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|Year : 2020 | Volume
| Issue : 3 | Page : 575
Evaluation of Hematological profile in Oral Submucous Fibrosis: A Cross-sectional Study
Deepa Jatti Patil1, Manjiri Joshi2
1 Department of Oral Medicine and Radiology, KM Shah Dental College and Hospital, Sumandeep Vidyapeeth Deemed to be University, Piparia, Gujarat, India
2 Department of Oral Medicine and Radiology, Manubhai Patel Dental College, Hospital and Oral Research Institute, Vadodara, Gujarat, India
|Date of Submission||12-Feb-2020|
|Date of Decision||17-Aug-2020|
|Date of Acceptance||04-Sep-2020|
|Date of Web Publication||09-Jan-2021|
Deepa Jatti Patil
Department of Oral Medicine and Radiology, KM Shah Dental College and Hospital, Sumandeep Vidyapeeth Deemed to be University, Piparia, Vadodara - 391 760, Gujarat
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Aims: The purpose of this study was to estimate hemoglobin (Hb) level, red cell indices (RCIs), serum iron level and Vitamin B12 level in patients with oral submucous fibrosis (OSMF) and to analyze the association of these parameters in different stages of OSMF.
Setting and Design: This case–control study comprised of 65 individuals, with 40 OSMF patients and 25 controls. The OSMF patients were graded clinically according to the classification by Arakeri et al. Fasting blood samples were collected from both groups for hematological evaluation.
Statistical Analysis Used: The mean values and standard deviations were calculated by Chi-square test. Normality of various parameters was evaluated by Kolmogorov–Smirnov test. The independent t-test was used to compare more than two means simultaneously. Correlation analysis was done by Karl Pearson's correlation coefficient method.
Results: The OSMF patients were in the age range of 21–67 years, with a mean age of 39.85 ± 10.42 years. The mean value of Hb of the control group was 14.24 ± 1.03 g/dL, whereas that of OSMF group was 11.18 ± 2.06 g/dL (P < 0.001). The mean value of the serum iron level of the control group was 119.67 ± 42.42 μg/dL, whereas that of the OSMF group was 45.04 ± 10.41 μg/dL (P < 0.001). The mean value of serum Vitamin B12 levels of the control group was 422.98 ± 112.57 μg/dL, whereas that of the OSMF group was 211.78 ± 45.17 μg/dL (P < 0.001). The RCIs including packed cell volume, mean corpuscular volume, mean corpuscular Hb (MCH) and MCH concentration were significantly reduced in OSMF cases. Iron deficiency was present in 38 patients among the study group and Vitamin B12 deficiency was present in 22 patients of the study group.
Conclusion: OSMF causes depletion of minerals and trace elements, and its replenishment is required for the healing of tissues and performing daily routine activities.
Keywords: Chemoprevention, iron deficiency, oral submucous fibrosis, Vitamin B12 deficiency
|How to cite this article:|
Patil DJ, Joshi M. Evaluation of Hematological profile in Oral Submucous Fibrosis: A Cross-sectional Study. J Oral Maxillofac Pathol 2020;24:575
|How to cite this URL:|
Patil DJ, Joshi M. Evaluation of Hematological profile in Oral Submucous Fibrosis: A Cross-sectional Study. J Oral Maxillofac Pathol [serial online] 2020 [cited 2021 Jan 17];24:575. Available from: https://www.jomfp.in/text.asp?2020/24/3/575/306674
| Introduction|| |
Since 1950, oral submucous fibrosis (OSMF) has emerged as one of the most prevalent potentially malignant disorders (PMDs), largely among the people of Asian origin. The disease is mainly seen in India, Bangladesh, Sri Lanka, Pakistan, Taiwan, Southern China, Polynesia and Micronesia. About 2.5 million individuals are affected worldwide. The most common etiological factor hypothesized to initiate the condition is areca nut chewing, and nutritional deficiencies, immunologic processes and genetic predisposition are other associated factors.,
The condition is progressive, and patients present with varied clinical presentation depending on the stage of the disease at the time of diagnosis. The most common presentations include intolerance to spicy food and rigidity of lip, tongue and palate leading to decreased mouth opening; restricted tongue movements; dysphagia and hearing impairment in the advanced stages. The trademark of the disease is submucosal fibrosis involving most parts of the oral cavity, pharynx and upper third of the esophagus.
The role of nutritional deficiencies, principally of iron and vitamins, has been proposed in the etiology of OSMF. Significant research has been carried out to emphasize their role in OSMF. Wahi et al. reported a significantly higher prevalence of malnutrition in 104 OSMF patients than in 200 normal control participants. Iron has been studied as a diagnostic and prognostic marker in malignancies such as esophageal cancers (Plummer–Vinson syndrome) and postcricoidal carcinoma. Serum levels of iron were found to be significantly altered in oral cancer and PMDs. Vitamin B12 deficiency can cause moderate-to-severe epithelial dysplasia that resolves after correction of the deficiency. Both the trace elements are required for maintaining the integrity of the oral mucosa.,
There is paucity of literature regarding the role of Vitamin B12 and iron in OSMF. There is a need to assess whether these trace elements alter the course and progression of OSMF. Considering the multifactorial etiology, more research is required in this direction to develop sensitive, specific and faster tests in the diagnosis and prognosis of OSMF. Therefore, the study was conducted to estimate hematological parameters in OSMF patients and to analyze the association of the levels of serum iron, hemoglobin (Hb) and Vitamin B12 in different stages of OSMF.
| Subjects and Methods|| |
This cross-sectional study was designed after obtaining permission from the institutional ethical committee (IEC/MPDC_152/OD-11/18). The study population were selected from patients presenting for routine dental treatment with signs and symptoms of OSMF visiting the Department of Oral Medicine and Radiology, Manu Bhai Patel Dental College, Vadodara, Gujarat, India, from October 2018 to June 2019. Age- and gender-matched healthy controls were selected from patients who are free from systemic diseases and reporting for routine hematological investigations. Written informed consent was taken from all the study participants. The sample size was calculated using quantitative data by Ganapathy et al.
| Inclusion criteria|| |
The study population was divided into the following two Inclusion criteria-groups:
- Group I – Forty individuals with clinical diagnosis of OSMF above 18 years of age according to the diagnostic criteria by Arakeri Thomas et al.
- Group II – Twenty-five age- and gender-matched healthy controls, free of systemic diseases, with no oral lesions and no history of tobacco or areca nut chewing or alcohol intake.
Patients with stage IV OSMF, Oral mucosal lesions other than OSMF observed clinically; previously treated cases of OSMF; patients with oral mucosal lesions, systemic disorders such as diabetes, hypertension and liver/kidney disorders and/or those under treatment for any other systemic diseases were excluded from the study. In the control group, patients with pregnancy, those with a history of tobacco and areca nut chewing or alcohol intake, patients on iron and Vitamin B12 supplements in the last 6 months and patients unwilling to participate in the study were also excluded from the study.
All the patients fulfilling the inclusion criteria were informed about the study in their own mother tongue and only those who agreed to give a written signed voluntary consent were enrolled in the study. All the enrolled participants were interviewed and examined in the dental clinic using clinical examination tools after recording case history. During the interview, details of deleterious habits were also noted. After satisfying the diagnostic criteria of OSMF by Arakeri Thomas et al., the patients were recalled the next day early in the morning. The fasting blood sample was collected. Approximately 5 mL of venous blood was obtained by venipuncture of the median cubital vein after taking all aseptic precautions.
Estimation of iron, hemoglobin and red cell indices
Estimation of iron was done using Ferrene's method. The red cell indices (RCIs) and Hb level were analyzed by? the automated cell counter method. All the test tubes used for analysis were immersed overnight in deionized water and then washed the next day using deionized water. The serum sample used for the estimation was mixed with appropriate proportions of buffer and color reagents supplied in the iron estimation kit in clean, dry test tube as per the manufacturer's instructions. The absorbance of these samples was compared to that of the standard solution provided in the kits at 578 nm in a semi-autoanalyzer (Microlab – 200). Bucheon-si;Gyeonggi-do :South Korea.
Estimation of Vitamin B12 was done by the chemiluminescent microparticle intrinsic factor assay for the quantitative determination of Vitamin B12 in human serum method.
Statistical procedure was carried out using the IBM SPSS Statistics for Windows, version XX (IBM Corp., Armonk, N.Y., USA)'. The mean values and standard deviations for all the groups were calculated by Chi-square test. Normality of various parameters in the control and study groups was assessed by Kolmogorov–Smirnov test. Independent t-test was used to compare more than two means simultaneously, that is, whether there was a significant difference between the mean values of serum iron, Vitamin B12 and Hb among the two groups. Correlation analysis among various parameters in the control and study groups was done by Karl Pearson's correlation coefficient method. A logistic regression analysis was performed to predict which hematological variable was more significant for OSMF. The level of significance was fixed at P < 0.05.
| Results|| |
A total of sixty patients were evaluated for hematological investigations (32 males and 33 females). The study and the control group comprised 40 and 25 individuals, respectively. The OSMF group showed a slight female predominance with 22 females and 18 males. [Table 1] shows the gender distribution in the OSMF and control groups. The OSMF patients were in the age range of 21–67 years with a mean age of 39.85 ± 10.42 years. Comparison of the two study groups for age (control and study) by Chi-square test revealed the presence of majority of cases between 31 and 40 years and was statistically significant (P = 0.0111) [Figure 1]. The mean age of the control group was 31.00 ± 10.85 years.
|Table 1: Distribution of male and females in the control and study groups|
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[Figure 2] shows the distribution of OSMF patients according to the classification of Arakeri Thomas et al. [Table 2] shows the comparison of mean values of the hematological parameters in the study and control groups by independent t-test, and the values were statistically significant (P < 0.0001).
|Figure 2: Patient distribution in various grades of oral submucous fibrosis|
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The mean value of Hb of the control group was 14.24 ± 1.03 g/dL, whereas that of the OSMF group was 11.18 ± 2.06 g/dL (P < 0.001). The mean value of serum iron level of the control group was 119.67 ± 42.42 μg/dL, whereas that of OSMF group was 45.04 ± 10.41 μg/dL (P < 0.001). The mean value of serum Vitamin B12 levels of the control group was 422.98 ± 112.57 μg/dL, whereas that of OSMF group was 211.78 ± 45.17 μg/dL (P < 0.001).
[Figure 3] depicts the comparison of hematological parameters in the study and control groups. On analyzing the values by Pearson's correlations, it was observed that the values of Hb, packed cell volume, mean corpuscular volume, mean corpuscular Hb (MCH) and MCHC levels had a significant correlation with serum iron levels in the OSMF Stage III (correlation value: 0.6870, 0.6220, 0.6200, 0.4490 and 0.2110, respectively) [Table 3].
|Table 3: Correlation analysis among hematological parameters in the study group by Karl Pearson's correlation coefficient method|
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|Figure 3: Comparison of hematological parameters in the study and control groups|
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[Table 4] depicts the logistic regression analysis. Iron deficiency was present in 38 patients among the study group as compared to 3 patients in the control group. Odds ratio (OR) was 27.36, predicting the high occurrence of iron deficiency 27.36 times than the control group. Vitamin B12 deficiency was present in 21 patients in the study group as compared to 1 patient in the control group, with the OR of 3.91, predicting the occurrence of Vitamin B12 deficiency 3.91 times than that of the control group.
|Table 4: Logistic regression analysis of the study group by haematological parameters|
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The mean maximum mouth opening of the forty OSMF patients was 14.1. The soft palate, retromolar area and buccal mucosa were the three sites involved by OSMF in every patient, with extra involvement of labial mucosa in 19 patients (60.3%), floor of the mouth in 5 patients (48.5%) and tongue in 8 patients (39.7%). Of the 40 OSMF patients, 17 had three-site involvement, 18 had four-site involvement, 9 had five-site involvement and 5 had six-site involvement by OSMF.
| Discussion|| |
More and Rao proposed a new definition for OSMF based on extensive clinical research as a debilitating, progressive, irreversible collagen metabolic disorder induced by chronic chewing of areca nut and its commercial preparations; affecting the oral mucosa and occasionally the pharynx and oesophagus; leading to mucosal stiffness and functional morbidity; and has a potential risk of malignant transformation. Our study involving forty OSMF patients showed that 74.29% were gutkha users, 5.44% were pan users and only 21.11% were areca nut users, which was in concordance with studies carried out by Ranganathan et al. (69%) and a review by Murti et al. (98%). The prevalence of increased gutkha chewing over areca nut could be due to the easy availability of attractive, tiny, multicolored gutkha packets.
OSMF manifests early in gutkha chewers than betel quid chewers due to the presence of higher amount of dry weight tobacco content and absence of betel leaf (has beta carotene which acts as an antioxidant)., Areca nut induces mechanical abrasion, cytotoxicity and collagen cross-linking of the oral mucosa. The addition of nicotine amplifies the cytotoxicity induced by nicotine, leading to the production of damaged collagen.
The trismus, fibrosis and malignant classification by Arakeri Thomas et al. et al. was used in the present study as it helps in classifying the information efficiently, recording the data, proper communication, obtaining prognostic information and also to make it easy to understand the disease characteristics, which can be easily applied by the trainees and clinicians. It is a three-tier staging system, differentiating between medical, surgical and malignant disease therapy.
The present study shows decreased levels of serum iron, Hb and Vitamin B12 in OSMF patients as compared to the controls. Similar results were found in other studies conducted worldwide.,,,,,,,,, [Table 5] summarizes the studies conducted by various authors investigating the role of trace elements in OSMF. According to Wang et al., the levels of folic acid and Vitamin B12 had decreased in OSMF patients. Wahi et al. also found decreased Vitamin B12 and Vitamin C levels in OSMF group. Apart from these two studies, the present study assessed the prevalence of Vitamin B12 and RCIs in addition to other hematological parameters. The RCIs were not assessed in other studies.
|Table 5: Comparison of studies by various authors depicting the role of trace elements in oral submucous fibrosis|
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Ramanathan in his study reported that 10 (77%) of the 13 OSMF patients have iron deficiency anemia (IDA). The present study showed a significantly greater frequency of IDA in 37 OSMF patients (92.5%) than that in healthy control patients. Some studies have shown contrasting results. Wahi et al. discovered that 6% of the seventy male OSMF patients and 11% of the 34 female OSMF patients had anemia, but the frequency of anemia in OSMF patients did not differ significantly from that of the controls.
A study conducted by Bhardwaj et al. on 120 participants showed a progressive decline in serum iron and Hb levels from Stage I OSMF to Stage IV OSMF, which was also observed in the present study. The results obtained in our study are in accordance to the studies conducted by Ganapathy et al., Karthik et al., Lavina et al. et al. and Rupak et al.
Iron is the key element in the human body with important functions in DNA, RNA and collagen and involves in antibody synthesis apart from the regulation of numerous physiological and metabolic processes. It plays a vital role in the development and maintenance of oral mucosa.
IDA due to low serum iron levels manifests clinically as fatigue, achlorhydria, atrophy of epithelium, loss of attention, irritability, dyspnea and lowered memory. The oral manifestations include angular cheilitis, atrophic glossitis, generalized oral mucosal atrophy, candida infections, pallor and stomatitis. Plummer–Vinson syndrome or Paterson–Kelly syndrome or sideropenic dysphagia is a rare premalignant condition characterized by IDA, dysphagia and koilonychia, with women being affected more than men. Dysphagia results from the presence of abnormal esophageal webs which have predisposition toward malignant transformation.,
The hallmark histopathological features in OSMF are epithelial atrophy, dense corium and increased collagen production. The hypothesis of decreased iron levels in OSMF can be attributed to the following reasons. Cytochrome oxidase is required for the normal maturation of epithelium. In cases of IDA, it causes epithelial atrophy, making the mucosa vulnerable to irritants. OSMF is basically a disorder of collagen metabolic disorder due to overproduction of highly cross-linked insoluble collagen Type I. The hydroxylation reaction of collagen requires ferrous iron and ascorbic acid. Utilization of iron for the hydroxylation of proline and lysine, leads to decreased serum iron levels.
Lack of iron in tissues causes improper vascular channel formation, resulting in decreased vascularity. This leads to derangement in the inflammatory reparative response of the lamina propria, resulting in defective healing and scar formation, further augmenting the fibrosis.
Majority of the literature suggests that OSMF leads to iron deficiency due to impaired dietary habits, burning sensation, vesiculation and ulceration of the oral mucosa, causing difficulty in the consumption of normal diet, leading to poor nutrition. Bhattacharya et al. reported an interesting case where IDA primarily resulted in the development of OSMF, which was successfully treated by oral administration of iron supplements and antioxidants.
The key features of OSMF including chronic inflammation and epithelial dysfunction have been observed in individuals and laboratory animals with iron deficiency. Chronic inflammation has been associated with greater risk of cancer in many organs of the body. It has also been noted that serum ferritin levels are elevated and serum iron concentrations are decreased with tumor progression in head-and-neck carcinomas and thus heme can be used as a follow-up tool for patients along with nutritional assessment.
Vitamin B12 is produced as hydroxocobalamin within bacteria, and its conversion to methylcobalamin and 5'-deoxyadenosylcobalamin, enzymatically active cofactor forms, occurs within the body. Cyanocobalamin, the fourth vitamer of Vitamin B12, can be metabolized in the body to an active coenzyme form and used in food supplements. The most well-known manifestation of cobalt deficiency in oral cavity is pernicious anemia which is characterized by glossitis, burning sensation, beefy red tongue present in the form of patches or completely red tongue which is also referred to as Hunters' or Moeller's glossitis and shallow ulcers.
In the present study, Vitamin B12 deficiency was seen in 52.5% of the study group. In a South African study, Seedat reported that serum Vitamin B12 and folate levels of OSMF patients were within normal limits. According to Rajendran et al., a subclinical Vitamin B complex deficiency has been suspected in cases of OSMF with vesiculation and ulcerations of the oral cavity. The deficiency could be precipitated by the effect of defective nutrition due to impaired food intake in advanced cases and may be the effect, rather than the cause of the disease. They also reported that Vitamin and iron deficiency together with malnourished state of the host leads to derangement in the inflammatory reparative response of the lamina propria with resultant defective healing and scarification, which ultimately lead to OSMF.
In the present study, most of the patients consumed gutkha which is a combination of areca nut and tobacco. One of the harmful effects of tobacco is depletion in the levels of micronutrients. Low Vitamin B12 levels may not be the sole initiating factor, but may act synergistically with carcinogens and genetic and environmental factors, increasing the rate of malignant transformation. It plays an important role in protection against cancer due to its role in DNA synthesis and repairing damaged DNA. The deficiencies may not be carcinogenic but increase the susceptibility to action by other carcinogens.,
The prevalence of OSMF in this part of Gujarat is considerably high owing to the increased consumption of areca nut and tobacco products across all age groups irrespective of gender. However, there are very few studies being carried out to investigate the role of the hematological indices. Therefore, this study attempted to evaluate the hematological profile in OSMF patients as it can aid in the treatment and improving the prognosis of this chronic debilitating disorder. A significant finding in the present study is the presence of IDA (92.5%) and Vitamin B12 deficiency (52.5%) in the study group as compared to the control group. The hematological parameters are deterrent factors in maintaining the integrity of oral mucosa and in the progression of OSMF. The limitation of the study is the small sample size, and future studies should be carried out on larger number of patients.
| Conclusion|| |
OSMF is associated with a high malignant transformation rate (7%–13%). Low serum iron levels have been linked with head-and-neck cancers, which may further aggravate the condition. Therefore, it is imperative to detect and treat the low serum iron and Vitamin B12 levels in OSMF patients. In addition to the conventional treatment modalities in OSMF, iron and vitamin supplementation must be followed as a routine treatment protocol. Future clinical trials should be targeted toward the systemic use of iron and vitamins in OSMF patients. Nutritional supplementation with iron and Vitamin B12 is a form of chemoprevention, halting the disease progression, thereby preventing malignant transformation.
We would like to acknowledge Dr. Rashmi Phulare, Professor and Head, Department of Oral Pathology and Microbiology, for helping us to carry out the hematological investigations.
Financial support and sponsorship
This study was funded by the institution,Manu Bhai Patel Dental College,Hospital and Oral Research Centre, Vadodara, Gujarat, India.
Conflicts of interest
There are no conflicts of interest.
| References|| |
Misra SP, Misra V, Dwivedi M, Gupta SC. Oesophageal subepithelial fibrosis: An extension of oral submucosal fibrosis. Postgrad Med J 1998;74:733-6.
Murti PR, Bhonsle RB, Gupta PC, Daftary DK, Pindborg JJ, Mehta FS. Aetiology of oral submucous fibrosis with special reference to the role of areca nut chewing. J Oral Pathol Med 1995;24:145-52.
Cox SC and Walker DM. Oral submucous fibrosis. A review. Australian Dent J 1996;41:294-9.
Kiran Kumar K, Saraswathi TR, Ranganathan K, Uma Devi M, Elizabeth J. Oral submucous fibrosis: A clinic-histopathological study in Chennai. IJDR 2007;8;108-11.
Rajendran R, Vijayakumar T, Vasudevan DM. An alternative pathogenetic pathway for oral submucous fibrosis (OSMF). Med Hypotheses 1989;30:35-7.
Wahi PN, Kapur VL, Luthra UK, Srivastava MC. Submucous fibrosis of the oral cavity. 2. Studies on epidemiology. Bull World Health Organ 1966;35:793-9.
Bhardwaj D, Dinkar AD, Satoskar SK, Desai SR. Serum Iron and haemoglobin estimation in oral submucous fibrosis and Iron deficiency anaemia: A diagnostic approach. J Clin Diagn Res 2016;10:ZC54-8.
Huang S, Ling T, Wu H. Experimental study on aqueous areca nut extracts inducing OSMF in rats. Effect of mast cells on collagen metabolism. Hua Xi Kou Qiang Yi Xue Za Zhi 1997;15:94-6.
Ramanathan K. Oral submucous fibrosis e an alternative hypothesis as to its causes. Med J Malaysia 1981;36:243-5.
Ganapathy KS, Gurudath S, Balikai B, Ballal S, Sujatha D. Role of iron deficiency in oral submucous fibrosis: An initiating or accelerating factor. JIAOMR 2011;23:25-8.
Arakeri Thomas D, Aljababa AS, Hunasgi S, Rai KK, Rai KK, Hale B et al
. TFM classification and staging of oral submucous fibrosis: A new proposal. J Oral Path Med 2018;47:403-9.
Tsiminis G, Schartner E, Brooks JL, Hutchinson MR. Measuring and tracking vitamin B12: A review of current methods with a focus on optical spectroscopy. Applied Spectroscopy Rev 2017;52:439-55.
More CB, Rao NR. Proposed clinical definition for oral submucous fibrosis. J Oral Biol Craniof Res 2019;9:311-14.
Ranganathan K, Devi MU, Joshua E, Kirankumar K, Saraswati TR. Oral submucous fibrosis: A case control study in Chennai, South India. J Oral Pathol Med 2004;33:274-7.
Babu S, Bhat RV, Kumar PU, et al
. A comparative clinicopathological study of oral submucous fibrosis in habitual chewers of pan masala and betel quid. Clin Toxicol 1996;34:317e-22.
Shah N, Sharma PP. Role of chewing and smoking habits in the etiology of oral submucous fibrosis (OSMF): A case control study. J Oral Pathol Med 1998;27:475e-9.
Javed F, Chotai M, Mehmood A, Almas K. Oral mucosal disorders associated with habitual gutka usage: A review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010;109:857-64.
Wang YP, Wu YC, Cheng SJ, Chen HM, Sun A, Chang JY. High frequencies of vitamin B12 and folic acid deficiencies and gastric parietal cell antibody positivity in oral submucous fibrosis patients. J Formos Med Assoc 2015;114:813-9.
Tadakamadla J, Kumar S, GP M. Evaluation of serum copper and iron levels among oral submucous fibrosis patients. Med Oral Patol Oral Cir Bucal 2011;16:e870-3.
Anuradha CD, Devi CS. Serum protein, ascorbic acid Iron tissue collagen in oral submucous fibrosis-a preliminary study. Indian J Med Res 1993;98:147-51.
Rajendran R, Vasudevan DM, Vijayakumar T. Serum levels of iron and proteins in oral submucous fibrosis (OSMF). Ann Dent 1990;49:23-5, 45.
Thakur M, Guttikonda VR. Estimation of hemoglobin, serum iron, total iron-binding capacity and serum ferritin levels in oral submucous fibrosis: A clinicopathological study. J Oral Maxillofac Pathol 2017;21:30-5.
] [Full text]
Karthik H, Nair P, Gharote HP, Agarwal K, Ramamurthy Bhat G, Kalyanpur Rajaram D. Role of hemoglobin and serum iron in oral submucous fibrosis: A clinical study. ScientificWorldJournal 2012;2012:254013.
Khanna SS, Karjodkar FR. Circulating Immune Complexes and trace elements (Copper, Iron and Selenium) as markers in Oral precancer and cancer: A randomized, controlled clinical trial. J Indian Acad Oral Med Radiol 2005;17:161-4. [Full text]
Lavina T, Anjana B, Vaishali K. Hemoglobin levels in patients with oral submucous fibrosis. J Indian Acad Oral Med Radiol 2007;19:329-33.
Rupak S, Giju GB, Sheba P, Kiran KK. Oral submucous fibrosis and iron deficiency anaemia relationship revisited-results from an Indian study. E J Dent 2012;2:159-65.
Vasudevan DM and Sreekumari S, Text Book of Biochemistry for Medical Students. 5th ed, New Delhi, India: Jaypee Brothers Medical Publishers; 2007
Desai VD, Kumar S, Bathi RJ, Gaurav I, Sharma R. Molecular analysis of trace elements in oral submucous fibrosis and future perspectives. Univ Res J Dent 2014;4:26-35. [Full text]
Neville BD, Damm DD, Allen CM, and Bouquot JE, Oral and Maxillofacial Pathology. 3rd
ed. Chennai, India: Elsevier; 2009.
Kakar PK, Puri RK, Venkatachalam VP. Oral submucous fibrosis-treatment with hyalase. J Laryngol Otol 1985;99:57-9.
Trivedy C, Warnakulasuriya KA, Hazarey VK, Tavassoli M, Sommer P, Johnson NW. The upregulation of lysyl oxidase in oral submucous fibrosis and squamous cell carcinoma. J Oral Pathol Med 1999;28:246-51.
Bhattacharya PT, Khaitan T, Sarkar SB, Sinha R. Oral submucous fibrosis secondary to Iron deficiency anemia: A case report, etiopathogenesis and management. J Nutr Health Aging 2016;20:205-8.
Prá D, Rech Franke SI, Pegas Henriques JA, Fenech M. A possible link between iron deficiency and gastrointestinal carcinogenesis. Nutr Cancer 2009;61:415-26.
Dedon PC, Tannenbaum SR. Reactive nitrogen species in the chemical biology of inflammation. Arch Biochem Biophys 2004;423:12-22.
Thomas G, Hashibe M, Jacob BJ, Ramadas K, Mathew B, Sankaranarayanan R, et al
. Risk factors for multiple oral premalignant lesions. Int J Cancer 2003;107:285-91.
Lombaert Nelson D, Van Hummelen P, Kirsch-Volders M. In vitro
expression of hard metal dust (WC-Co)-responsive genes in human peripheral blood mononucleated. Cells Toxicol Applied Pharmacol 2008;227:299-312.
Shafer WG, Hine MK, Levy BM. A Textbook of Oral Pathology. 4th
ed. Chennai, India: Elsevier India; 2004.
Seedat HA. Oral Submucous Fibrosis in Durban, Natal: A Study of its Epidemiology, Etiology and Morphological Features. Thesis. Stellenbosch, South Africa: University of Stellenbosch; 1985.
Hetch SS. Tobacco smoke carcinogens and lung cancer Natl Cancer Inst 1999;91:1194-210.
Eto I, Krumdieck CL. Role of vitamin B12 and folate deficiencies in carcinogenesis. Adv Exp Med Biol 1986;206:313-30.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]