation in a dose-dependent manner, and that cortisol is essential for sebocyte differentiation, as well as GH- and IGF-1-induced sebocyte differentiation and IGF-1-mediated proliferation (6). These results suggest that steroids may induce acne by promoting sebocyte proliferation and differentiation (7).

Isotretinoin (ISO), a 13-cis-retinoic acid derivative of vitamin A, is a highly effective therapy for severe nodulocystic acne. Although its mechanism of action is not fully understood, ISO is thought to isomerise to all-trans-retinoic acid (ATRA) ISO, which then interacts with retinoid receptors (8).

The mechanism by which decreases sebum production is not well understood. Few published data describe its effects on hormone physiology in acne patients. In this study, we sought to investigate the effect of ISO on various hormone systems in acne patients.


A total of 47 patients with acne vulgaris (31/16 females/males; mean age 20.8 ± 3.5 years), who were admitted to our outpatient dermatology clinic between October 2009 and March 2010, were included in the study. The study group was selected from a group of male and non-pregnant female patients between the ages of 17 and 34 years with moderate to severe nodulocystic acne. Females at risk of becoming pregnant were advised to use barrier contraception methods (no hormonal contraception was allowed), and produced a negative serum pregnancy test one week before the initiation of ISO therapy. Treatment was commenced on the second or third day of the menstrual cycle in these patients. Patients using vitamin A supplements or satisfying any of the following criteria were excluded from the study: sensitivity or allergy to parabens; previously diagnosed thyroid or pituitary disease; recent history of psychiatric, mood or depressive disorders; and previous therapy with oral retinoids or hormone therapy for any reason in last 3 months. All patients gave their written informed consent, and the study was conducted according to GCP guidelines.

The study was approved by the local ethics committee and was conducted according to the ethical principles of the Declaration of Helsinki.

ISO therapy was initiated at a dose of 0.5–0.75 mg/kg body weight. The drug was administered twice daily with meals. Treatment was continued for at least 5 months. Biochemical parameters were screened immediately prior to initiation (pretreatment) and after 3 months of ISO treatment (posttreatment). These parameters were: free T3 (fT3), free T4 (fT4), thyroid-stimulating hormone (TSH), thyroglobulin, anti-thyroid peroxidase (anti-TPO) and anti-thyroglobulin (anti-Tg), thyroid-stimulating hormone receptor antibody (TRAb), 17-hydroxyprogesterone, progesterone, total and free testosterone, estradiol, luteinising hormone (LH), follicle-stimulating hormone (FSH), sex hormone-binding globulin (SHBG), dehydroepiandrosterone sulfate (DHEAS), cortisol, adrenocorticotropic hormone (ACTH), haemoglobin, creatinine, alanine aminotransferase (ALT) and aspartate aminotransferase (AST), total cholesterol, triglycerides, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), and very low-density lipoprotein cholesterol (VLDL-C). Fasting blood samples were obtained by venipuncture of the large antecubital veins, without stasis and after 12 hours’ fasting. Samples were centrifuged immediately; the plasma was separated and stored at –80°C. In order to limit undesired variation, all samples were studied on the same day and using the same kit. Fasting serum glucose, total cholesterol, triglyceride, LDL-C, HDL-C, ALT and AST concentrations were measured enzymatically using an automatic analyser (Konelab 60i; Thermo Fisher Scientific Inc. MA, USA). Total cholesterol and triglycerides were measured using colorimetric enzymatic tests, and LDL-C and HDL-C using an homogeneous enzymatic colorimetric test (Konelab 60i). Serum glucose levels were measured by the hexokinase method (Konelab 60i). fT3 (normal 2.2–4.2 pg/ml), fT4 (normal 0.65–1.7 ng/dl), TSH (normal 0.3–3.6 mIU/l), thyroglobulin (normal 0.2–70 ng/ml), anti-TPO (normal 1–500 IU/ml) and anti-Tg (normal 5–100 IU/ml), ACTH (normal 4.5–48.8 pg/ml) and DHEAS (normal 80.2–339.5 µg/dl) were measured using chemiluminescence methods (Liason®; Diasorin S.p.A., Saluggia, Vercelli, Italy). TRAb (normal 0–405 U/l) (Zentech S.A., Angleur, Belgium) (catalog no: R-CT-100), 17-hydoxyprogesterone (normal 0.61–3.34 ng/ml) and free testosterone (normal 0.02–3.09 pg/ml) (Diagnostic System Laboratory Inc., Texas, USA) were measured by radioimmunoassay.

Levels of estradiol (reference range 27–433 pg/ml), FSH (reference range 1.79–22.51 mIU/ml), LH (normal 0.2–250 mIU/ml), prolactin (normal 1.2–58.64 ng/ml), progesterone (normal 0.08–18.56 ng/ml), total testosterone (normal 0.1–0.75 ng/ml) and cortisol (normal 6.7–22.6 µg/dl) were measured using chemiluminescence methods (UniCel® DxI 800 Immunoassay System; Beckman Coulter Inc., Clinical Diagnostics Division, Brea, CA, USA), as were SHBG levels (normal 16–110 µmol/l) (Architect i2000sr; Abbott Laboratories, Medical Diagnostics Products, New Jersey, USA).

Statistical analyses were performed using SPSS software (Statistical Package for the Social Sciences version 15.0; SSPS Inc., Chicago, Il, USA). The normality of data was analysed using the Kolmogorov-Smirnov Test. All numerical variables following a normal distribution were expressed as the mean ± standard deviation (SD), while data that were not normally distributed were expressed as the median (interquartile range (IR)). The paired sample t-test was used to compare pretreatment and posttreatment values for hormonal and biochemical data with homogenic variability. The Wilcoxon signed-rank test was used to analyse data with skew distribution.


Comparisons of blood lipid and hepatic parameters before and after ISO treatment are summarised in Table I. We found that levels of total cholesterol, LDL-C, triglycerides (p < 0.0001, 0.0001 and 0.005, respectively), AST (p < 0.005) and ALT (p < 0.001) increased following treatment, while HDL-C levels (p < 0.0001) decreased, in accordance with previous findings (9, 10). There was no significant change in fasting blood glucose levels (p > 0.05). Comparisons of pre- and posttreatment hormonal parameters are summarised in Tables II and III. We found that levels of fT3, TSH and TRAb decreased significantly following ISO treatment (p < 0.001, 0.02 and 0.02, respectively). There were no significant changes in the levels of thyroglobulin, anti-Tg or anti-TPO after ISO treatment (Table II). With regard to estradiol, prolactin, progesterone, 17-hydroxyprogesterone, FSH and LH, we found that posttreatment LH and prolactin levels were significantly lower than pretreatment values (Table III), while there were no significant changes in the other hormonal parameters. Moreover, while there were no changes in free testosterone, DHEAS or SHBG levels, posttreatment total testosterone levels were also significantly lower than initial values (p < 0.005). Morning cortisol and ACTH levels were also significantly reduced following ISO treatment (p < 0.005 and 0.05, respectively).

Table I. Pre- and posttreatment values for biochemical parameters (n = 47)


Mean ± SD or

Median (IR)


Mean ± SD or

Median (IR)


Fasting blood glucose (mg/dl)

84.2 ± 8.4

87.0 ± 7.0

> 0.05

Total-C (mg/dl)

149.4 ± 37.5

162.4 ± 40.7

< 0.0001

LDL-C (mg/dl)

73.5 ± 23.0

93.0 ± 32.6

< 0.0001

HDL-C (mg/dl)

50.2 ± 14.2

46.7 ± 13.4

< 0.05

Triglyceride (mg/dl)

78.4 ± 31.7

191.9 ± 66.7

< 0.005

AST (mg/dl)

18.2 ± 4.9

24.6 ± 6.4

< 0.0001

ALT (mg/dl)

14.0 (10.0)

18.0 (14.0)

< 0.001

SD: standard deviation; Total-C: total cholesterol; LDL-C: low-density lipoprotein cholesterol; HDL-C: high-density lipoprotein cholesterol; AST: aspartate aminotransferase; ALT: alanine aminotransferase.

Table II. Thyroid function tests and related antibodies (n = 47)


Mean ± SD or

Median (IR)


Mean ± SD or

Median (IR)


fT3 (pg/ml)

3.3 ± 0.5

2.9 ± 0.4

< 0.001

fT4 (ng/dl)

1.0 ± 0.2

1.0 ± 0.2


TSH (mIU/l)

2.0 ± 0.8

1.7 ± 0.9

< 0.02

TRAb (U/l)

8.5 ± 1.3

8.1 ± 1.3

< 0.02

Thyroglobulin (ng/ml)

7.2 ± 4.6

7.5 ± 5.5


Anti-Tg (IU/ml)

5.4 (2.3)

5.0 (1.02)


Anti-TPO (IU/ml)

2.5 (3.3)

2.5 (2.4)


SD: standard deviation; fT3: free T3; fT4: free T4; TSH: thyroid-stimulating hormone; TRAb: thyroid-stimulating hormone receptor antibody; Anti-Tg: anti-thyroglobulin; Anti-TPO: anti-thyroid peroxidase.

Table III. Pre- and posttreatment evaluation of pituitary-adrenal axis and sex hormones (n = 47)


Mean ± SD or

Median (IR)


Mean ± SD or

Median (IR)


Estradiol (pg/ml)

84.0 (75.0)

67.0 (95.5)


FSH (mIU/ml)

6.0 ± 3.6

5.9 ± 2.5


LH (mIU/ml)

8.1 (11.6)

6.7 (6.0)

< 0.02

Prolactin (ng/ml)

13.3 ± 5.7

11.6 ± 4.4

< 0.02

Progesterone (ng/ml)

1.9 (3.8)

1.5 (2.6)


17-hydroxyprogesterone (ng/ml)

2.3 (2.1)

2.3 (2.2)


Total testosterone (ng/ml)

0.7 (0.4)

0.5 (0.4)

< 0.005

DHEAS (µg/dl)

217.6 ± 104.9

205.6 ± 80.0


Free testosterone (pg/ml)

2.9 (2.0)

2.5 (1.1)


SHBG (µmol/l)

40.6 ± 19.8

51.7 ± 34.1


Cortisol (μg/dl)

13.1 ± 5.2

11.0 ± 5.8

< 0.005

ACTH (pg/ml)

28.9 ± 17.0

24.9 ± 13.6

< 0.05

SD: standard deviation; FSH: follicle-stimulating hormone; LH: luteinising hormone; DHEAS: dehydroepiandrosterone sulfate; SHBG: sex hormone-binding globulin; ACTH: adrenocorticotropic hormone.

When we analyzed men and women seperately, posttreatment total testosterone levels were still significant (p = 0.003), however cortisol and LH levels lost their significance in women. In men, however, posttreatment levels of cortisol (p = 0.044), but not total testosterone (p = 0.063) or LH (p = 0.07), were lower than pretreatment values. These disparities may be related to the decrease in statistical power caused by dividing the study group into two subgroups.


In this study, we found that ISO treatment induced several changes in the hormonal status of acne patients: TSH, fT3, cortisol, ACTH, LH, total testosterone and prolactin levels declined significantly after 3 months of treatment (see Table III).

Very few clinical studies have investigated the effects of retinoids on pituitary hormone levels. Angioni et al. (11) studied the effects of the aromatic retinoid acitretin on pituitary hormone levels in eleven adult male psoriasis patients. They found significant decreases in TSH, fT3 and prolactin levels after treatment, consistent with our results. They did not, however, detect changes in cortisol, testosterone, LH or FSH levels, which may reflect the use of another retinoid and the smaller patient group in this study compared to our study.

To our knowledge, this is the first study investigating the effects of ISO on thyroid hormone levels. Decreases in TSH and fT3 levels may be caused by central hypothyroidism due to RXR-mediated suppression of TSHβ gene expression, as previously shown for bexarotene (12). However, it is unclear whether treatment of acne with ISO generates enough 9-cis-isomers to account for any RXR-mediated effect. Although the decrease in TRAb levels after ISO treatment was statistically significant, the size of the change (average 4%) may not be clinically important in individuals without thyroid disease.

It has been demonstrated that retinoids are able to induce the transcription of the dopamine receptor type 2 (D2R) gene in cultured pituitary cells, this effect being due to the presence of a functional retinoic acid response element (RARE) in the D2R promoter (13). The decrease in the levels of prolactin following ISO treatment may be related to an increase in central dopaminergic tonus. In a previous study, we showed that IGF-1 and IGFBP-3 levels also decrease following ISO treatment (14), responses that may also have stemmed from an increase in dopaminergic tonus.

Retinoic acid has been shown to inhibit proliferation and induce differentiation and apoptosis in different cell types (15). Some of these effects result from reduced binding of the transcription factors AP-1 and Nur77 to their cognate DNA sites (16, 17). These factors are also essential in the control of the POMC gene, which is the precursor for both ACTH and α-MSH (18–20). Páez-Pereda et al. (21) have shown that ATRA inhibits ACTH secretion both in vitro and in vivo through an effect on POMC transcription, and also inhibits ACTH-secreting tumour cell development and proliferation. They found that retinoic acid inhibits the transcriptional activity of AP-1 and the orphan receptors Nur77 and Nurr1 in ACTH-secreting tumour cells. They also showed that, in adrenal cortex cells, retinoic acid inhibits corticosterone production and cell proliferation. Castillo et al. (22), meanwhile, demonstrated the effectiveness of 9-cis retinoic acid for treating Cushing’s disease in dogs. We speculate that these molecular mechanisms may contribute to the observed decreases in the levels of both ACTH and cortisol following ISO treatment.

We do not know the reasons behind the declines in LH and total testosterone levels in our study. Few studies have investigated the effects of retinoids on androgen metabolism. One previous study reported decreases in the levels of testosterone and the precursor androgen androstenedione in 6/9 acne patients after 12 weeks of ISO therapy (23). However, these researchers did not observe a significant change in LH levels. In a laboratory study, ATRA was found to decrease both basal and LH-stimulated testosterone secretion in cultured testicular cells, these effect being mediated by RARα receptors (24).The decrease in testosterone levels may at least partly explain the effectiveness of this medication for treating acne. Androgens are important in the pathogenesis of acne because they enhance follicular keratosis and influence sebum production (25). Several studies have demonstrated hyperandrogenaemia in patients with acne vulgaris, typically in conjunction with other clinical signs of hyperandrogenism such as hirsutism, alopecia and/or menstrual disturbances. Estrogen treatments effectively combat acne by lowering levels of androgens, (25) and counteracting their effects on the sebaceous gland. Reducing testosterone levels may also be beneficial in polycystic ovary syndrome, in which hyperandrogenaemia is a well-known pathogenic mechanism.

In conclusion, we have shown in this study that short-term ISO treatment results in mild suppression of pituitary hormones. This effect may be related to the effectiveness of this medication in acne treatment. We propose that retinoids may be tested in the future in the treatment of different pituitary diseases.


  • George R, Clarke S, Thiboutot D. Hormonal therapy for acne. Semin Cutan Med Surg 2008; 27: 188–196.
  • Lolis MS, Bowe WP, Shalita AR. Acne and systemic disease. Med Clin North Am 2009; 93: 1161–1181.
  • Thiboutot D. Acne: hormonal concepts and therapy. Clin Dermatol 2004; 22: 419–428.
  • Zouboulis CC, Baron JM, Bohm M, Kippenberger S, Kurzen H, Reichrath J, et al. Frontiers in sebaceous gland biology and pathology. Exp Dermatol 2008; 17: 542–551.
  • Chrousos GP, Peck GL, Gross EG, Cutler GB Jr, Loriaux DL. Adrenal function in women with idiopathic acne. J Invest Dermatol 1982; 78: 468–471.
  • Deplewski D, Rosenfield RL. Growth hormone and insulin-like growth factors have different effects on sebaceous cell growth and differentiation. Endocrinology 1999; 140: 4089–4094.
  • Deplewski D, Rosenfield RL. Role of hormones in pilosebaceous unit development. Endocr Rev 2000; 21: 363–392.
  • DeLuca LM. Retinoids and their receptors in differentiation, embryogenesis and neoplasia. FASEB J 1991; 5: 2924–2933.
  • Tallab T, Joharji H, Jazei M, Bahamdan K, Ibrahim K, Karkashan E. Isotretinoin therapy: any need for laboratory assessment? West Afr J Med 2004; 23: 273–275.
  • Brelsford M, Beute TC. Preventing and managing the side effects of isotretinoin. Semin Cutan Med Surg 2008; 27: 197–206.
  • Angioni AR, Lania A, Cattaneo A, Beck-Peccoz P, Spada A. Effects of chronic retinoid administration on pituitary function. J Endocrinol Invest 2005; 28: 961–964.
  • Sherman SI, Gopal J, Haugen BR, Chiu AC, Whaley K, Nowlakha P, et al. Central hypothyroidism associated with retinoid X receptor-selective ligands. N Engl J Med 1999; 340: 1075–1079.
  • Samad TA, Krezel W, Chambon P, Borrelli E. Regulation of dopaminergic pathways by retinoids: activation of the D2 receptor promoter by members of the retinoic acid receptor-retinoid X receptor family. Proc Natl Acad Sci USA 1997; 94: 14349–14354.
  • Karadag AS, Ertugrul DT, Tutal E, Akin KO. Short-term isotretinoin treatment decreases insulin-like growth factor-1 and insulin-like growth factor-binding protein-3 levels: does isotretinoin affect growth hormone physiology? Br J Dermatol 2010; 162: 798–802.
  • Merino R, Hurle JM. The molecular basis of retinoid action in tumors. Trends Mol Med 2003; 9: 509–511.
  • Fanjul A, Dawson MI, Hobbs PD, Jong L, Cameron JF, Harlev E, et al. A new class of retinoids with selective inhibition of AP-1 inhibits proliferation. Nature 1994; 372: 107–111.
  • Kang HJ, Song MR, Lee SK, Shin EC, Choi YH, Kim SJ, et al. Retinoic acid and its receptors repress the expression and transactivation functions of Nur77: a possible mechanism for the inhibition of apoptosis by retinoic acid. Exp Cell Res 2000; 256: 545–554.
  • Kovalovsky D, Refojo D, Liberman AC, Hochbaum D, Pereda MP, Coso OA, et al. Activation and induction of NUR77/NURR1 in corticotrophs by CRH/cAMP: involvement of calcium, protein kinase A, and MAPK pathways. Mol Endocrinol 2002; 16: 1638–1651.
  • Maira M, Martens C, Philips A, Drouin J. Heterodimerization between members of the Nur subfamily of orphan nuclear receptors as a novel mechanism for gene activation. Mol Cell Biol 1999; 19: 7549–7557.
  • Philips A, Lesage S, Gingras R, Maira MH, Gauthier Y, Hugo P, et al. Novel dimeric Nur77 signaling mechanism in endocrine and lymphoid cells. Mol Cell Biol 1997; 17: 5946–5951.
  • Paez-Pereda M, Kovalovsky D, Hopfner U, Theodoropoulou M, Pagotto U, Uhl E, et al. Retinoic acid prevents experimental Cushing syndrome. J Clin Invest 2001; 108: 1123–1131.
  • Castillo V, Giacomini D, Paez-Pereda M, Stalla J, Labeur M, Theodoropoulou M, et al. Retinoic acid as a novel medical therapy for Cushing’s disease in dogs. Endocrinology 2006; 147: 4438–4444.
  • Palatsi R, Ruokonen A, Oikarinen A. Isotretinoin, tetracycline and circulating hormones in acne. Acta Derm Venereol 1997; 77: 394–396.
  • Livera G, Rouiller-Fabre V, Habert R. Retinoid receptors involved in the effects of retinoic acid on rat testis development. Biol Reprod 2001; 64: 1307–1314.
  • Katsambas AD, Dessinioti C. Hormonal therapy for acne: why not as first line therapy? facts and controversies. Clin Dermatol 2010; 28: 17–23.