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1.
Rev. ADM ; 79(1): 54-58, ene.-feb. 2022. ilus
Article in Spanish | LILACS | ID: biblio-1362610

ABSTRACT

Introducción: La hiperplasia gingival es una condición benigna caracterizada por el aumento de volumen de la encía. Algunos fármacos, factores genéticos, aparatología y placa dentobacteriana son factores que pueden inducir esta condición. Objetivo: Devolver la anatomía a la encía brindando una mejor estética y permitiendo una óptima higiene oral. Material y métodos: Paciente masculino de 20 años de edad con antecedentes de fenitoína presenta aumento de volumen en la encía. Resultados: Se obtuvieron resultados estéticos y funcionales satisfactorios con el tratamiento quirúrgico y el uso de membrana de celulosa oxidada. Conclusión: En el manejo de la hiperplasia gingival es importante el enfoque no quirúrgico como control de placa dentobacteriana y medidas de higiene del mismo paciente (AU)


Introduction: Gingival hyperplasia is a benign condition characterized for the grown on the gingival volume. Some drugs, genetic, orthodontic and dental plaque are some factors that can induce this condition. Objective: To return the gingival anatomy, providing a better aesthetic allowing also good oral hygiene. Material and methods: A male 20 years of age with medical history of phenytoin display grown on the gingival volume. Results: Aesthetic and functional results were achieved with the surgical treatment and the oxidized cellulose membrane. Conclusion: In the gingival hyperplasia management is important de non-surgical approach, as dental plaque control and oral hygiene of the patient (AU)


Subject(s)
Humans , Female , Adult , Phenytoin/adverse effects , Cellulose, Oxidized , Gingival Hypertrophy/chemically induced , Gingivectomy , Esthetics, Dental , Membranes, Artificial , Mexico
2.
Clin Adv Periodontics ; 12(2): 130-133, 2022 06.
Article in English | MEDLINE | ID: mdl-32852892

ABSTRACT

INTRODUCTION: Gingival enlargement (GE) due to anti-epileptic drugs (AEDs) shows a high prevalence rate. However, lamotrigine, a newer AED, has not shown to induce GE. The present case report describes a rare case of GE in a patient with epilepsy under lamotrigine therapy for the past 3 years. CASE PRESENTATION: In this report, successful management of lamotrigine-influenced GE in a 24-year-old patient with epilepsy by gingivectomy followed by stringent oral hygiene protocol is presented. CONCLUSION: The present case report suggests that, even this newer AED can cause GE and the oral hygiene status of the patients could be an important triggering factor.


Subject(s)
Epilepsy , Gingival Hyperplasia , Gingival Hypertrophy , Gingival Overgrowth , Anticonvulsants/adverse effects , Epilepsy/chemically induced , Epilepsy/drug therapy , Epilepsy/epidemiology , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/drug therapy , Gingival Hypertrophy/chemically induced , Gingival Hypertrophy/drug therapy , Gingival Overgrowth/chemically induced , Gingival Overgrowth/drug therapy , Humans , Lamotrigine/adverse effects , Young Adult
3.
Ann Hematol ; 100(4): 933-939, 2021 Apr.
Article in English | MEDLINE | ID: mdl-33420879

ABSTRACT

First-line treatment of aplastic anemia(AA) and for AA patients ineligible for hematopoietic stem cell transplantation (HSCT) has consisted of antithymocyte globulin (ATG), the calcineurin inhibitor cyclosporine A (CsA), and more recently eltrombopag. However, at our institution, we have successfully substituted another calcineurin inhibitor, tacrolimus, as a part of immunosuppressive threatment (IST) for AA due to more favorable toxicity profile. Since there is limited data on the use of tacrolimus in aplastic anemia, we conducted a retrospective review of twenty patients treated with tacrolimus-based immunosuppressive therapy (IST) as a first- or second-line treatment. The overall response rate was comparable to that of patients treated with CsA (18 patients). However, there were no cutaneous side effects observed in patients receiving tacrolimus, a relatively common finding with CsA use. Our data suggest that tacrolimus-based IST is a potential option in AA and might have a more favorable toxicity profile compared to CsA.


Subject(s)
Anemia, Aplastic/drug therapy , Benzoates/therapeutic use , Hydrazines/therapeutic use , Immunosuppressive Agents/therapeutic use , Pyrazoles/therapeutic use , Tacrolimus/therapeutic use , Adult , Aged , Antilymphocyte Serum/adverse effects , Antilymphocyte Serum/therapeutic use , Benzoates/adverse effects , Cyclosporine/adverse effects , Cyclosporine/therapeutic use , Drug Eruptions/etiology , Female , Gingival Hypertrophy/chemically induced , Hirsutism/chemically induced , Humans , Hydrazines/adverse effects , Immunosuppressive Agents/adverse effects , Male , Middle Aged , Pyrazoles/adverse effects , Retrospective Studies , Tacrolimus/adverse effects
5.
Indian Heart J ; 67(5): 491-2, 2015.
Article in English | MEDLINE | ID: mdl-26432745

ABSTRACT

Gingival hypertrophy (GH) is a well-known physical manifestation due to inflammatory conditions, pregnancy, vitamin C deficiency, systemic diseases like leukemia, Wegners granulomatosis, and various drugs like anticonvulsants, immunosuppresant, and calcium channel blockers (CCBs).We present here a case of a 45-year-old woman, who has been taking Amlodipine 10mg once a day together with Atenelol 50mg per day for one and half years, and has subsequently developed gum hypertrophy. This manifestation was reversed after stopping of Amlodipine. Though this case presentation is described in literature, we hereby present it in a pictorial form, to sensitize the treating physician toward it.


Subject(s)
Amlodipine/adverse effects , Diagnostic Errors , Gingiva/pathology , Gingival Hypertrophy/chemically induced , Amlodipine/therapeutic use , Calcium Channel Blockers/adverse effects , Calcium Channel Blockers/therapeutic use , Female , Gingiva/drug effects , Gingival Hypertrophy/diagnosis , Humans , Hypertension/drug therapy , Middle Aged
6.
BMJ Case Rep ; 20152015 Oct 16.
Article in English | MEDLINE | ID: mdl-26475882

ABSTRACT

Gum hypertrophy is a well-known and important adverse effect of phenytoin therapy in a neurosurgical patient. We present an interesting case of a 21-year-old man who, following head injury after a road traffic accident, developed status epilepticus diagnosed with gum hypertrophy in the jaws, with ongoing antiepileptics. He was managed conservatively as per hospital protocol.


Subject(s)
Anticonvulsants/adverse effects , Gingival Hypertrophy/chemically induced , Phenytoin/adverse effects , Status Epilepticus/drug therapy , Accidents, Traffic , Anticonvulsants/therapeutic use , Craniocerebral Trauma/complications , Gingival Hypertrophy/therapy , Humans , Male , Phenytoin/therapeutic use , Status Epilepticus/etiology , Young Adult
7.
Minerva Stomatol ; 63(3): 59-67, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24632797

ABSTRACT

AIM: In the present immunohistochemical study, the expression of vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67 in the gingival tissues of renal transplant patients treated with cyclosporin A was assessed. Gingival overgrowth (GO) frequently occurs in transplant patients receiving immunosuppressive drugs such as cyclosporine and this gingival inflammation might play an important role in the pathogenesis of drug-induced GO. METHODS: Twenty-eight human gingival biopsies were taken from healthy patients with chronic periodontitis (N.=14 control group), and from renal transplant recipients treated with cyclosporin A (N.=14 test group). The retrieved specimens were immunohistochemically processed and stained for vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67. RESULTS: The levels of vascular endothelial growth factor, nitric oxide synthase 1 and 3, and Ki-67 were found to be significantly different among groups (P>0.001), with patients treated with cyclosporin A showing higher levels of all the analyzed markers compared to control group. CONCLUSION: In summary, the data from this pilot study suggests that the investigated factors have a role in the inflammation processes associated to immunosuppressive therapy. However, further studies with a larger sample population need to be conducted for an exhaustive knowledge of the mechanisms leading to GO.


Subject(s)
Cyclosporine/adverse effects , Gingival Hypertrophy/chemically induced , Immunosuppressive Agents/adverse effects , Ki-67 Antigen/analysis , Kidney Transplantation , Nitric Oxide Synthase Type III/analysis , Nitric Oxide Synthase Type II/analysis , Postoperative Complications/chemically induced , Vascular Endothelial Growth Factor A/analysis , Adult , Aged , Biomarkers , Biopsy , Cyclosporine/pharmacology , Female , Gingiva/blood supply , Gingiva/pathology , Gingival Hypertrophy/metabolism , Gingival Hypertrophy/pathology , Humans , Immunoenzyme Techniques , Immunosuppressive Agents/pharmacology , Inflammation , Male , Middle Aged , Neovascularization, Physiologic , Periodontitis/metabolism , Postoperative Complications/metabolism , Postoperative Complications/pathology , Young Adult
8.
Fogorv Sz ; 106(2): 61-70, 2013 Jun.
Article in Hungarian | MEDLINE | ID: mdl-24344562

ABSTRACT

INTRODUCTION: Gingival enlargement is a common form of periodontal tissue reaction to several irritating factors. The most common form is the drug related gingival hyperplasia--nevertheless the heredity gingival fibromatosis and hematological cases can also occur and might impose a challenge to periodontists. After a short literature summary three Case reports are presented. The first case is a drug related gingival overgrowth in a young kidney transplant women who took Cyclosporin-A. The excessive mass of fibrotic tissue was removed by a series of internal beveled incision and the oral and buccal gingival flaps were united with sutures. The healing was uneventful and during the follow up patient's compliance and oral hygiene was superb. The second case is a very severe antihypertensive drug related gingival overgrowth in a 62 years old man interfering with the closure of his lip and corrected with a combination of conventional gingivectomy and internal reverse beveled incision both and Ca-channel blockers. The third case is a 42 years old woman with chronic idiopathic hemolytic anemia who presented a sudden onset acute excessive generalized gingival enlargement accompanied with severe pain and fever. At admission she was suspect for leukemia. After obtaining biopsy samples and having negative histology the soft tissue mass was removed under general anesthesia with conventional gingivectomy technique, but after a couple of days the severe pain and gingival swelling recurred. With administering systemic corticosteroid therapy (32 mg Medrol), the gingiva healed in five days and the one year follow-up showed a stable hematological and periodontal status. Today the more conservative internal beveled incision is preferred over the conventional gingivectomy in the most cases because it provides a more predictable healing and better esthetics. The recurrence of the drug related gingival hyperplasia can be anticipated by meticulous postoperative individual oral hygiene and regular supportive therapy. CONCLUSION: The combined conservative and surgical therapy leads to predictable postoperative result even in very severe systematically motivated gingival enlargements, nevertheless the successful patients management needs good cooperation with medical doctors and with the patients themselves.


Subject(s)
Gingival Hyperplasia/etiology , Gingival Hyperplasia/surgery , Gingival Hypertrophy/etiology , Gingival Hypertrophy/surgery , Gingivectomy , Adult , Aged , Anemia, Hemolytic/complications , Antihypertensive Agents/administration & dosage , Antihypertensive Agents/adverse effects , Calcium Channel Blockers/administration & dosage , Calcium Channel Blockers/adverse effects , Cyclosporine/administration & dosage , Cyclosporine/adverse effects , Female , Fever/etiology , Gingival Hyperplasia/chemically induced , Gingival Hyperplasia/complications , Gingival Hypertrophy/chemically induced , Gingival Hypertrophy/complications , Gingivectomy/methods , Granuloma/complications , Humans , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/adverse effects , Kidney Transplantation , Male , Middle Aged , Oral Hygiene , Pain/etiology , Suppuration , Treatment Outcome
9.
Minerva Stomatol ; 62(11-12): 419-30, 2013.
Article in English, Italian | MEDLINE | ID: mdl-24212412

ABSTRACT

AIM: The aim of the present study was to highlight the relationship between the level of oral hygiene and the context in which the patient receives dental treatment, demonstrating that home service is essential and effective to decrease the incidence of periodontal diseases. METHODS: The study was initially conducted on a heterogeneous sample of patients including 48 individuals with psycho-motor deficits. The study included 28 males (58.3%) and 20 females (41.7%) aged between 18 and 50 years, coming from two different sites ("Fa.Di.Vi… e oltre" and "Dentistry Unit, Istituto G. Gaslini" in Genoa). The patients were evaluated during the period 2008-2009. After this first pilot study, a clinical trial was conducted within the educational center "Il Granello", with the participation of 20 patients with disabilities. RESULTS: This study demonstrates that home assistance is essential and effective to decrease the incidence of those periodontal diseases induced by bacterial dental plaque accumulation, and associated with aggravating factors like the repeated use of drugs, such as benzodiazepines, phenylhydantoin, and cyclosporin A, that cause gingival hypertrophia. CONCLUSION: This study was proposed to demonstrate that the availability of a dental service within institutions could improve not only the dental-periodontal conditions of the participants, but also decrease the admission of these subjects to hospitals, contributing to the reduction of public expenditure by the Health Care System.


Subject(s)
Disabled Persons , Home Care Services , Oral Hygiene/methods , Patient Education as Topic , Periodontal Diseases/prevention & control , Self Care , Adolescent , Adult , Day Care, Medical , Dental Plaque Index , Female , Gingival Hemorrhage/epidemiology , Gingival Hemorrhage/prevention & control , Gingival Hypertrophy/chemically induced , Gingival Hypertrophy/epidemiology , Humans , Male , Middle Aged , Mouth/microbiology , Oral Hygiene/education , Periodontal Diseases/epidemiology , Periodontal Index , Pilot Projects , Young Adult
10.
Quintessence Int ; 43(10): 879-85, 2012.
Article in English | MEDLINE | ID: mdl-23115767

ABSTRACT

OBJECTIVE: To compare the current (t1) periodontal status of post-liver transplantation patients to their status 10 years earlier (t0). METHOD AND MATERIALS: Seventeen patients 45 to 71 years of age who were evaluated approximately 10 years previously were enrolled in the study. All subjects had undergone a liver transplantation 1 to 10 years prior to the initial examination (t0). Clinical and radiographic parameters were recorded for the Ramfjord Index teeth and compared between t0 and t1, including Plaque Index (PI), Gingival Index (GI), probing depth (PD), clinical attachment level (CAL), and gingival overgrowth (GO). Bone loss was measured on digitized images of panoramic radiographs. RESULTS: Mean PI, GI, CAL, and GO were slightly lower at t1 than at t0; however, these differences were not statistically significant (P > .05, Student t test for paired observations). The mean PD was reduced at t1 (2.43 ± 0.18 mm) compared with t0 (3.35 ± 0.22 mm), which was statistically significant (P = .001, Student t test for paired observations). To the contrary, the mean radiographic bone loss at t1 was higher than at t0 (5.61 vs 4.48 mm, respectively), which was also statistically significant (P = .017). Tooth loss was observed in some of these patients, ranging from 0 to 4 during the 10 years of follow-up, which amounted to an annual rate of 0.24 teeth per patient. CONCLUSION: Post-liver transplantation patients maintained stable clinical periodontal parameters during a 10-year period; however, some radiographic bone loss occurred during this time.


Subject(s)
Alveolar Bone Loss , Gingival Hypertrophy/chemically induced , Immunosuppressive Agents/adverse effects , Liver Transplantation , Aged , Dental Plaque , Female , Follow-Up Studies , Humans , Liver Transplantation/adverse effects , Longitudinal Studies , Male , Middle Aged , Periodontal Attachment Loss , Periodontal Index , Periodontal Pocket , Tooth Loss
11.
Rev. Fundac. Juan Jose Carraro ; 17(36): 14-19, sept.-oct. 2012. ilus
Article in Spanish | LILACS | ID: lil-684946

ABSTRACT

El término agrandamiento gingival por fármacos se refiere a un crecimiento anormal de la encía, secundario al uso de una medicación sistémica. Si bien se reporta una larga lista de medicamentos relacionados, se encontró una fuerte asociación sólo con la Fenitoína , la Nifedipina y la Ciclosporina A. La prevalencia del Agrandamiento Gingival varía ampliamente, sin embargo la prevalencia relacionada con el uso de la Fenitoína es aproximadamente del 50 por ciento. La Nifedipina y la ciclosporina producen cambios en el 25 por ciento de los pacientes tratados. Existe controversia entre la dosis y el riesgo o severidad del Agrandamiento.El grado de Agrandamiento gingival parece estar relacionado con la susceptibilidad del paciente y el grado dehigiene bucal de éste. Después de 1 a 3 meses de iniciada la medicación del fármaco los agrandamientos originadosen la papila interdental, se expande afectando otras áreas de la encía llegando a cubrir en casos extremosuna porción importante de los dientes principalmente en los segmentos anteriores por vestibular. El uso discontinuo de la medicación por el médico de cabecera y más aún la sustitución del fármaco por otroresulta en la regresión y el cese del Agrandamiento.


Subject(s)
Humans , Male , Female , Cyclosporine/adverse effects , Phenytoin/adverse effects , Nifedipine/adverse effects , Gingival Overgrowth/chemically induced , Folic Acid/therapeutic use , Gingival Hyperplasia/chemically induced , Gingival Hypertrophy/chemically induced , Gingival Overgrowth/epidemiology
12.
Rev. Fundac. Juan Jose Carraro ; 17(36): 14-19, sept.-oct. 2012. ilus
Article in Spanish | BINACIS | ID: bin-128659

ABSTRACT

El término agrandamiento gingival por fármacos se refiere a un crecimiento anormal de la encía, secundario al uso de una medicación sistémica. Si bien se reporta una larga lista de medicamentos relacionados, se encontró una fuerte asociación sólo con la Fenitoína , la Nifedipina y la Ciclosporina A. La prevalencia del Agrandamiento Gingival varía ampliamente, sin embargo la prevalencia relacionada con el uso de la Fenitoína es aproximadamente del 50 por ciento. La Nifedipina y la ciclosporina producen cambios en el 25 por ciento de los pacientes tratados. Existe controversia entre la dosis y el riesgo o severidad del Agrandamiento.El grado de Agrandamiento gingival parece estar relacionado con la susceptibilidad del paciente y el grado dehigiene bucal de éste. Después de 1 a 3 meses de iniciada la medicación del fármaco los agrandamientos originadosen la papila interdental, se expande afectando otras áreas de la encía llegando a cubrir en casos extremosuna porción importante de los dientes principalmente en los segmentos anteriores por vestibular. El uso discontinuo de la medicación por el médico de cabecera y más aún la sustitución del fármaco por otroresulta en la regresión y el cese del Agrandamiento. (AU)


Subject(s)
Humans , Male , Female , Gingival Overgrowth/chemically induced , Phenytoin/adverse effects , Cyclosporine/adverse effects , Nifedipine/adverse effects , Gingival Hyperplasia/chemically induced , Gingival Hypertrophy/chemically induced , Gingival Overgrowth/epidemiology , Folic Acid/therapeutic use
13.
J Periodontal Res ; 47(6): 776-82, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22897219

ABSTRACT

BACKGROUND AND OBJECTIVE: The objective of this study was to analyze the concordance of the vertical gingival overgrowth index (GOi) and the horizontal Miranda & Brunet index (MBi) and to compare their reliability and reproducibility for an early diagnosis of gingival enlargement. A wide range of methods has been employed to determine the severity of drug-induced gingival enlargement (DIGE) that has resulted in uncertainty with regard to the prevalence of this side effect. In recent studies, different indices have been used to grade DIGE. The large variability observed between studies and the differences between vertical and horizontal gingival-enlargement measurements could be the result of the use of nonreliable indices during the measurement process. Some indices involve invasive procedures that require many measurements, or even a data-processing system, while others are less convenient and technically expensive and complex. In previous studies we used two complementary indices - the vertical GOi and the horizontal MBi. The results of these studies found some differences between both indices, with the MBi rendering higher estimates of DIGE prevalence that was attributed to its greater sensitivity for the detection of minimal changes in gingival thickness. To our knowledge, there are no studies comparing different measurement indices for gingival enlargement that are supported by statistical concordance analysis. MATERIAL AND METHODS: Twelve plaster casts from patients who had worn orthodontic brackets, and who had different degrees of chronic inflammatory gingival enlargement, were analyzed. Three previously trained examiners registered twice the degree of buccal overgrowth, using the GOi and MBi, in all cast models with a minimum interval of 7 d between the first and the second evaluation. In total, from each cast, measurements from 16 gingival sites were taken using the GOi, and from nine gingival units (mesial and distal sites measurements) using the MBi. Concordance analysis of the registered measurements (intra-examiner and among examiners) for each index and between indices was assessed using the nonweighted Kappa index with a confidence interval of 95%. RESULTS: We obtained 648 values for the GOi and the MBi. The overall score 0 (indicating absence of enlargement) was 32.7% and 19.8% for GOi and MBi, respectively, score 1 (light/moderate) was 39.7% and 48.1%, and score 2 (severe) was 27.6% and 32.1%. Concordance analysis for each index showed intra-examiner Kappa values of 0.820 for the GOi and 0.830 for the MBi. Interexaminer Kappa values were 0.720 for the GOi and 0.770 for the MBi. Concordance between indices showed Kappa values for the same examiner of 0.600, whereas concordance among different examiners was 0.550. Discrepancies between indices indicated a systematic skew, with 79-82.1% of discrepancy associated with a higher value for the MBi compared with the GOi. CONCLUSION: Both gingival enlargement indices analyzed are reliable, complementary and applicable for measuring gingival overgrowth. However, the MBi shows, with fewer measurements, a greater sensitivity than the GOi for the detection of the early stages of gingival enlargement, being adequate for the screening of large populations at risk.


Subject(s)
Gingival Hypertrophy/diagnosis , Periodontal Index , Analysis of Variance , Cephalometry/methods , Confidence Intervals , Dimensional Measurement Accuracy , Gingival Hypertrophy/chemically induced , Humans , Observer Variation , Reference Values , Reproducibility of Results , Sensitivity and Specificity , Severity of Illness Index
16.
Oral Dis ; 16(4): 396-401, 2010 May.
Article in English | MEDLINE | ID: mdl-20233320

ABSTRACT

OBJECTIVES: Cyclosporine A (CsA) is used as an immunosuppressive agent and its prominent side effect is the induction of gingival overgrowth. Type I plasminogen activator inhibitor (PAI-1) has shown to play an important role in CsA-induced gingival overgrowth. However, little is known about whether factors can modulate CsA-induced PAI-1 expression. METHODS: Cytotoxicity, reverse transcriptase-polymerase chain reaction, and enzyme-linked immunosorbent assay were used to investigate the effects of Human gingival fibroblasts (HGFs) exposed to CsA. In addition, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, interlukin-1alpha, tumor necrosis factor-alpha, mitogen-activated protein kinase kinase (MEK) inhibitor U0126, signal-regulated protein kinase (ERK) inhibitor PD98059 and cell-permeable glutathione precursor N-acetyl-L-cysteine (NAC) were added to test how they modulated the effects of CsA-induced PAI-1 expression. RESULTS: The concentration of CsA higher than 500 ng ml(-1) demonstrated cytotoxicity to HGFs (P < 0.05). Periodontal pathogens as well as proinflammatory cytokines were found to increase the CsA-induced PAI-1 mRNA and protein expression (P < 0.05). Pharmacological agents NAC, U0126, and PD98059 were found to decrease the CsA-induced PAI-1 mRNA and protein expression (P < 0.05). CONCLUSIONS: Cyclosporine A (CsA) may predispose to gingival overgrowth under inflammatory environments. The regulation of PAI-1 expression induced by CsA might be critically related with the intracellular glutathione and the ERK-MAPK pathway.


Subject(s)
Cyclosporine/pharmacology , Fibroblasts/drug effects , Gingiva/drug effects , Gingival Hypertrophy/prevention & control , Immunosuppressive Agents/pharmacology , Plasminogen Activator Inhibitor 1/metabolism , Cells, Cultured , Cyclosporine/adverse effects , Dose-Response Relationship, Drug , Epithelial Cells/cytology , Epithelial Cells/drug effects , Epithelial Cells/metabolism , Fibroblasts/cytology , Fibroblasts/metabolism , Gingiva/cytology , Gingiva/metabolism , Gingival Hypertrophy/chemically induced , Gingival Hypertrophy/metabolism , Humans , Immunosuppressive Agents/adverse effects , Plasminogen Activator Inhibitor 1/genetics , RNA, Messenger/analysis
17.
Nefrologia ; 29(5): 474-8, 2009.
Article in Spanish | MEDLINE | ID: mdl-19820760

ABSTRACT

AIM: To assess gingival overgrowth prevalence and severity in a group of kidney transplant (KT) patients, and analyze the effect of immunosuppressor drugs Cyclosporin A (CsA), Tacrolimus (Tac), Sirolimus (Siro), Azathioprine (Aza) and Mofetil Mycophenolate on this complication. METHODS: Gingival overgrowth presence and severity was classified, and the impact of immunosuppressor drugs, age, oral hygiene, verapamil and nifedipine on this condition was analyzed by multiple logistic regression. RESULTS: 172 KT pts. were examined; 137 used CsA, 25 Tac, 6 Sirolimus, 107 Aza and 56 MMF. Gingival overgrowth prevalence was 59.1% on CsA, 12.0% on Tac, and 16.7% on Sirolimus. CsA odds ratio (OR) 15.2, age <45 OR 5.6, and poor oral hygiene OR 3.2, increased, and Aza OR 0.05 and MMF OR 0.03, decreased GO prevalence. CONCLUSIONS: Aza and MMF effect was a significant protection against GO prevalence in this group of KT patients.


Subject(s)
Azathioprine/adverse effects , Cyclosporine/adverse effects , Gingival Hypertrophy/chemically induced , Immunosuppressive Agents/adverse effects , Kidney Transplantation , Mycophenolic Acid/analogs & derivatives , Adult , Cross-Sectional Studies , Female , Gingival Hypertrophy/epidemiology , Humans , Male , Mycophenolic Acid/adverse effects , Severity of Illness Index
18.
Spec Care Dentist ; 29(2): 80-4, 2009.
Article in English | MEDLINE | ID: mdl-19284507

ABSTRACT

An immunoperoxidase technique was used to compare the number of CD1a+ and factor XIIIa+ dendritic cells (DCs), and CD68+ Macrophages (M) in 30 gingival samples from subjects with clinically healthy periodontitium (HP) and 10 samples from subjects with drug-induced gingival enlargement (DIGE). Fewer CD1a+ and factor XIIIa+ DCs were found in areas with inflammatory infiltration (II) of the lamina propria (LP) in the group with immunosuppressed DIGE (IDIGE) compared to the group with HP. In the sulcular and junctional/pocket epithelia, the number of CD1a+ DCs was decreased in the group with IDIGE (p<0.05). There was a tendency toward a reduced number of CD1a+ DCs and CD68+ M in areas without inflammatory infiltrate of the LP in the group with IDIGE. The alterations in the number of antigen-presenting cells (APCs) may be the reason for the decreased periodontal inflammation and breakdown clinically observed in subjects who are immunosuppressed.


Subject(s)
Antigen-Presenting Cells/pathology , Gingival Hypertrophy/chemically induced , Immunosuppressive Agents/adverse effects , Adult , Antigen-Presenting Cells/immunology , Antigens, CD/analysis , Antigens, CD1/analysis , Antigens, Differentiation, Myelomonocytic/analysis , Dendritic Cells/immunology , Dendritic Cells/pathology , Epithelial Attachment/immunology , Epithelial Attachment/pathology , Epithelium/immunology , Epithelium/pathology , Factor XIIIa/analysis , Female , Gingival Crevicular Fluid/immunology , Gingival Hypertrophy/immunology , Humans , Immunoenzyme Techniques , Langerhans Cells/immunology , Langerhans Cells/pathology , Macrophages/immunology , Macrophages/pathology , Male , Middle Aged , Periodontal Pocket/immunology , Periodontal Pocket/pathology , Periodontium/immunology , Periodontium/pathology
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