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 inJournal of oral pathology & medicine Vol. 39; no. 5; pp. 397 - 406
Main Authors Nittayananta, Wipawee, Talungchit, Sineepat, Jaruratanasirikul, Sutep, Silpapojakul, Kachornsakdi, Chayakul, Panthip, Nilmanat, Ampaipith, Pruphetkaew, Nannapat
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.05.2010
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ISSN0904-2512
1600-0714
1600-0714
DOI10.1111/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.
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
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  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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2010 John Wiley & Sons A/S · All rights reserved 2010
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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.
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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.
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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.
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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.
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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.
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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.
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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. J Laryngol Otol 1989; 103: 1063-6.
– reference: Lederman MM. Immune restoration and CD4+ T-cell function with antiretroviral therapies. AIDS 2001; 15(Suppl. 2): S11-5.
– reference: Ho DD. Time to hit HIV, early and hard. N Engl J Med 1995; 333: 450-1.
– reference: Lin AL, Johnson DA, Stephan KT, Yeh CK. Alteration in salivary function in early HIV infection. J Dent Res 2003; 82: 719-24.
– reference: Olive A, Salavert A, Manriquez M, Clotet B, Moragas A. Parotid lipomatosis in HIV positive patients: a new clinical disorder associated with protease inhibitors. Ann Rheum Dis 1998; 57: 749.
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– reference: 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.
– reference: 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.
– reference: 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.
– reference: EC-Clearinghouse on Oral Problems Related to HIV Infection and WHO Collaborating Centre on Oral Manifestations of the Human Immunodeficiency Virus. Classification and diagnostic criteria for oral lesions in HIV infection. J Oral Pathol Med 1993; 22: 289-91.
– reference: 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.
– reference: 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.
– reference: 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.
– reference: Munro CA, Hube B. Anti-fungal therapy at the HAART of viral therapy. Trends Microbiol 2002; 10: 173-7.
– reference: Silverberg MJ, Gore ME, French AL, et al. Prevalence of clinical symptoms associated with highly active antiretroviral therapy in the Women's Interagency HIV Study. Clin Infect Dis 2004; 39: 717-24.
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– reference: 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.
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– reference: 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.
– reference: Ramos-Gomez FJ, Flaitz C, Catapano P, Murray P, Milnes AR, Dorenbaum A. Classification, diagnostic criteria, and treatment recommendations for orofacial manifestations in HIV-infected pediatric patients. Collaborative Workgroup on Oral Manifestations of Pediatric HIV Infection. J Clin Pediatr Dent 1999; 23: 85-96.
– reference: 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.
– reference: 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.
– reference: Chasombat S, McConnell MS, Siangphoe U, et al. National expansion of antiretroviral treatment in Thailand, 2000-2007: program scale-up and patient outcomes. J Acquir Immune Defic Syndr 2009; 50: 506-12.
– reference: 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.
– 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.
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– reference: 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).
– reference: Ramirez V, Gonzalez A, De La Rosa E, et al. Oral lesions in Mexican HIV-infected patients. J Oral Pathol Med 1990; 19: 482-5.
– reference: Schmidt-Westhausen AM, Priepke F, Bergmann FJ, Reichart PA. Decline in the rate of oral opportunistic infections following introduction of highly active antiretroviral therapy. J Oral Pathol Med 2000; 29: 336-41.
– reference: 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.
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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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StartPage 397
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
URI https://api.istex.fr/ark:/67375/WNG-B0T8RM4K-S/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1600-0714.2009.00875.x
https://www.ncbi.nlm.nih.gov/pubmed/20202089
https://www.proquest.com/docview/733282498
https://www.proquest.com/docview/744697278
https://pubmed.ncbi.nlm.nih.gov/PMC3217232
Volume 39
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