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  • The Internet Journal of Dental Science
  • Volume 5
  • Number 2

Original Article

Salivary t-PA level in Periodontitis: A Preliminary Report

B Rai, S Kharb, R Jain, S Anand

Keywords

periodontal disease, saliva, tissue plasminogen activator

Citation

B Rai, S Kharb, R Jain, S Anand. Salivary t-PA level in Periodontitis: A Preliminary Report. The Internet Journal of Dental Science. 2006 Volume 5 Number 2.

Abstract

Saliva is a diagnostic tool for many oral and systemic disease. Saliva samples were obtained from periodontitis patients and normal periodontal without any systemic disease were selected. The activities of t-PA tissue plasminogen activator activity were measured using in-house microtiter plate assays. The t-PA levels was higher in periodontitis as compared to normal periodontology subjects.

 

Introduction

Saliva is a diagnostic tool for many oral and systemic disease.1,2,3 Saliva being non-invasive and easy to collect can be used to early detection of oral diseases. Periodontal disease, a common chronic oral inflammatory disease, is characterized by destruction of soft tissue and bone surrounding the teeth. Tissue plasminogen activators (t-PA) level increased in periodontitis as compared to healthy periodontal.4 It is known that tissue plasminogen activator (t-PA) plays a key role in the lysis of blood clots.5 t-PA was shown to be physiologically active in human saliva6, and oral epithelial cells synthesized and released tPA in saliva. Hence, the present study was planned to detection of salivary t-PA in periodontitis patients.

Material and Methods

The twenty two (M:F 12:10 in age group 30-40 years) having atleast a minimum of seven sites exhibiting, 6 mm loss of clinical attachment who referred to Dept. of Periodontology. The patient had periodontitis characterized by a horizontal loss of supporting tissue by more than 1/3rd of root length with bleeding on probing, 4.3 mm average pocket depth, 7.6 mm average loss of attachment, and furcation involvements of the multi-rooted teeth.

The ten periodontal normal 5M, 5F (age 30-40 years) were selected as a control. During the examination, paraffin wax stimulated whole saliva was collected, and samples were stored at –4°C until analyzed. Saliva were centrifuged at 8000 g for a minutes, and level of t-PA in supernatant were determined using an immuno capture assay, as described previously.7 In none of participants was cardiovascular disease or any other ongoing general disease or infections diagnosed. Patients were excluded from the study if they had alcoholic or chronic smoker.

Data was analyzed by SPSS (version 7.0) and ‘t' student was applied.

Results

t-PA (IU/ml) level in various groups (mean ± SD)

Figure 1

t-PA levels is significantly higher in periodontitis as compared to normal (control) [Table I, p<0.01]

To our knowledge this is first study showing that t-PA level in periodontitis higher as compared to control. It has been recently observed that t-PA level in recurrent upper respiratory tract infections and with hyphyseal tumor higher.8 t-PA act as primary plasminogen activator in human saliva.9 Further studies are required on large samples to determine the relationship between t-PA level in saliva and oral infection.

References

1. Rai B, Jain R, Anand SC, Kharb S. 8-hydroxydeoxygenanosine levels: periodontitis in smoker and non-smoker: a pilot study. J Pak Dent Assoc 2006; 15 (2): 89-90.
2. Rai B, Kharb S, Jain R, Anand SC. Salivary lipid peroxidation product malonaldehyde in various dental diseases. World J Med Sci 2006; 1 (2): accepted.
3. Mandel ID. The role of saliva in maintaining oral homeostasis. JADA 1989; 119: 298-304.
4. Joshipura KJ, Wand HC, Merchant AT, Rimm EB. Periodontal disease and biomarkers related to cardiovascular disease. J Dent Res 2004; 83 (2): 151-55.
5. Collen D. On the regulation and control of fibronolysis. Edward Kowalski Memorial Lecture. Thromb Haemost 1980; 43: 77-79.
6. Sindet-Pederson S, Jesperson J. Characterization of plasminogen activators in unstimulated and stimulated human whole saliva. J Dent Res 1987; 66: 1199-1203.
7. Stephens RW, Leung KC, Pollanen J, Salonen EM, Vaheri A. Microplate immunocapture assay for plasminogen activators and their specific inhibitors. J Immunol Methods 1987; 105: 245-51.
8. Virtanen JO, Siren V, Multanen J, Farkkila M, Leive I, Vaheri A, Koskiniemi M. Plasminogen activators and their inhibitors in human saliva and salivary gland tissue. Eur J Oral Sci 2006; 114: 22-26.
9. Kjaeldgaard A, Kjaeldgaard M. Immunological characterization of plasminogen activators in human mixed saliva. Acta Physiol Scand 1986; 126: 443-447.

Author Information

Balwant Rai, B.D.S.
Resident, Government Dental College, Pt. Bhagwat Dayal Sharma, Post Graduate Institute of Medical Science

Simmi Kharb, M.D.
Bio-chemistry, Pt. Bhagwat Dayal Sharma, Post Graduate Institute of Medical Science

Rajnish Jain, M.D.S.
Endodontics, Pt. Bhagwat Dayal Sharma, Post Graduate Institute of Medical Science

S.C. Anand, M.D.S.
Oral & Maxillofacial Surgery and Orthodontics, Government Dental College, Pt. Bhagwat Dayal Sharma, Post Graduate Institute of Medical Science

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