AJMB

Association of Serotonin Transporter Gene Polymorphism with Recurrent Aphthous Stomatitis

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PMID: 29296268 (PubMed) - PMCID: PMC5742655 - View online: PubReader
Volume 10, Issue 1, January-March , Page 56 to 60
Monday, January 30, 2017 :Received , Wednesday, April 19, 2017 :Accepted


  • - Faculty of Dentistry, Tehran University of Medical Sciences, Tehran, Iran
    - International Campus, Dental Research Center, Tehran University of Medical Sciences, Tehran, Iran
  • Corresponding author Faculty of Dentistry, Tehran University of Medical Sciences, Tehran, Iran, Tel: +98 9127101007, Fax: +98 21 88335803, E-mail: amirabbaszahedi@yahoo.com
    - Faculty of Dentistry, Tehran University of Medical Sciences, Tehran, Iran

  • - Farabi Eye Hospital, Farabi Research Center, Tehran University of Medical Sciences, Tehran, Iran

  • - Research Center for Immunodeficiencies, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    - Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
    - Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Boston, MA, USA

Abstract:

Background: Recurrent Aphthous Stomatitis (RAS) is one of the most common diseases of the oral cavity all over the world (5-66%). RAS has a multifactorial etiology, while psychological factors such as stress and anger play a role in its manifestation. The serotonergic mechanisms particularly the serotonin-transporter gene (5-HTT) may affect the risk of psychological alterations and stress response. The aim of the present study was to evaluate the polymorphism of the promoter region of 5-HTT (5-HTTLPR) in the patients with RAS, compared to that in the control subjects.
Methods: In this case-control study, 100 patients with RAS and 100 healthy subjects were enrolled. PCR was performed on DNA of the samples, using a pair of primers capable of distinguishing S/L alleles and replicating 5-HTTLPR.
Results: No statistically significant difference existed between LL and LS genotype frequencies in the case and control groups. However, SS genotype frequency was significantly higher in the case group, as compared to the control group (p=0.001).
Conclusion: The conclusion of the present study demonstrated that S allele could approximately double the risk of RAS.


 

 

Introduction :

One of the most common oral diseases all over the world is Recurrent Aphthous Stomatitis (RAS) 1. This disease is characterized by aphthous ulcers recurring in oral mucosa 2. Unlike erosion, loss of continuity involves the whole epithelium and may affect the underlying connective tissue 3. The prevalence of RAS varies greatly among different populations 4,5. According to recent studies, it is estimated to vary between 5 and 66% with a mean of 20% 6.
Although its exact etiology remains obscure, RAS is known to be a multifactorial disorder 7. Many local and systemic factors are related to RAS. Some studies have suggested that the defects of the immune system could associate with this disease 8. The investigations have indicated that RAS may have immunological, psychological, genetic, and microbial bases 9,10. For instance, the levels of depression, anxiety, and stress in the patients suffering from RAS were specified using Hamilton Anxiety and Depression Scale (HADS) 11. In spite of contradictory findings, the psychological factors are considered to be involved in the pathogenesis of RAS 11-13. Moreover, 46% of the patients showed a positive familial history of this disorder in a study 14, which indicated the genetic role in its pathogenesis.
Approximately, 46% of the patients show a positive familial history 15. A variety of causes can play a role in RAS etiology such as local trauma, iron deficiency anemia, folic acid deficiency, vitamin B12 resorption defect 16, neutropenia 17, and such psychological factors as stress and anger 13. 
Noticeable evidence has demonstrated that psychological alterations in RAS may be influenced by the serotonergic mechanisms particularly serotonin-transporter gene (5-HTT) 18-20. The 5-HTT gene modulates the intensity and duration of serotonergic neurotransmission.Thus, this gene polymorphism can influence the anxiety related behaviors 21-24.
The 5-HTT gene (SLC6A4) is located on chromosome 17q12; it spans 31 kilobases (kb), and contains 14 exons 25,26. Two polymorphic regions have been known on SLC6A4 which are the 44-base pair (bp) insertion/deletion polymorphism within the promoter region (5-HTTLPR), and the 17-bp Variable Number of Tandem Repeat (VNTR) polymorphism in intron 2 19,25,26. Two allelic variants, a long (L) 16-repeat allele and a short (S) 14-repeat allele, could be detected on the first polymorphic region (5-HTTLPR) 26. It has been recently reported that the L and S variants of the promoter polymorphism modulate SLC6A4 differently. The S allele is associated with reduced transcription of SLC6A4 and consequently a reduction in serotonin reuptake 22. The investigations have revealed that 5-HTTLPR could be related to suicidal behaviors 24,27, depression 28, anger 29, and alcoholism 30. Several studies have evaluated the correlation between a variety of polymorphisms and aphthous lesions. None of them, however, has assessed 5-HTT gene polymorphism related to this disease among Iranian population while the 20.7% prevalence of RAS in Iran necessitates it to study various aspects of this issue.
Since psychological and genetic factors influence RAS pathogenesis, the aim of the present study was to evaluate 5-HTTLPR polymorphism in 5-HTT gene in patients with RAS in comparison to that in healthy subjects.

 

Materials and Methods :

Subjects: This case-control study was conducted on the patients attending the oral medicine department of the International Campus of Dental School, Tehran University of Medical Sciences. One hundred patients with RAS were selected as the case group and one hundred healthy subjects participated as the control group. Both groups were selected from Iranian population. The study process was approved by the Medical Ethics Committee, Office of Vice Chancellor for Research, Tehran University of Medical Sciences.
The inclusion criteria included presence of aphthous lesions which were examined and diagnosed by an oral medicine specialist in the department and recurring episodes of aphthous ulcers at least three times a year according to patient’s history. In this study, 50 male patients and 50 female patients participated.The exclusion criteria included presence of any local oral disease or systemic disorder with oral manifestations including Behcet’s syndrome, Celiac disease, AIDS, pregnancy and the use of immunomodulatory drugs, systemic steroids, or cytotoxic drugs during the last month.
The consent forms were then signed by the study participants or their parents (for the participants up to 18 years old).
A 5 ml blood sample was taken from each one of the study participants and was poured in a plastic test tube containing 300 µl of ethylene diaminetetraacetic acid (EDTA). The demographic data of the patients, the sampling date, and the sample number were registered on the tubes. The test tubes were then stored in a freezer at -20oC until DNA purification time.
DNA extraction from white blood cells: To extract DNA, 10 ml of cold distilled water was poured into each test tube containing frozen blood. The tubes were then placed on a tube rotator for 30 min to melt the frozen blood and make the Red Blood Cell (RBC) hemolysis possible.
All blood-contained tubes were then centrifuged at 4500 Relative Centrifugal Force (RCF) for 20 min until a red sediment was formed from destroyed RBCs and WBCs at the bottom of the tube. The liquid supernatant was then poured away. Thereafter, 5 ml of cold distilled water was poured into the test tube and the process mentioned above was performed for two more times.
Thereafter, Tris buffer 0.606 ml (10 mM), WB lysis, NaCl 11.688 g [400 mM], 0.372 g EDTA [2 mM], SDS (100 µl), and proteinase K (200 µl) were poured in to each tube and mixed together until the sediment was detached from the bottom of the tube and mixed with the small drop of proteinase k which was probably adhered to tube wall. The tubes were placed in bain-marie (55oC), on a shaker for 24 hr in order to separate strands of DNA. The test tubes were then centrifuged at 5500 RCF for 30 min, and the liquid supernatant was poured into other new tubes. Then, 5 ml of cold ethanol was poured into each tube and the white bundle of DNA was gradually formed.
The quality and quantity of the DNA obtained were measured using OD260/OD280 ratio. In this ratio value, 1.8 indicates DNA of high purity, and lower values indicate contamination by RNA 18.
PCR (Polymerase Chain Reaction): The selective replication from DNA fragments was performed in the presence of a proper buffered solution containing magnesium ions, proper primers, and Taq polymerase enzyme. PCR products were visualized by agarose gel electrophoresis. The gel was stained with ethidium bromide and the analyses were performed 18. 
DNA of the patients and healthy control subjects was extracted using a pair of primers capable of distinguishing S/L alleles and replicating 5-HTTLPR. An instance of PCR by primers is shown in figure 1.
The results of PCR process in case and control groups were then evaluated and all the subjects were divided into three genotype groups: heterozygote with two PCR bands for S and L alleles (LS), homozygote with one PCR band for S alleles (SS), and homozygote with one PCR band for L alleles (LL).
Gel electrophoresis stained with green viewer is shown in figure 2. The DNA size marker is available and the aphthous patient samples are shown in numbers 1 to 7. Numbers 1, 2, 4, and 6 show heterozygote for LS, number 3 shows homozygote for LL, and number 7 shows homozygote for SS.
Statistical analysis: The qualitative data of the present study were reported by crude and relative frequency. Chi-squared test, or Fisher's exact test (where necessary) served to compare the distribution of genotype and allele frequencies between two groups. Significance level was set at p<0.05. 
Logistic regression analysis served to compare 5-HTT allele and genotype frequencies between the two groups.

 

Results :

No statistically significant difference existed in the risk of RAS between the subjects with LL genotype and the subjects with LS genotype (p=0.98) (Table 1).
The SS genotype was associated with a 4.13 time higher risk of RAS as compared to the LL genotype, as given (Table 1) (p<0.001). Therefore, having S allele approximately doubled the risk of RAS (p<0.001).

 

Discussion :

RAS is not recognized as a single disease, but a clinical manifestation of several pathologic conditions such as hematologic and immunologic diseases, stress, and psychological disorders 7,9,10. 
In previous studies, the levels of depression, anger, and stress in the patients suffering from RAS were determined using Hamilton Anxiety Depression (HAD) scale 11, and the psychological factors were demonstrated to be highly associated with RAS pathogenesis 11-13. 
Approximately, 46% of the patients with RAS have a positive family history 15. Local trauma, iron deficiency anemia, folic acid deficiency, vitamin B12 resorption defect 16, neutropenia 17, and psychological factors such as stress and anger 13 can play a role in RAS etiology.
The 5-HTT gene modulates the intensity and duration of serotonergic neurotransmission, thus, this gene polymorphism can influence the anxiety related behaviors 24,25. It has been recently reported that the L and S variants of the promoter polymorphism modulate SLC6A4 differently. The S allele is associated with reduced transcription of SLC6A4 and consequently a reduction in serotonin reuptake 25. Several studies have evaluated the correlation between a variety of polymorphisms and aphthous lesions; however, none of them has assessed 5-HTT gene polymorphism related to this disease among Iranian population.
In the present study, 100 patients suffering from RAS and 100 healthy subjects were evaluated. The genotypes of 5-HTTLPR were divided into three groups by PCR using specific primers: homozygote for SS, homozygote for LL, and heterozygote for LS. L and S allele frequencies showed no statistically significant relation with RAS patients as compared to the healthy subjects. Totally, the results of the present study demonstrated that the frequency of 5-HTTLPR genotype and L/S alleles could be considered as a risk factor for RAS development and progression.
In 2005, Victoria et al evaluated the polymorphism of serotonin transporter gene in 69 patients suffering from RAS and 70 healthy subjects in Brazil. The results of their study showed a significant increase in incidence of SS genotype, S allele, and 5-HTTLPR polymorphism in the patients with RAS compared to the healthy subjects 21.
In 2004, researchers in Michigan University performed a systematic review on the relation between the polymorphism in the promoter region of the serotonin transporter gene (5-HTTLPR) and anxiety/ anger related behaviors. They evaluated 23 studies applying meta-analysis. The results revealed a significant relation between the polymorphism of 5-HTTLPR and neuroticism 31.
According to the results of our study, 5-HTTLPR genotypes and S/L allele frequencies seem to be associated with some of stress-related or auto-immune diseases among Iranian population.

 

Conclusion :

According to the results of our study, 5-HTTLPR genotypes and S/L allele frequencies seem to be associated with some of stress-related or auto-immune diseases among Iranian population.

 

Acknowledgement :

This research was supported by International Campus Tehran University of Medical Sciences. We thank our colleagues from International Campus Tehran University of Medical Sciences who provided insight and expertise that greatly assisted the research.

 



<p>Figure 1. An instance of PCR using primers.</p>

Figure 1. An instance of PCR using primers.


<p>Figure 2. Gel electrophoresis stained with green viewer.</p>

Figure 2. Gel electrophoresis stained with green viewer.


<p>Table 1. The frequency distribution and the relation between the genotype and 5-HTTLPR alleles, the case (n=100) and control (n=100) groups (29)</p>

Table 1. The frequency distribution and the relation between the genotype and 5-HTTLPR alleles, the case (n=100) and control (n=100) groups (29)


References :
  1. Messadi DV, Younai F. Aphthous ulcers. Dermatol Ther 2010;23(3):281-290.   [PubMed]
  2. Wilhelmsen NS, Weber R, Monteiro F, Kalil J, Miziara ID. Correlation between histocompatibility antigens and recurrent aphthous stomatitis in the Brazilian population. Braz J Otorhinolaryngol 2009;75(3):426-431.   [PubMed]
  3. Riera Matute G, Riera Alonso E. [Recurrent aphthous stomatitis in Rheumatology]. Reumatol Clin 2011;7(5):323-328. Spanish.   [PubMed]
  4. Safadi RA. Prevalence of recurrent aphthous ulceration in Jordanian dental patients. BMC Oral Health 2009;9:31.   [PubMed]
  5. Neville BW, Allen MA, Damm DD, Chi AC. Oral and maxillofacial pathology. 6th ed. Canada: Saunders/ Elsevier; 2008. 849 p.
  6. Momen-Beitollahi J, Mansourian A, Momen-Heravi F, Amanlou M, Obradov S, Sahebjamee M. Assessment of salivary and serum antioxidant status in patients with recurrent aphthous stomatitis. Med Oral Patol Oral Cir Bucal 2010;15(4):e557-561.   [PubMed]
  7. Jurge S, Kuffer R, Scully C, Porter SR. Mucosal disease series. Number VI. Recurrent aphthous stomatitis. Oral Dis 2006;12(1):1-21.   [PubMed]
  8. Bazrafshani MR, Hajeer AH, Ollier WE, Thornhill MH. Recurrent aphthous stomatitis and gene polymorphisms for the inflammatory markers TNF-alpha, TNF-beta and the vitamin D receptor: no association detected. Oral Dis 2002;8(6):303-307.   [PubMed]
  9. Bazrafshani MR, Hajeer AH, Ollier WE, Thornhill MH. IL-1B and IL-6 gene polymorphisms encode significant risk for the development of recurrent aphthous stomatitis (RAS). Genes Immun 2002;3(5):302-305.   [PubMed]
  10. Victória JM, Kalapothakis E, Silva Jde F, Gomez RS. Helicobacter pylori DNA in recurrent aphthous stomatitis. J Oral Pathol Med 2003;32(4):219-223.   [PubMed]
  11. McCartan BE, Lamey PJ, Wallace AM. Salivary cortisol and anxiety in recurrent aphthous stomatitis. J Oral Pathol Med 1996;25(7):357-359.   [PubMed]
  12. Antoon JW, Miller RL. Aphthous ulcers--a review of the literature on etiology, pathogenesis, diagnosis, and treatment. J Am Dent Assoc 1980;101(5):803-808.   [PubMed]
  13. Chiappelli F, Cajulis OS. Psychobiologic views on stress-related oral ulcers. Quintessence Int 2004;35(3):223-227.   [PubMed]
  14. Roitt IM, Leher T. Immunology of oral diseases. 1 st ed. USA: Blackwell Science Ltd; 1980. 464 p.
  15. Natah SS, Konttinen YT, Enattah NS, Ashammakhi N, Sharkey KA, Häyrinen-Immonen R. Recurrent aphthous ulcers today: a review of the growing knowledge. Int J Oral Maxillofac Surg 2004;33(3):221-234.   [PubMed]
  16. Altenburg A, Abdel-Naser MB, Seeber H, Abdallah M, Zouboulis CC. Practical aspects of management of recurrent aphthous stomatitis. J Eur Acad Dermatol Venereol 2007;21(8):1019-1026.   [PubMed]
  17. Thomas HC, Ferguson A, McLennan JG, Mason DK. Food antibodies in oral disease: a study of serum antibodies to food proteins in aphthous ulceration and other oral diseases. J Clin Pathol 1973;26(5):371-374.   [PubMed]
  18. Jaber L, Weinberger A, Klein T, Yaniv I, Mukamel M. Close association of HLA-B52 and HLA-B44 antigens in Israeli Arab adolescents with recurrent aphthous stomatitis. Arch Otolaryngol Head Neck Surg 2001;127(2):184-187.   [PubMed]
  19. Victoria JM, Correia-Silva Jde F, Pimenta FJ, Kalapothakis E, Gomez RS. Serotonin transporter gene polymorphism (5-HTTLPR) in patients with recurrent aphthous stomatitis. J Oral Pathol Med 2005;34(8):494-497.   [PubMed]
  20. Najafi S, Firooze Moqadam I, Mohammadzadeh M, Bidoki AZ, Yousefi H, Farhadi E, et al. Interleukin-10 gene polymorphisms in recurrent aphthous stomatitis. Immunol Invest 2014;43(4):405-409.   [PubMed]
  21. Scully C, Porter S. Oral mucosal disease: recurrent aphthous stomatitis. Br J Oral Maxillofac Surg 2008;46(3):198-206.   [PubMed]
  22. Gallo Cde B, Mimura MA, Sugaya NN. Psychological stress and recurrent aphthous stomatitis. Clinics (Sao Paulo) 2009;64(7):645-648.   [PubMed]
  23. Greenberg BD, Li Q, Lucas FR, Hu S, Sirota LA, Benjamin J, et al. Association between the serotonin transporter promoter polymorphism and personality traits in a primarily female population sample. Am J Med Genet 2000;96(2):202-216.   [PubMed]
  24. Lesch KP, Balling U, Gross J, Strauss K, Wolozin BL, Murphy DL, et al. Organization of the human serotonin transporter gene. J Neural Transm Gen Sect 1994;95(2):157-162.   [PubMed]
  25. Amanlou M, Babaee N, Saheb-Jamee M, Salehnia A, Farsam H, Tohidast Akrad Z. Efficacy of Satureja khuzistanica extract and its essential oil preparations in the management of recurrent aphthous stomatitis. DARU J Pharm Sci 2007;15(4):231-235.   [Abstract]
  26. Altenburg A, Zouboulis CC. Current concepts in the treatment of recurrent aphthous stomatitis. Skin Therapy Lett 2008;13(7):1-4.   [PubMed]
  27. Lesch KP, Bengel D, Heils A, Sabol SZ, Greenberg BD, Petri S, et al. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science 1996;274(5292):1527-1531.   [PubMed]
  28. Ramamoorthy S, Bauman AL, Moore KR, Han H, Yang-Feng T, Chang AS, et al. Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization. Proc Natl Acad Sci USA 1993;90(6):2542-2546.   [PubMed]
  29. Heils A, Teufel A, Petri S, Stober G, Riederer P, Bengel D, et al. Allelic variation of human serotonin transporter gene expression. J Neurochem 1996;66(6):2621-2624.
  30. Bellivier F, Szöke A, Henry C, Lacoste J, Bottos C, Nosten-Bertrand M, et al. Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders. Biol Psychiatry 2000;48(4):319-322.   [PubMed]
  31. Sen S, Burmeister M, Ghosh D. Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits. Am J Med Genet B Neuropsychiatr Genet 2004;127b(1):85-89.   [PubMed]