Effects of long-term use of HAART on oral health status of HIV-infected subjects
J Oral Pathol Med (2010) 39: 397–406 Background: The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy (HAART) on oral health status of HIV‐infected subjects. Methods: Oral examination and measurement of saliva flow rate of both unstimulated an...
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Published in | Journal of oral pathology & medicine Vol. 39; no. 5; pp. 397 - 406 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.05.2010
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Subjects | |
Online Access | Get full text |
ISSN | 0904-2512 1600-0714 1600-0714 |
DOI | 10.1111/j.1600-0714.2009.00875.x |
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Abstract | J Oral Pathol Med (2010) 39: 397–406
Background: The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy (HAART) on oral health status of HIV‐infected subjects.
Methods: Oral examination and measurement of saliva flow rate of both unstimulated and wax‐stimulated whole saliva were performed in HIV‐infected subjects with and without HAART, and in non‐HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long‐term use of HAART on oral health status of HIV‐infected subjects.
Results: One hundred and fifty‐seven HIV‐infected subjects – 99 on HAART (age range 23–57 years, mean 39 years) and 58 not on HAART (age range 20–59 years, mean 34 years) – and 50 non‐HIV controls (age range 19–59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV‐infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short‐term HAART (P < 0.01). The subjects with long‐term HAART were found to have a greater risk of having oral lesions than those with short‐term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05).
Conclusion: We conclude that long‐term HAART has adverse effects on oral health status of HIV‐infected subjects. |
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AbstractList | J Oral Pathol Med
(2010)
39
: 397–406
Background:
The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy (HAART) on oral health status of HIV‐infected subjects.
Methods:
Oral examination and measurement of saliva flow rate of both unstimulated and wax‐stimulated whole saliva were performed in HIV‐infected subjects with and without HAART, and in non‐HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long‐term use of HAART on oral health status of HIV‐infected subjects.
Results:
One hundred and fifty‐seven HIV‐infected subjects – 99 on HAART (age range 23–57 years, mean 39 years) and 58 not on HAART (age range 20–59 years, mean 34 years) – and 50 non‐HIV controls (age range 19–59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV‐infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short‐term HAART (
P
< 0.01). The subjects with long‐term HAART were found to have a greater risk of having oral lesions than those with short‐term HAART (
P
< 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (
P
< 0.05).
Conclusion:
We conclude that long‐term HAART has adverse effects on oral health status of HIV‐infected subjects. The aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy (HAART) on oral health status of HIV-infected subjects.BACKGROUNDThe aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy (HAART) on oral health status of HIV-infected subjects.Oral examination and measurement of saliva flow rate of both unstimulated and wax-stimulated whole saliva were performed in HIV-infected subjects with and without HAART, and in non-HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long-term use of HAART on oral health status of HIV-infected subjects.METHODSOral examination and measurement of saliva flow rate of both unstimulated and wax-stimulated whole saliva were performed in HIV-infected subjects with and without HAART, and in non-HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long-term use of HAART on oral health status of HIV-infected subjects.One hundred and fifty-seven HIV-infected subjects - 99 on HAART (age range 23-57 years, mean 39 years) and 58 not on HAART (age range 20-59 years, mean 34 years) - and 50 non-HIV controls (age range 19-59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV-infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short-term HAART (P < 0.01). The subjects with long-term HAART were found to have a greater risk of having oral lesions than those with short-term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05).RESULTSOne hundred and fifty-seven HIV-infected subjects - 99 on HAART (age range 23-57 years, mean 39 years) and 58 not on HAART (age range 20-59 years, mean 34 years) - and 50 non-HIV controls (age range 19-59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV-infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short-term HAART (P < 0.01). The subjects with long-term HAART were found to have a greater risk of having oral lesions than those with short-term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05).We conclude that long-term HAART has adverse effects on oral health status of HIV-infected subjects.CONCLUSIONWe conclude that long-term HAART has adverse effects on oral health status of HIV-infected subjects. J Oral Pathol Med (2010) 39: 397–406 Background: The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy (HAART) on oral health status of HIV‐infected subjects. Methods: Oral examination and measurement of saliva flow rate of both unstimulated and wax‐stimulated whole saliva were performed in HIV‐infected subjects with and without HAART, and in non‐HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long‐term use of HAART on oral health status of HIV‐infected subjects. Results: One hundred and fifty‐seven HIV‐infected subjects – 99 on HAART (age range 23–57 years, mean 39 years) and 58 not on HAART (age range 20–59 years, mean 34 years) – and 50 non‐HIV controls (age range 19–59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV‐infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short‐term HAART (P < 0.01). The subjects with long‐term HAART were found to have a greater risk of having oral lesions than those with short‐term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05). Conclusion: We conclude that long‐term HAART has adverse effects on oral health status of HIV‐infected subjects. J Oral Pathol Med (2010) 39: 397-406Background: The aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy (HAART) on oral health status of HIV-infected subjects.Methods: Oral examination and measurement of saliva flow rate of both unstimulated and wax-stimulated whole saliva were performed in HIV-infected subjects with and without HAART, and in non-HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long-term use of HAART on oral health status of HIV-infected subjects.Results: One hundred and fifty-seven HIV-infected subjects - 99 on HAART (age range 23-57 years, mean 39 years) and 58 not on HAART (age range 20-59 years, mean 34 years) - and 50 non-HIV controls (age range 19-59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV-infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short-term HAART (P < 0.01). The subjects with long-term HAART were found to have a greater risk of having oral lesions than those with short-term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05).Conclusion: We conclude that long-term HAART has adverse effects on oral health status of HIV-infected subjects. The aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy (HAART) on oral health status of HIV-infected subjects. Oral examination and measurement of saliva flow rate of both unstimulated and wax-stimulated whole saliva were performed in HIV-infected subjects with and without HAART, and in non-HIV individuals. The following data were recorded; duration and risk of HIV infection, type and duration of HAART, CD4 cell count, viral load, presence of orofacial pain, oral dryness, oral burning sensation, oral lesions, cervical caries, and periodontal pocket. Multiple logistic regression analysis was performed to determine the effects of long-term use of HAART on oral health status of HIV-infected subjects. One hundred and fifty-seven HIV-infected subjects - 99 on HAART (age range 23-57 years, mean 39 years) and 58 not on HAART (age range 20-59 years, mean 34 years) - and 50 non-HIV controls (age range 19-59 years, mean 36 years) were enrolled. The most common HAART regimen was 2 NRTI + 2 NNRTI. HIV-infected subjects without HAART showed greater risks of having orofacial pain, oral dryness, oral lesions, and periodontal pockets than those with short-term HAART (P < 0.01). The subjects with long-term HAART were found to have a greater risk of having oral lesions than those with short-term HAART (P < 0.05). The unstimulated and stimulated salivary flow rates of the subjects with HAART were significantly lower than in those without HAART (P < 0.05). We conclude that long-term HAART has adverse effects on oral health status of HIV-infected subjects. |
Author | Nittayananta, Wipawee Silpapojakul, Kachornsakdi Talungchit, Sineepat Pruphetkaew, Nannapat Nilmanat, Ampaipith Chayakul, Panthip Jaruratanasirikul, Sutep |
AuthorAffiliation | 1 Epidemiology Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand 2 Department of Oral Surgery and Oral Medicine, Faculty of Dentistry, Srinakharinwirot University, Bangkok, Thailand 4 Division of Medicine, Hat Yai Regional Hospital, Hat Yai, Thailand 3 Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand |
AuthorAffiliation_xml | – name: 4 Division of Medicine, Hat Yai Regional Hospital, Hat Yai, Thailand – name: 2 Department of Oral Surgery and Oral Medicine, Faculty of Dentistry, Srinakharinwirot University, Bangkok, Thailand – name: 1 Epidemiology Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand – name: 3 Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand |
Author_xml | – sequence: 1 givenname: Wipawee surname: Nittayananta fullname: Nittayananta, Wipawee organization: Epidemiology Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand – sequence: 2 givenname: Sineepat surname: Talungchit fullname: Talungchit, Sineepat organization: Department of Oral Surgery and Oral Medicine, Faculty of Dentistry, Srinakharinwirot University, Bangkok, Thailand – sequence: 3 givenname: Sutep surname: Jaruratanasirikul fullname: Jaruratanasirikul, Sutep organization: Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand – sequence: 4 givenname: Kachornsakdi surname: Silpapojakul fullname: Silpapojakul, Kachornsakdi organization: Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand – sequence: 5 givenname: Panthip surname: Chayakul fullname: Chayakul, Panthip organization: Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand – sequence: 6 givenname: Ampaipith surname: Nilmanat fullname: Nilmanat, Ampaipith organization: Division of Medicine, Hat Yai Regional Hospital, Hat Yai, Thailand – sequence: 7 givenname: Nannapat surname: Pruphetkaew fullname: Pruphetkaew, Nannapat organization: Epidemiology Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20202089$$D View this record in MEDLINE/PubMed |
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References | Silvermann S Jr, Migliorati CA, Lozada-Nur F, Greenspan D, Conant MA. Oral findings in people with or at a high risk for AIDS; a study of 375 homosexual males. J Am Dent Assoc 1986; 112: 187-92. Greenspan D, Gange SJ, Phelan JA, et al. Incidence of oral lesions in HIV-1 infected women: reduction with HAART. J Dent Res 2004; 83: 145-50. Lin AL, Johnson DA, Stephan KT, Yeh CK. Alteration in salivary function in early HIV infection. J Dent Res 2003; 82: 719-24. Diz Dios P, Ocampo A, Miralles C, Otero I, Iglesias I, Rayo N. Frequency of oropharyngeal candidiasis in HIV-infected patients on protease inhibitor therapy. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999; 87: 437-41. Poizot-Martin I, Lafeuillade A, Dhiver C, et al. Cutaneo-mucosal hyperpigmentation in AIDS. 4 cases [in French]. Presse Med 1991; 20: 632-6. Phelan JA, Mulligan R, Nelson E, et al. Dental caries in HIV-seropositive women. J Dent Res 2004; 83: 869-73. Greenwood I, Zakrzewska JM, Robinson PG. 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Lancet 1998; 351: 252-5. Coates E, Slade GD, Goss AN, Gorkic E. Oral conditions and their social impact among HIV dental patients. Aust Dent J 1996; 41: 33-6. Baqui AA, Meiller T, Jabra-Rizk M, Zhang M, Kelley J, Falkler W. Association of HIV viral load with oral diseases. Oral Dis 1999; 5: 294-8. Lederman MM. Immune restoration and CD4+ T-cell function with antiretroviral therapies. AIDS 2001; 15(Suppl. 2): S11-5. Navazesh M, Mulligan R, Karim R, et al. Effect of HAART on salivary gland function in the Women's Interagency HIV Study (WIHS). Oral Dis 2009; 15: 52-60. Li TS, Tubiana R, Katlama C, Calvez V, Ait Mohand H, Autran B. Long-lasting recovery in CD4 T-cell function and viral-load reduction after highly active antiretroviral therapy in advanced HIV-1 disease. Lancet 1998; 351: 1682-6. Bretz WA, Flaitz C, Moretti A, Corby P, Schneider LG, Nichols CM. Medication usage and dental caries outcome-related variables in HIV/AIDS patients. AIDS Patient Care STDs 2000; 14: 549-54. Uccini S, D'Offizi G, Angelici A, et al. Cystic lymphoepithelial lesions of the parotid gland in HIV-1 infection. AIDS Patient Care STDs 2000; 14: 143-7. Coulter ID, Heslin KC, Marcus M, et al. Associations of self-reported oral health with physical and mental health in a nationally representative sample of HIV persons receiving medical care. Qual Life Res 2002; 11: 57-70. Bruner JM, Cleary KR, Smith FB, Batsakis JG. Immunocytochemical identification of HIV (p24) antigen in parotid lymphoid lesions. J Laryngol Otol 1989; 103: 1063-6. Kreimer AR, Alberg AJ, Daniel R, et al. Oral human papillomavirus infection in adults is associated with sexual behavior and HIV serostatus. J Infect Dis 2004; 189: 686-98. Nittayananta W, Chungpanich S. Oral lesions in a group of Thai people with AIDS. Oral Dis 1997; 3(Suppl. 1): 1-5. Miziara ID, Weber R. Oral lesions as predictors of highly active antiretroviral therapy failure in Brazilian HIV-infected children. J Oral Pathol Med 2008; 37: 99-106. Lin AL, Johnson DA, Sims CA, Stephan KT, Yeh CK. Salivary gland function in HIV-infected patients treated with highly active antiretroviral therapy (HAART). Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006; 102: 318-24. Ceballos-Salobrena A, Gaitan-Cepeda LA, Ceballos-Garcia L, Lezama-Del Valle D. Oral lesions in HIV/AIDS patients undergoing highly active antiretroviral treatment including protease inhibitors: a new face of oral AIDS? AIDS Patient Care STDS 2000; 14: 627-35. Nittayananta W, Chanowanna N, Jealae S, Nauntofte B, Stoltze K. Hyposalivation, xerostomia and oral health status of HIV-infected subjects in Thailand before HAART era. J Oral Pathol Med 2009 (in press). Schiodt M, Greenspan D, Daniels TE, et al. Parotid gland enlargement and xerostomia associated with labial sialadenitis in HIV-infected patients. J Autoimmun 1989; 2: 415-25. Laskaris G, Hadjivassiliou M, Stratigos J. Oral signs and symptoms in 160 Greek HIV-infected patients. J Oral Pathol Med 1992; 21: 120-3. Nicolatou-Galitis O, Velegraki A, Paikos S, et al. Effect of PI-HAART on the prevalence of oral lesions in HIV-I infected patients. A Greek study. Oral Dis 2004; 10: 145-50. Vicandi B, Jimenez-Heffernan JA, Lopez-Ferrer P, et al. HIV-1 (p24)-positive multinucleated giant cells in HIV-associated lymphoepithelial lesion of the parotid gland. A report of two cases. Acta Cytol 1999; 43: 247-51. Bendick C, Scheifele C, Reichart PA. Oral manifestations in 101 Cambodians with HIV and AIDS. J Oral Pathol Med 2002; 31: 1-4. Soberman N, Leonidas JC, Berdon WE, et al. Parotid enlargement in children seropositive for human immunodeficiency virus: imaging findings. AJR Am J Roentgenol 1991; 157: 553-6. Patton LL, McKaig R, Strauss R, Rogers D, Eron JJ Jr. Changing prevalence of oral manifestations of human immune-deficiency virus in the era of protease inhibitor therapy. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2000; 89: 299-304. Munro CA, Hube B. Anti-fungal therapy at the HAART of viral therapy. Trends Microbiol 2002; 10: 173-7. Navazesh M, Mulligan R, Barron Y, et al. A 4-year longitudinal evaluation of xerostomia and salivary gland hypofunction in the Women's Interagency HIV Study participants. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003; 95: 693-8. Tappuni AR, Fleming GJ. The effect of antiretroviral therapy on the prevalence of oral manifestations in HIV-infected patients: a UK study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2001; 92: 623-8. Arendorf TM, Bredekamp B, Cloete CA, Sauer G. Oral manifestations of HIV infection in 600 South African patients. J Oral Pathol Med 1998; 27: 176-9. Greenspan D, Canchola AJ, MacPhail LA, Cheikh B, Greenspan JS. Effect of highly active antiretroviral therapy on frequency of oral warts. Lancet 2001; 357: 1411-2. King MD, Reznik DA, O'Daniels CM, Larsen NM, Osterholt D, Blumberg HM. Human papillomavirus-associated oral warts among human immunodeficiency virus-seropositive patients in the era of highly active antiretroviral therapy: an emerging infection. Clin Infect Dis 2002; 34: 641-8. Nokta M. Oral manifestations associated with HIV infection. Curr HIV/AIDS Rep 2008; 5: 5-12. Itescu S, Brancato LJ, Buxbaum J, et al. A diffuse infiltrative CD8 lymphocytosis syndrome in human immunodeficiency virus (HIV) infection: a host immune response associated with HLA-DR5. Ann Intern Med 1990; 112: 3-10. Navazesh M, Mulligan R, Komaroff E, Redford M, Greenspan D, Phelan J. The prevalence of xerostomia and salivary gland hypofunction in a cohort of HIV-positive and at-risk women. J Dent Res 2000; 79: 1502-7. C'Decosta J, Saranath D, Dedhia P, Sanghvi V, Mehta AR. Detection of HPV-16 genome in human oral cancers and potentially malignant lesions from India. Oral Oncol 1998; 34: 413-20. Lorenz KA, Shapiro MF, Asch SM, Bozzette SA, Hays RD. 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References_xml | – reference: Li TS, Tubiana R, Katlama C, Calvez V, Ait Mohand H, Autran B. Long-lasting recovery in CD4 T-cell function and viral-load reduction after highly active antiretroviral therapy in advanced HIV-1 disease. Lancet 1998; 351: 1682-6. – reference: Cauda R, Tacconelli E, Tumbarello M, et al. Role of protease inhibitors in preventing recurrent oral candidosis in patients with HIV infection: a prospective case-control study. J Acquir Immune Defic Syndr 1999; 21: 20-5. – reference: Greenwood I, Zakrzewska JM, Robinson PG. Changes in the prevalence of HIV-associated mucosal disease at a dedicated clinic over 7 years. Oral Dis 2002; 8: 90-4. – reference: Bendick C, Scheifele C, Reichart PA. Oral manifestations in 101 Cambodians with HIV and AIDS. J Oral Pathol Med 2002; 31: 1-4. – reference: Poizot-Martin I, Lafeuillade A, Dhiver C, et al. Cutaneo-mucosal hyperpigmentation in AIDS. 4 cases [in French]. Presse Med 1991; 20: 632-6. – reference: Miziara ID, Weber R. Oral lesions as predictors of highly active antiretroviral therapy failure in Brazilian HIV-infected children. J Oral Pathol Med 2008; 37: 99-106. – reference: Navazesh M, Mulligan R, Karim R, et al. Effect of HAART on salivary gland function in the Women's Interagency HIV Study (WIHS). Oral Dis 2009; 15: 52-60. – reference: Silvermann S Jr, Migliorati CA, Lozada-Nur F, Greenspan D, Conant MA. Oral findings in people with or at a high risk for AIDS; a study of 375 homosexual males. J Am Dent Assoc 1986; 112: 187-92. – reference: Sharma G, Pai KM, Suhas S, Ramapuram JT, Doshi D, Anup N. Oral manifestations in HIV/AIDS infected patients from India. Oral Dis 2006; 12: 537-42. – reference: Greenberg RG, Berger TG. Nail and mucocutaneous hyperpigmentation with azidothymidine therapy. J Am Acad Dermatol 1990; 22: 327-30. – reference: Bruner JM, Cleary KR, Smith FB, Batsakis JG. Immunocytochemical identification of HIV (p24) antigen in parotid lymphoid lesions. 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Oral Dis 2004; 10: 145-50. – reference: Laskaris G, Hadjivassiliou M, Stratigos J. Oral signs and symptoms in 160 Greek HIV-infected patients. J Oral Pathol Med 1992; 21: 120-3. – reference: Itescu S, Brancato LJ, Buxbaum J, et al. A diffuse infiltrative CD8 lymphocytosis syndrome in human immunodeficiency virus (HIV) infection: a host immune response associated with HLA-DR5. Ann Intern Med 1990; 112: 3-10. – reference: Ramirez-Amador V, Esquivel-Pedraza L, Sierra-Madero J, Anaya-Saavedra G, Gonzalez-Ramirez L, Ponce-de-Leon S. The changing clinical spectrum of human immunodeficiency virus (HIV)-related oral lesions in 1000 consecutive patients: a 12-year study in a referral center in Mexico. Medicine (Baltimore) 2003; 82: 39-50. – reference: Soberman N, Leonidas JC, Berdon WE, et al. Parotid enlargement in children seropositive for human immunodeficiency virus: imaging findings. 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Antiretroviral therapy with protease inhibitors has an early, immune reconstitution-independent beneficial effect on Candida virulence and oral candidiasis in human immunodeficiency virus-infected subjects. J Infect Dis 2002; 185: 188-95. – reference: Greenspan D, Canchola AJ, MacPhail LA, Cheikh B, Greenspan JS. Effect of highly active antiretroviral therapy on frequency of oral warts. Lancet 2001; 357: 1411-2. – reference: King MD, Reznik DA, O'Daniels CM, Larsen NM, Osterholt D, Blumberg HM. Human papillomavirus-associated oral warts among human immunodeficiency virus-seropositive patients in the era of highly active antiretroviral therapy: an emerging infection. Clin Infect Dis 2002; 34: 641-8. – reference: Phelan JA, Mulligan R, Nelson E, et al. Dental caries in HIV-seropositive women. J Dent Res 2004; 83: 869-73. – reference: Patton LL, Strauss RP, McKaig RG, Porter DR, Eron JJ Jr. Perceived oral health status, unmet needs, and barriers to dental care among HIV/AIDS patients in a North Carolina cohort: impacts of race. J Public Health Dent 2003; 63: 86-91. – reference: Tukutuku K, Muyembe-Tamfum L, Kayembe K, Odio W, Kandi K, Ntumba M. Oral manifestations of AIDS in a heterosexual population in a Zaire hospital. J Oral Pathol Med 1990; 19: 232-4. – reference: Powderly WG, Landay A, Lederman MM. Recovery of the immune system with antiretroviral therapy: the end of opportunism? J Am Med Assoc 1998; 280: 72-7. – reference: Baqui AA, Meiller T, Jabra-Rizk M, Zhang M, Kelley J, Falkler W. Association of HIV viral load with oral diseases. Oral Dis 1999; 5: 294-8. – reference: Lin AL, Johnson DA, Sims CA, Stephan KT, Yeh CK. Salivary gland function in HIV-infected patients treated with highly active antiretroviral therapy (HAART). Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006; 102: 318-24. – reference: Navazesh M, Mulligan R, Barron Y, et al. A 4-year longitudinal evaluation of xerostomia and salivary gland hypofunction in the Women's Interagency HIV Study participants. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003; 95: 693-8. – reference: Tappuni AR, Fleming GJ. The effect of antiretroviral therapy on the prevalence of oral manifestations in HIV-infected patients: a UK study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2001; 92: 623-8. – reference: Race EM, Adelson-Mitty J, Kriegel GR, et al. Focal mycobacterial lymphadenitis following initiation of protease-inhibitor therapy in patients with advanced HIV-1 disease. Lancet 1998; 351: 252-5. – reference: Nokta M. Oral manifestations associated with HIV infection. Curr HIV/AIDS Rep 2008; 5: 5-12. – reference: Scully C, Diz Dios P. Orofacial effects of antiretroviral therapies. 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Snippet | J Oral Pathol Med (2010) 39: 397–406
Background: The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy... J Oral Pathol Med (2010) 39 : 397–406 Background: The aim of this study was to determine the effects of long‐term use of highly active antiretroviral therapy... The aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy (HAART) on oral health status of HIV-infected... J Oral Pathol Med (2010) 39: 397-406Background: The aim of this study was to determine the effects of long-term use of highly active antiretroviral therapy... |
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SubjectTerms | Adult Age Antiretroviral Therapy, Highly Active - adverse effects Burning Case-Control Studies CD4 antigen Cross-Sectional Studies Data processing Dental caries Dental Caries - complications Female HAART Health Status highly active antiretroviral therapy HIV HIV Infections - complications HIV Infections - drug therapy Human immunodeficiency virus Humans Infection Linear Models Logistic Models Male Middle Aged Mouth Diseases - complications Oral Health oral lesion Pain Periodontal Index Pigmentation Disorders - etiology Regression analysis risk factor Saliva salivary flow rate Salivation - drug effects Secretory Rate Side effects Thailand Time Factors Young Adult |
Title | Effects of long-term use of HAART on oral health status of HIV-infected subjects |
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