Serum Level of Insulin-Like Growth Factor 1 in Patients with Acne Vulgaris Versus Healthy Subjects

authors:

avatar Elham Behrangi 1 , avatar Abbas Rasi 1 , avatar Parisa Navid 1 , avatar Behzad Dalvand 1 , avatar Zahra Azizian 1 , *

Iran University of Medical Sciences, Tehran, Iran

how to cite: Behrangi E, Rasi A, Navid P, Dalvand B, Azizian Z. Serum Level of Insulin-Like Growth Factor 1 in Patients with Acne Vulgaris Versus Healthy Subjects. J Skin Stem Cell. 2018;5(3):e79784. https://doi.org/10.5812/jssc.79784.

Abstract

Background:

Role of insulin-like growth factor 1 (IGF1) and contributing cancer risk has been shown in many studies. Hence, this study was performed to determine the serum level of IGF-1 in patients with acne vulgaris in comparison with healthy subjects.

Methods:

The current study was a case-control assessment performed on a sample of 102 subjects, including 51 known cases of acne and 51 healthy subjects (without acne as controls). Serum IGF-1 level was assessed and compared across the two groups.

Results:

Both groups were matched for age and gender (P > 0.05). The mean IGF-1 level was significantly (P = 0.0001) higher in the case group. There was a significant reverse correlation between age and serum IGF-1 level (P = 0.002, r = -0.417). Also, the mean serum IGF-1 level was significantly higher in males compared with females in the case group (P = 0.006). The severity and location of acne had no association with serum IGF-1 level (P > 0.05).

Conclusions:

Overall, according to the obtained results in this study, it may be concluded that rate of metabolism is increased in patients with acne. This finding suggests that nutrition-related lifestyle factors play a role in acne pathogenesis. Hence, modifications in these styles are recommended to control acne formation. Also, use of IGF-1-reducing drugs, such as metformin, may be useful for treatment of acne. However, this matter may be confirmed by future studies.

1. Background

Acne vulgaris is a chronic disease with numerous cosmetic, psychological, and spiritual problems leading to decreased quality of life among affected individuals (1-3).

In spite of many therapeutic options, the disease is considered as a challenging burden. Worldwide distribution of acne is different due to geographic and ethnic factors and frequency of known risk factors for acne in each region (3).

The most important etiology of acne is related to sex hormone increase in circulation and subsequently target organs (2). One of the other pathophysiological signs of acne is excess metabolic rate and basal metabolism (4, 5). Some of the most important etiologic foods in these categories are those with higher carbohydrate and fatty contents. Therefore, it has been proposed that consumption of foods with lower carbohydrate and fatty contents would reduce acne (6, 7).

In previous reports, evaluating the association between metabolism status and acne was performed without a definite conclusion and there are some controversies in this regard (8-13). One of the metabolic indicators is insulin-like growth factor 1 (IGF1). This mediator is especially integrated in the carbohydrate pathway. If the serum level of this mediator is increased, it would be an indicator of high metabolic rate. Regarding the bi-dimensional role of IGF-1 as a risk factor for some cancers, such as prostate cancer, and acne, the control of this substance may be more important to reduce the risk of cancers and it may be an indicator of tumors in patients with persistent acne with high serum IGF-1 levels (14). Use of insulin-sensitizing agents, such as metformin, may be useful in reduction of cancer risk (14-16). Hence, this study was performed to determine the serum level of IGF-1 in patients with acne vulgaris in comparison with healthy subjects.

2. Methods

The current study was a case-control assessment performed on a sample of 102 subjects, including 51 known cases of acne and 51 healthy subjects (without acne as controls), during years 2013 and 2014. The obtained data included age, gender, acne severity, acne location, and serum IGF1 level. Informed consent was obtained from the ethics committee of Iran University.

Patients with established acne according to existing medical documents and physical examinations in dermatology clinic of an academic hospital were included as the case group. Also, 51 healthy subjects among a larger population attending a training hospital in Tehran, Iran, participated in this study. Also, subjects, who were using insulin and/or oral glucose-lowering agents were excluded. The serum IGF-1 level was measured in both groups by sampling 2 mL of patients' serum. The used technique was the enzyme linked immunosorbent assay (ELISA) and all laboratory assessments were performed in a single lab center of the hospital.

Data from 102 subjects were analyzed using the SPSS software (version 18.0) (Statistical Procedures for Social Sciences; Chicago, Illinois, USA). Differences were tested by Chi-Square, Fisher's exact test, and independent sample-T tests and were considered statistically significant at P values of less than 0.05.

3. Results

The mean age of participants (± standard deviation) was 24.16 ± 5.03 years in the acne group and 25.67 ± 1.56 years in the healthy control group (P > 0.05). Forty-two patients (82.4%) in the case group and 39 subjects (76.5%) in the control group were female (P > 0.05). Acne was mild, moderate, and severe according to the global acne grading system (GAGS) in 15.7%, 52.9%, and 31.4% of subjects, respectively. The acne location was face only in 45.1%, face and shoulder in 11.8%, face and chest in 5.9%, face and back in 3.9%, face and arm in 3.9%, and also 29.4% had acne in more than two locations.

The mean IGF-1 level was significantly (P = 0.0001) higher in the case group (Figure 1). There was a significant reverse correlation between age and serum IGF-1 level (P = 0.002, r = -0.417). A similar correlation was not seen in the control group. Also, the mean serum IGF-1 level was significantly higher in males compared with females in the case group (P = 0.006). A similar association was not seen in the control group. The severity and location of acne had no association with serum IGF-1 level (P > 0.05).

Serum IGF-1 levels in acne and control group
Serum IGF-1 levels in acne and control group

4. Discussion

In the current survey, two groups of acne and healthy control groups were compared for serum IGF-1 level. The findings showed that serum IGF1 levels were significantly different between the two groups and serum level of IGF-1 was higher in the case group. However there was no association between acne severity and location and serum IGF1 level; male gender and younger age were significantly associated with higher serum IGF-1 level.

The obtained results were similar to those reported by Vora et al. (9) in the United Kingdom, demonstrating a significant relationship between acne and sebum secretion with serum IGF-1 level. Also, Smith et al. (10) in Australia showed a similar association between acne and serum IGF1 level. However, Kaymak et al. (11) reported no significant difference between serum IGF1 levels in the two groups of patients with and without acne. Their results were not in congruence with the current findings. This difference may be due to cultural and dietary differences and calories intake between countries.

In some previous molecular studies, it was proposed that IGF1 would act in two ways for increasing acne formation; firstly, by increasing lipid peroxidation in sebaceous cells (resulting in more sebum secretion) and secondly increasing the sex hormone level. According to these pathophysiological theories, the current results are logical (6). Some authors recommend diets that reduce the production of sex hormones and also IGF1. On the other hand, some studies have shown that DHEA restores low circulating androgens in females into the normal range and increases IGF-1 levels. This theory suggests a negative feedback leading to an increased acne formation (12, 13).

Since there was a statistically significant association between acne and serum IGF1 level, it may be concluded that patients with acne have higher metabolism rate in comparison with the control group. This finding suggests that nutrition-related lifestyle factors play a role in acne pathogenesis. Hence, performing some modifications in these styles are recommended to control acne formation. Also, use of IGF-1-reducing drugs, such as metformin, may be useful in treatment of acne. However, this matter may be confirmed by future studies. In case of high IGF-1, focus on factors that inhibit IGF-1 may be suggested, such as fasting, Carbs (especial carbohydrates), protein restriction, calorie restriction, intense walking, legumes, royal jelly, glucosamine, bilberry, luteolin, curcumin, resveratrol, lycopene, green tea, boron, genistein (17-20). Restriction in use of materials, such as blueberry, vitamin C, calcium, red meat, fat, magnesium, zinc, carnitine, selenium, cinnamon, is also suggested (21).

References

  • 1.

    Hassan J, Grogan S, Clark-Carter D, Richards H, Yates VM. The individual health burden of acne: appearance-related distress in male and female adolescents and adults with back, chest and facial acne. J Health Psychol. 2009;14(8):1105-18. [PubMed ID: 19858331]. https://doi.org/10.1177/1359105309342470.

  • 2.

    Tan JK. Psychosocial impact of acne vulgaris: evaluating the evidence. Skin Therapy Lett. 2004;9(7):1-3. 9. [PubMed ID: 15334275].

  • 3.

    Sinclair W, Jordaan HF, Global Alliance to Improve Outcomes in Acne. Acne guideline 2005 update. S Afr Med J. 2005;95(11 Pt 2):881-92. [PubMed ID: 16344888].

  • 4.

    Thiboutot D. Acne: hormonal concepts and therapy. Clin Dermatol. 2004;22(5):419-28. [PubMed ID: 15556729]. https://doi.org/10.1016/j.clindermatol.2004.03.010.

  • 5.

    Danby FW. [Acne and diet]. Ann Dermatol Venereol. 2008;135(1):9-11. [PubMed ID: 18342067]. https://doi.org/10.1016/j.annder.2007.11.004.

  • 6.

    Smith RN, Mann NJ, Braue A, Makelainen H, Varigos GA. The effect of a high-protein, low glycemic-load diet versus a conventional, high glycemic-load diet on biochemical parameters associated with acne vulgaris: a randomized, investigator-masked, controlled trial. J Am Acad Dermatol. 2007;57(2):247-56. [PubMed ID: 17448569]. https://doi.org/10.1016/j.jaad.2007.01.046.

  • 7.

    Cordain L, Eades MR, Eades MD. Hyperinsulinemic diseases of civilization: more than just Syndrome X. Comp Biochem Physiol A Mol Integr Physiol. 2003;136(1):95-112. [PubMed ID: 14527633]. https://doi.org/10.1016/S1095-6433(03)00011-4.

  • 8.

    Khunger N, Iadvl Task Force. Standard guidelines of care for acne surgery. Indian J Dermatol Venereol Leprol. 2008;74 Suppl:S28-36. [PubMed ID: 18688101].

  • 9.

    Vora S, Ovhal A, Jerajani H, Nair N, Chakrabortty A. Correlation of facial sebum to serum insulin-like growth factor-1 in patients with acne. Br J Dermatol. 2008;159(4):990-1. [PubMed ID: 18652583]. https://doi.org/10.1111/j.1365-2133.2008.08764.x.

  • 10.

    Smith R, Mann N, Makelainen H, Roper J, Braue A, Varigos G. A pilot study to determine the short-term effects of a low glycemic load diet on hormonal markers of acne: a nonrandomized, parallel, controlled feeding trial. Mol Nutr Food Res. 2008;52(6):718-26. [PubMed ID: 18496812]. https://doi.org/10.1002/mnfr.200700307.

  • 11.

    Kaymak Y, Adisen E, Ilter N, Bideci A, Gurler D, Celik B. Dietary glycemic index and glucose, insulin, insulin-like growth factor-I, insulin-like growth factor binding protein 3, and leptin levels in patients with acne. J Am Acad Dermatol. 2007;57(5):819-23. [PubMed ID: 17655968]. https://doi.org/10.1016/j.jaad.2007.06.028.

  • 12.

    Smith TM, Cong Z, Gilliland KL, Clawson GA, Thiboutot DM. Insulin-like growth factor-1 induces lipid production in human SEB-1 sebocytes via sterol response element-binding protein-1. J Invest Dermatol. 2006;126(6):1226-32. [PubMed ID: 16575389]. https://doi.org/10.1038/sj.jid.5700278.

  • 13.

    Cappel M, Mauger D, Thiboutot D. Correlation between serum levels of insulin-like growth factor 1, dehydroepiandrosterone sulfate, and dihydrotestosterone and acne lesion counts in adult women. Arch Dermatol. 2005;141(3):333-8. [PubMed ID: 15781674]. https://doi.org/10.1001/archderm.141.3.333.

  • 14.

    Furstenberger G, Senn HJ. Insulin-like growth factors and cancer. Lancet Oncol. 2002;3(5):298-302. [PubMed ID: 12067807]. https://doi.org/10.1016/S1470-2045(02)00731-3.

  • 15.

    Boyd DB. Insulin and cancer. Integr Cancer Ther. 2003;2(4):315-29. [PubMed ID: 14713323]. https://doi.org/10.1177/1534735403259152.

  • 16.

    Pollack MN. Insulin, insulin-like growth factors, insulin resistance, and neoplasia. Am J Clin Nutr. 2007;86(3):s820-2. [PubMed ID: 18265475]. https://doi.org/10.1093/ajcn/86.3.820S.

  • 17.

    Kaklamani VG, Linos A, Kaklamani E, Markaki I, Koumantaki Y, Mantzoros CS. Dietary fat and carbohydrates are independently associated with circulating insulin-like growth factor 1 and insulin-like growth factor–binding protein 3 concentrations in healthy adults. J Clin Oncol. 1999;17(10):3291-8. https://doi.org/10.1200/jco.1999.17.10.3291.

  • 18.

    Levine ME, Suarez JA, Brandhorst S, Balasubramanian P, Cheng CW, Madia F, et al. Low protein intake is associated with a major reduction in IGF-1, cancer, and overall mortality in the 65 and younger but not older population. Cell Metab. 2014;19(3):407-17. [PubMed ID: 24606898]. [PubMed Central ID: PMC3988204]. https://doi.org/10.1016/j.cmet.2014.02.006.

  • 19.

    Kim T, Chang JS, Kim H, Lee KH, Kong ID. Intense Walking Exercise Affects Serum IGF-1 and IGFBP3. J Lifestyle Med. 2015;5(1):21-5. [PubMed ID: 26528426]. [PubMed Central ID: PMC4608228]. https://doi.org/10.15280/jlm.2015.5.1.21.

  • 20.

    El-Bahr SM. Curcumin regulates gene expression of insulin like growth factor, B-cell CLL/lymphoma 2 and antioxidant enzymes in streptozotocin induced diabetic rats. BMC Complement Altern Med. 2013;13:368. [PubMed ID: 24364912]. [PubMed Central ID: PMC3877970]. https://doi.org/10.1186/1472-6882-13-368.

  • 21.

    Crowe FL, Key TJ, Allen NE, Appleby PN, Roddam A, Overvad K, et al. The association between diet and serum concentrations of IGF-I, IGFBP-1, IGFBP-2, and IGFBP-3 in the European Prospective Investigation into Cancer and Nutrition. Cancer Epidemiol Biomarkers Prev. 2009;18(5):1333-40. [PubMed ID: 19423514]. https://doi.org/10.1158/1055-9965.EPI-08-0781.