Journal of Indian Society of Periodontology
Journal of Indian Society of Periodontology
 Home | About JISP | Search | Accepted articles | Current Issue | Archives | Instructions | Online submissionSubscribeLogin 
Users Online: 31  Home Print this page Email this page Small font size Default font size Increase font sizeWide layoutNarrow layoutFull screen layout


 
ORIGINAL ARTICLE
Year : 2008  |  Volume : 12  |  Issue : 2  |  Page : 41-44 Table of Contents   

Comparison of neutrophil functions in diabetic and healthy subjects with chronic generalized periodontitis


1 Department of Periodontics, MCODS, Mangalore., India
2 Department of Periodontics, ABSMIDS, Mangalore, India

Date of Submission17-Oct-2008
Date of Acceptance04-Nov-2008

Correspondence Address:
Neetha Shetty
Department of Periodontics, MCODS, Mangalore - 575 001.
India
Login to access the Email id


DOI: 10.4103/0972-124X.44089

PMID: 20142943

Get Permissions

   Abstract 

Background : Diabetes mellitus is a systemic condition that has long been associated with an increased risk and severity of periodontal disease. Polymorphonuclear leukocytes (PMNs) play a key role in the maintenance of gingival and periodontal health. Reduced PMN function has been found in patients with diabetes. Aim: The objective of this study was to evaluate PMN functions in 15 diabetic patients with chronic generalized periodontitis. Materials and Methods: Chemotaxis, superoxide production, phagocytosis and killing of Porphyromonas gingivalis by diabetic PMNs were evaluated relative to healthy and matched controls. Results: These analyses revealed a significant (P < 0.01) depression in the number of diabetic PMNs migrating along an fMLP gradient. In addition, a significant (P < 0.01) enhancement of diabetic PMN superoxide production was observed. Phagocytosis (P < 0.05) and killing by diabetic PMN of P. gingivalis was also impaired significantly (P < 0.01).

Keywords: Diabetes mellitus, periodontitis, polymorphonuclear leukocyte


How to cite this article:
Shetty N, Thomas B, Ramesh A. Comparison of neutrophil functions in diabetic and healthy subjects with chronic generalized periodontitis. J Indian Soc Periodontol 2008;12:41-4

How to cite this URL:
Shetty N, Thomas B, Ramesh A. Comparison of neutrophil functions in diabetic and healthy subjects with chronic generalized periodontitis. J Indian Soc Periodontol [serial online] 2008 [cited 2014 Sep 30];12:41-4. Available from: http://www.jisponline.com/text.asp?2008/12/2/41/44089


   Introduction Top


Diabetes mellitus (DM) is a major health problem in the world. Approximately 5% of diabetics are classified as type-1 (insulin dependent DM), a condition characterized by abrupt onset at any age, destruction of pancreatic islet cells, and dependence on exogenous insulin. The more prevalent form of diabetes is type-2 (noninsulin dependent DM), a condition which often develops over a period of time, involves reduced responsiveness of tissues to circulating insulin, and is often controlled by diet or oral hypoglycemic agents. Both types are characterized by hyperglycemia, hyperlipidemia, and associated complications. [1],[2]

Among the systemic factors, the relationship between periodontal disease and DM has been studied extensively. Many investigators, in their epidemiological, experimental, and clinical studies have reported that the severity of periodontal disease is significantly greater among diabetics than in nondiabetics. [3],[4],[5],[6],[7],[8]

Numerous studies have identified a clear role of PMN's in the maintenance of gingival and periodontal health. Reduced PMN function has been found in patients with diabetes. PMN dysfunction studies in diabetics have exhibited defects in chemotaxis, phagocytosis and killing, and increased release of super oxide. [9]

Diabetic patients with chronic periodontitis have depressed chemotaxis compared with nondiabetic patients with chronic periodontitis. Neutrophils from periodontitis patients generate abnormally high levels of oxygen radicals in response to stimuli. This is an important bactericidal mechanism, but the same mechanism has the potential to induce tissue destruction. In diabetic patients with periodontitis, super oxide release is enhanced due to both hyperglycemic state and periodontitis condition which brings about pronounced tissue destruction when compared to healthy subjects with periodontitis. [10],[11]

Hence, in the present study, an attempt is made to assess the influence of DM on the neutrophil functions as estimated by chemotaxis, phagocytosis and killing, and super oxide release; and to evaluate the possible correlation of the severity of periodontal disease and neutrophil abnormalities in diabetics and nondiabetics.


   Material and Methods Top


The subjects for this study were selected from the OPD, Department of Periodontitics, ABSMIDS, and from the diabetic clinic of KSHEMA hospital, Deralakatte, Mangalore.

The study comprised of 60 subjects, inclusive of both sexes, who were in the age group of 30-60 years and were divided into two groups of 30 diabetics and 30 nondiabetics with chronic periodontitis.

Inclusion criteria

  1. Number of teeth present - 20.
  2. Number of sites involved should have ≥2 mm clinical attachment loss with presence of disease activity as recorded by gingival index (Loe and Silness).


Exclusion criteria

  1. History of any systemic disease for the control group.
  2. History of any systemic disease other than diabetes for the test group.
  3. Brittle diabetics.
  4. Pregnant women and lactating mothers.
  5. Presence of any habits like smoking and alcoholism.
  6. History of antibiotic therapy within 6 months prior to study.


A standard profoma consisting of the following data: name, age, sex, medical and past dental history, plaque index (Silness and Loe), gingival index (Loe and Sillness), and clinical attachment for each patient were recorded. Each patient was examined using a mouth mirror and William's graduated periodontal probe under artificial light.

Neutrophil function tests

The tests include chemotaxis, phagocytosis and killing, and super oxide estimation. [12] Five milliliters of venous blood was drawn from the antecubital vein with a needle and a disposable syringe; 2.5 ml of this blood was transferred into a plain vial (for phagocytosis), and the remaining 2.5ml into the vial containing EDTA and transported to the laboratory.

Preparation of cells

After doing a total count and differential count of WBCs to confirm their presence in normal range, the blood in the plain vial was incubated at 37°C for 2 hours and the serum was separated for use in the phagocytic study. The blood collected in the vials with EDTA were mixed with equal quantities of RPMI 1640 and one-third volume of 6% dextran and kept at room temperature for 1 hour. Supernatant was collected in test tubes and washed 3-4 times with RPMI to remove traces of plasma and dextran and cells were maintained in RPMI 1640 medium. [13]

Neutrophil chemotaxis

The cells were prepared in RPMI 1640 solution and the neutrophils adjusted at 5 X 10 6 /ml, making sure that the cell concentration was same in the test and control samples. The lower compartment of the chemotactic chamber was filled with FMLP as the chemotactic factor (FMLP/mg/ml in Hanks balanced salt solution).

The upper compartment was filled with cell suspension and placed inside the lower compartment, and the chamber was incubated at 37ºC in air for 3 hours. At the end of 3 hours, the test was taken out of the incubator and the upper compartment was removed and emptied. The upper compartment was then immersed in 70% ethanol or methanol for a few minutes so that the glue melted and the filter became loose from the bottom of the syringe. This was picked up with a tweezer, taking care not to touch the rim and stain it.

Once fixed, it was mounted under a cover slip with the lower side of the filter facing up and examined for the presence of neutrophils that have crossed to the lower surface of the filter. [14],[15]

Phagocytosis of P. gingivalis

Preparation of P. gingivalis

Commercially available P. gingivalis in blood agar was grown in schaedlers broth at 37ºC, 48 hours prior to phagocytosis. [16] The cultures were spun at 1500 g for 10 minutes in a centrifuge. The deposits were washed twice with phosphate buffer saline and filtered twice through sterile gauze and resuspended in Hanks balanced salt solution at 5 x 10 7 CFU/ml.

Method

The contents of the tube were mixed and incubated at 37ºC for 30 minutes. It was then centrifuged at 200 g for 5 minutes and the supernatant removed with Pasteur pipette leaving a droplet into which the sediment was resuspended. Smears were made, air dried, and stained with giemsa. At least 200 neutrophils were examined. A count of the number of ingested P. gingivalis associated with each cell was made.

Bactericidal assay

To the above-mentioned contents, 4 ml of 0.01% methylene blue was added and centrifuged at 1500 g at 4ºC for 10 minutes. [17] The supernatant was removed with Pasteur pipette leaving a droplet to resuspend the organisms. The suspension was incubated in an ice bath until ready for counting. Counting was done within 3 hours with a Neubaeurs chamber. At least 200 PMNL's/slide were counted. Dead bacteria appeared blue.

Super oxide estimation

The solution was taken in a 10 ml beaker and illuminated for 10 minutes by keeping the beaker in an aluminium-foil-lined box fitted with a 15 W fluorescent lamp. Then the absorbance was read at 560 nm. One unit of super oxide activity was taken as that producing 50% inhibition of NBT reduction. The values obtained were subjected to statistical analysis. The test of significance applied was student unpaired t test.


   Results Top


When the periodontal status of the diabetic group was compared with the healthy group, the amount of local factors and periodontal destruction was more in the healthy group, but some patients with diabetes showed comparatively more destruction than expected with lesser plaque scores.

The results of the present study also demonstrated that diabetic patients had defects in neutrophil functions when compared to healthy subjects as measured by chemotaxis, phagocytosis, microbicidal function, and super oxide released.

[Table 1] compares the mean and standard deviation of chemotaxis of neutrophil between the two groups and it was seen that the diabetic group showed defective chemotaxis with a mean of 18.733 + 5.663 and a mean of 30.667 + 4.909 for the control group which was highly significant with the P value of 0.01.

[Table 2] compares the mean and standard deviation of phagocytosis of P. gingivalis as evaluated by mean particle number (MPN). It was seen that the MPN was significant in the healthy group with a mean of 3.600 + 1.957 and a mean of 1.533 + 0 .743 for the diabetic group with the P value of 0.05.

[Table 3] assesses the intracellular killing capacity of neutrophils. It was revealed that the diabetic neutrophils had definitive low intracellular microbicidal function with a mean of 5.733 + 2.987 for the diabetic group and a mean of 12.600 + 8.798 for the control group with the P value of 0.01 which was again highly significant when compared to healthy subjects.

[Table 4] assesses the super oxide released by the neutrophils of the two groups as estimated by the activity of super-oxide dismutase. It was again seen that the super oxide released by the diabetic neutrophils was higher with a mean of 108.400 + 15.697 when compared to the healthy neutrophils, which had a mean of 24.133 + 14.212, as estimated by the intensity of the solution was more, which was very highly significant with the P value of 0.001.


   Discussion Top


The probable influence of DM on the onset and duration of periodontal disease has been studied for many years. On the basis of experimental and clinical investigations, it is generally accepted that diabetes may result in a greater severity of periodontal disease. The mechanism of increased susceptibility to periodontitis in diabetics is not entirely clear.

According to a few investigators, the primary factor responsible for the development of diabetic complications is prolonged tissue response to hyperglycemia, which results in the production of advanced glycated end products. Also, there may be an increase in the local production of cytokines leading to connective tissue damage, bone resorption, and delayed wound repair. [1],[18],[19]

Several studies in diabetic animals and humans have reported defects in neutrophil functions, namely chemotaxis, phagocytosis, killing and microbicidal function, and super oxide released, which could be one of the reasons for increased susceptibility to periodontitis in these subjects. [2],[9],[20],[21]

In the present study, two groups of subjects, 30 diabetics with periodontitis and 30 healthy individuals with periodontitis were compared for their periodontal status which included plaque index, gingival index, and attachment level, and neutrophil functions that included chemotaxis, phagocytosis of P. gingivalis , killing and microbicide of P. gingivalis , and amount of super oxide released.

When the periodontal status of healthy subjects with periodontitis was compared with that of the diabetic subjects with periodontitis, the amount of local factors and periodontal destruction was more in the healthy subjects, but some in the diabetic group showed comparatively more destruction than expected with lesser plaque scores. The mean plaque score was significantly less in the diabetic group than the healthy group with periodontitis who were age matched. This finding in our study is in agreement with Cohen et al . [7] who reported a significantly less plaque score in diabetics.

In the present study, in general, age of the patient and amount of local factors played an important role on periodontal status, and this is in agreement with studies done by Belting et al .[18]

Several investigators have stated that increased periodontitis is not detected in diabetic patients with plaque-free dentition, suggesting the presence and amount of local deposits is directly related to periodontal breakdown due to diminished host resistance. [22]

The results of the present study demonstrated that the diabetic patients with periodontitis had defects in neutrophil functions when compared to the healthy subjects with periodontitis. When chemotaxis was compared between the groups, defective chemotaxis was seen in the diabetic group, which is in agreement with the study done by Mowat and Baum [21] who showed significantly less chemotaxis with DM. They suggested that this defect in chemotaxis of diabetic leukocytes could contribute increased infections in these patients.

When phagocytosis of P. gingivalis was evaluated by MPN, that is the number of P. gingivalis phagocytosed by the neutrophils, it was seen that MPN was significantly higher in healthy subjects than the diabetic group. This result of our study is in agreement with the studies of Bybee et al [16] and Martha Walter et al , [23] who have reported impaired phagocytosis in diabetic individuals. In the present study, we used P. gingivalis as a model organism because it is one of the primary pathogens causing periodontitis.

When intracellular killing capacity of the neutrophils was assayed, it was seen that the diabetic PMNL's had a definite low intracellular microbicidal function. This abnormality was not only pronounced in diabetics but was also present to some extent in healthy subjects with periodontitis. This finding is in agreement with the study by Giovanni Salvi et al . [24] who stated that the local polysaccharides may alter oxidative burst capacity to impair killing.

When super oxide released was assayed using super oxide dismutase enzyme in the presence of nitroblue tetrazolium, it was found that the intensity of the blue color was more in diabetic samples than the healthy group. This suggested that more super oxide dismutase enzyme was required in the diabetic group to scavenge the free oxygen radicals. This result is in agreement with Martha Walters et al. [23] who found that the super oxide released by diabetic neutrophils was more than the healthy subjects with periodontitis.

In conclusion, when the neutrophil functions between diabetic patients and healthy subjects were compared, it was found that:

  • Impaired neutrophil chemotaxis was observed in diabetic patients.
  • Defective phagocytosis of P. gingivalis by neutrophils was observed in diabetic patients.
  • The intracellular killing capacity of neutrophils was reduced in diabetic patients.
  • The super oxide released by diabetic PMN's was drastically increased.


These above defects in the neutrophils of diabetic patients could be a possible mechanism to render them more susceptible to periodontal diseases.

 
   References Top

1.Bjelland S, Bray P, Hirsch R. Dentists, diabetes and periodontitis. Aust Dent J 2002;47:202-7.  Back to cited text no. 1    
2.Cowie CC, Eberhardt MS. American diabetes association vital statistics. Am Diabetes Assoc 1996;20:13-20.  Back to cited text no. 2    
3.Barnett ML, Baker RL, Yancey JM, MacMillan DR, Kotoyan M. Absence of periodontitis in a population of insulin dependent diabetes mellitus patients. J Periodontol 1984;55:402-5.  Back to cited text no. 3  [PUBMED]  
4.Bartolucci EG, Parkes RB. Accelerated periodontal breakdown in uncontrolled diabetes: Pathogenesis and treatment. Oral Surg Oral Med Oral Pathol 1981;52:387-90.  Back to cited text no. 4  [PUBMED]  
5.Bay I, Ainamo J, Gad G. The response of young diabetics to periodontal treatment. J Periodontol 1974;45:806-8.  Back to cited text no. 5    
6.Belce A, Uslu E, Kucur M, Umut M, Ipbüker A, Seymen HO. Evaluation of salivary sialic acid level and Cu-Zn super oxide dismutase activity in type-1 diabetes mellitus. J Exp Med 2000;192:219-25.  Back to cited text no. 6    
7.Listgarten MA, Ricker FH Jr, Laster L, Shapiro J, Cohen DW. Vascular basement thickening in the normal and inflamed gingival of diabetics and non-diabetics. J Periodontol 1974;45:676-84.   Back to cited text no. 7  [PUBMED]  
8.Little JW, Falace DA, Miller CS, Rhodes NL. Dental management of the medically compromised patients. 5 th ed. 1997. p. 387-409.  Back to cited text no. 8    
9.Golub LM, Nicoll GA, Iacono VJ, Ramamurthy NS. In vivo crevicular leukocyte response to a chemotactic challenge: Inhibition by experimental diabetes. Infect Immun 1982;37:1013-20.  Back to cited text no. 9    
10.Haber J, Wattles Crowley R, Mandell R, Joshipura K, Kent R. Assessment of diabetes as a risk factor for periodontitis. J Dent Res 1991;70:414-5.   Back to cited text no. 10    
11.Hart TC, Shapira L, Van Dyke TE. Neutrophil defects as risk factors for periodontal disease. J Periodontol 1994;65:521-9.  Back to cited text no. 11    
12.Metcalf JA, Gallin JI, Nauseef WM, Root KR. Laboratory manual of neutrophil function. New York Press; 1986. p. 112.  Back to cited text no. 12    
13.Kalmar JR, Arnold RR, Narbington ML, Gardner MK. Superior leukocyte separation with a discontinuous one step Ficoll Hypaque gradient for isolation of human neutrophils. J Immunol Met 1988;110:275-81.  Back to cited text no. 13    
14.Oshrain HI, Telsey B, Mandel ID. Neutrophil chemotaxis in refractory cases of periodontitis. J Clin Periodontal 1987;14:52-5.  Back to cited text no. 14    
15.Van Dyke TE, Reilly AA, Horoszewicz H, Gagliardi N, Genco RJ. A rapid semi-automated procedure for the evaluation of leukocyte locomotion in the micropore filter assay. J Immunol Methods 1979;31:271-82.  Back to cited text no. 15    
16.Bybee JD, Rogers DE. The phagocytic activity of polymorphonuclear leukocytes obtained from patients with diabetes mellitus. J Lab Clin Med 1964;64:1-13.  Back to cited text no. 16    
17.Lawrence J. Emrich Mare Shlossman Robert J. Genco. Periodontal diseases in non- insulin dependent diabetes mellitus. J Periodontol 1991;62:123-30.  Back to cited text no. 17    
18.Belting CM, Himker JJ, Dummet CO. Influence of diabetes mellitus on the severity of periodontal disease. J Periodontol 1964;35:476-8.  Back to cited text no. 18    
19.Ainamo J, Lahtiren A, Uitto VJ. Rapid periodontal destruction in adult patients with poorly controlled diabetes. J Clin Periodontal 1990;17:22-8.  Back to cited text no. 19    
20.Grossi SG, Genco RJ. Periodontal disease and diabetes mellitus: A two-way relationship. Ann Periodontol 1998;3:51-61.  Back to cited text no. 20    
21.Alastair G, Mowat MB, Baum J. Chemotaxis of polymorphomuclear leucocytes from patients with diabetes mellitus. N Engl J Med 1971;284:12.  Back to cited text no. 21    
22.National diabetes data group. Diabetes in America; 1985.  Back to cited text no. 22    
23.Walters MI, Lessler MA, Stevenson TD. Oxidative metabolism of leukocytes from non-diabetic and diabetic patients. J Lab Clin Med 1971;78:158-66.  Back to cited text no. 23    
24.Giovanni E Salvi, Gaudie WM. Influences on periodontal disease: Nutritional and hormonal factors. J NZ Soc Periodontol 1998;67:7-14.  Back to cited text no. 24    



 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]


This article has been cited by
1 Targeting neutrophils in sepsis
Fabiane Sônego,José Carlos Alves-Filho,Fernando Queiróz Cunha
Expert Review of Clinical Immunology. 2014; : 1
[Pubmed]
2 High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
Anelise M Bosco,Breno FM de Almeida,Priscila P Pereira,Luis G Narciso,Valéria MF Lima,Paulo C Ciarlini
BMC Veterinary Research. 2013; 9(1): 24
[Pubmed]
3 Periodontitis and risk of diabetes mellitus : Periodontitis and risk of diabetes
Abhijit GURAV, Varsha JADHAV
Journal of Diabetes. 2011; 3(1): 21
[VIEW]
4 Deep neck abscesses: the Singapore experience
Yan Qing Lee, Jeevendra Kanagalingam
European Archives of Oto-Rhino-Laryngology. 2011; 268(4): 609
[VIEW]



 

Top
 
  Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
    Introduction
    Material and Methods
    Results
    Discussion
    References
    Article Tables

 Article Access Statistics
    Viewed1792    
    Printed130    
    Emailed1    
    PDF Downloaded527    
    Comments [Add]    
    Cited by others 4    

Recommend this journal