Abstract
Purpose of Review
With the establishment of antiretroviral treatment (ART) programs in low- and middle-income countries, people with HIV (PWH) in Latin America and the Caribbean (LAC) are living longer, subsequently developing chronic non-communicable diseases (NCDs). Few studies focus on the impact of aging among older LAC PWH. This systematic review aims to fill this information gap and understand the burden of aging with HIV in LAC. We identified peer-reviewed literature published in English, Spanish, or Portuguese from several databases to assess currently available evidence on the burden of aging with HIV in LAC and selected six common NCDs found in older PWH (cardiovascular disease [CVD], bone and musculoskeletal [MSK] disorders, cancer, renal disease, neurocognitive impairment [NCI], and depression).
Recent Findings
Of the 5942 publications reviewed, only 53 articles were found with populations 40 years and older or age-related findings (27 CVD, 13 NCI or depression, 6 MSK disorders, 4 renal disease, 3 cancer). Most (79%) publications were from Brazil with few longitudinal studies on aging with HIV. Prevalence of illnesses such as CVD, NCI, depression, or osteoporosis varied widely depending on the screening instrument utilized and geographic population surveyed. Age was a significant predictor of comorbidity in nearly all studies.
Summary
Our results demonstrate the need for longitudinal studies and validated screening instruments appropriate for use among PWH in LAC. Understanding the mechanisms behind aging in HIV and the roles of sociocultural factors and genetic diversity specific to LAC is needed to appropriately manage chronic comorbidities as PWH age.
Similar content being viewed by others
References
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
Shao Y, Williamson C. The HIV-1 epidemic: low- to middle-income countries. Cold Spring Harb Perspect Med. 2012;2(3). https://doi.org/10.1101/cshperspect.a007187.
Patel P, Rose CE, Collins PY, Nuche-Berenguer B, Sahasrabuddhe VV, Peprah E, et al. Noncommunicable diseases among HIV-infected persons in low-income and middle-income countries: a systematic review and meta-analysis. AIDS. 2018;32(Suppl 1):S5–S20. https://doi.org/10.1097/QAD.0000000000001888.
Latin America and the Caribbean. UNAIDS. Published 2019. https://www.unaids.org/en/regionscountries/latinamerica. Accessed July 17, 2020.
García PJ, Bayer A, Cárcamo CP. The changing face of HIV in Latin America and the Caribbean. Curr HIV/AIDS Rep. 2014;11(2):146–57. https://doi.org/10.1007/s11904-014-0204-1.
Rezende EL, Vasconcelos AM, Pereira MG. Causes of death among people living with HIV/AIDS in Brazil. Braz J Infect Dis. 2010;14(6):558–63.
Pacheco AGF. CHANGES IN CAUSES OF DEATH IN HIV/AIDS patients in brazil in the HAART era. :103.
Crabtree-Ramirez B, Del Rio C, Grinsztejn B, Sierra-Madero J. HIV and noncommunicable diseases (NCDs) in Latin America: a call for an integrated and comprehensive response. J Acquir Immune Defic Syndr. 2014;67(SUPPL.1):S96–8. https://doi.org/10.1097/QAI.0000000000000261.
Brites C, Nogueira RS, Gosuen GC, Kalmar EMC, Leme STS, Martins RT, et al. Short communication: getting older with HIV: increasing frequency of comorbidities and polypharmacy in Brazilian HIV patients. AIDS Res Hum Retrovir. 2019;35(11–12):1103–5. https://doi.org/10.1089/AID.2019.0069.
Alonso Gonzalez M, Martin L, Munoz S, Jacobson JO. Patterns, trends and sex differences in HIV/AIDS reported mortality in Latin American countries: 1996-2007. BMC Public Health. 2011;11(1):605. https://doi.org/10.1186/1471-2458-11-605.
Calderón S. Perfil epidemiológico de los pacientes adultos mayores de 60 años de la clínica de VIH/SIda del hospital calderón guardia, del 01 enerero 2005 al 30 de septiembre de 2014. Published online 2015.
Torres TS, Cardoso SW, Velasque Lde S, et al. Aging with HIV: an overview of an urban cohort in Rio de Janeiro (Brazil) across decades of life. Braz J Infect Dis. 2013;17(3):324–31. https://doi.org/10.1016/j.bjid.2012.10.024.
Ramirez N. Caracteristicas clínicas y epidemiológicas de la infeccion por vih en pacientes mayores de 50 años. Ciudad Hospitoaliaria “Dr. Enrique Tejera” 2005-2015. Published online 2015.
Corréa PP. Perfil Clíinico e epidemiológico de individuos com 50 anos ou mais com HIV/AIDS acompanhados no ambulatório de doencas infecciosas e parasitárias de um hospital universitario em Niterói, RJ. Published online 2016.
Oliveira DAD. Envejeciento com VIH: história de lutas e desafios. Published online. 2013;127.
Calazans JA, Queiroz BL. The adult mortality profile by cause of death in 10 Latin American countries (2000–2016). Rev Panam Salud Pública. 2020;44:1. https://doi.org/10.26633/RPSP.2020.1.
Akl LD, Valadares ALR, de Moraes MJ, Pinto-Neto AM, Lagrutta B, Costa-Paiva L. Metabolic syndrome in HIV-infected middle-aged women on antiretroviral therapy: prevalence and associated factors. Braz J Infect Dis. 2017;21(3):263–9. https://doi.org/10.1016/j.bjid.2017.02.003.
Diehl LA, Dias JR, Paes ACS, Thomazini MC, Garcia LR, Cinagawa E, et al. Prevalência da lipodistrofia associada ao HIV em pacientes ambulatoriais brasileiros: relação com síndrome metabólica e fatores de risco cardiovascular. Arq Bras Endocrinol Metab. 2008;52(4):658–67. https://doi.org/10.1590/S0004-27302008000400012.
Antinori A, Arendt G, Becker JT, Brew BJ, Byrd DA, Cherner M, et al. Updated research nosology for HIV-associated neurocognitive disorders. Neurology. 2007;69(18):1789–99. https://doi.org/10.1212/01.WNL.0000287431.88658.8b.
McArthur JC. HIV dementia: an evolving disease. J Neuroimmunol. 2004;157(1–2):3–10. https://doi.org/10.1016/j.jneuroim.2004.08.042.
Sacktor N, Saylor D, Nakigozi G, Nakasujja N, Robertson K, Grabowski MK, et al. Effect of HIV subtype and antiretroviral therapy on HIV-associated neurocognitive disorder stage in Rakai, Uganda. J Acquired Immune Defic Syndr. 2019;81(2):216–23. https://doi.org/10.1097/QAI.0000000000001992.
Saloner R, Cysique LA. HIV-associated neurocognitive disorders: a global perspective. J Int Neuropsychol Soc. 2017;23(9–10):860–9. https://doi.org/10.1017/S1355617717001102.
Heaton RK, Clifford DB, Franklin DR, Woods SP, Ake C, Vaida F, et al. HIV-associated neurocognitive disorders persist in the era of potent antiretroviral therapy: CHARTER Study. Neurology. 2010;75(23):2087–96. https://doi.org/10.1212/WNL.0b013e318200d727.
Tebas P, Powderly WG, Claxton S, et al. Accelerated bone mineral loss in HIV-infected patients receiving potent antiretroviral therapy. AIDS. 2000;14(4):F63–7. https://doi.org/10.1097/00002030-200003100-00005.
Hansen A-BE, Gerstoft J, Kronborg G, Larsen CS, Pedersen C, Pedersen G, et al. Incidence of low and high-energy fractures in persons with and without HIV infection: a Danish population-based cohort study. AIDS. 2012;26(3):285–93. https://doi.org/10.1097/QAD.0b013e32834ed8a7.
Menezes AM, Torelly J, Barbi C, Camargo CC, Moraes RP, Sprinz E. Mild decrease in renal function in HIV-infected patients on antiretroviral therapy: a neglected diagnosis. J AIDS Clin Res. 2015;6(9). http://www.omicsonline.org/open-access/mild-decrease-in-renal-function-in-hivinfected-patients-on-antiretroviral-therapy-a-neglected-diagnosis-2155-6113-1000501.php?aid=60697, http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=cagh&AN=2015.
Nguyen ML, Farrell K, Gunthel C. Non-AIDS-defining malignancies in patients with HIV in the HAART era. Curr Infect Dis Rep. 2010;12:46–55. https://doi.org/10.1007/s11908-009-0075-6.
Silva MM da, Vasconcelos ALR de, Ribeiro LK de NP. Caracterização epidemiológica dos casos de AIDS em pessoas com 60 anos ou mais, Pernambuco, Brasil, 1998 a 2008. Cad Saúde Pública 2013;29(10):2131–2135. https://doi.org/10.1590/0102-311X00161112.
Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336–41. https://doi.org/10.1016/j.ijsu.2010.02.007.
McGowan J, Sampson M, Salzwedel DM, Cogo E, Foerster V, Lefebvre C. PRESS peer review of electronic search strategies: 2015 guideline statement. J Clin Epidemiol. 2016;75:40–6. https://doi.org/10.1016/j.jclinepi.2016.01.021.
Barros ZM, de Alencar Ximenes RA, Miranda-Filho DB, de Albuquerque MFPM, Melo HRL, Carvalho ÉH, et al. Comparison between the Framingham and prospective cardiovascular of Münster scores for risk assessment of coronary heart disease in human immunodeficiency virus–positive patients in Pernambuco, Brazil. Metab Syndr Relat Disord. 2010;8(6):489–97. https://doi.org/10.1089/met.2009.0100.
Fuchs SC, Alencastro PR, Ikeda MLR, Barcellos NT, Wolff FH, Brandão ABM, et al. Risk of coronary heart disease among HIV-infected patients: a multicenter study in Brazil. Sci World J. 2013;2013:1–8. https://doi.org/10.1155/2013/163418.
Pinto Neto LF, da S, Dias FR, Bressan FF, Santos CRO. Comparison of the ACC/AHA and Framingham algorithms to assess cardiovascular risk in HIV-infected patients. Braz J Infect Dis. 2017;21(6):577–80. https://doi.org/10.1016/j.bjid.2017.06.007.
Fonseca Pacheco AG. Changes in causes of death in HIV/AIDS patients in Brazil in the HAART era. Dissertation Abstracts International: Section B: The Sciences and Engineering. 2009;69(11-B). http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=psyc6&AN=2009-99100-276, http://wa4py6yj8t.search.serialssolutions.com/?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rfr_id=info:sid/Ovid:psyc6&rft.genre=article&rft_id=inf.
Maciel RA, Kluck HM, Durand M, Sprinz E. Comorbidity is more common and occurs earlier in persons living with HIV than in HIV-uninfected matched controls, aged 50 years and older: a cross-sectional study. Int J Infect Dis. 2018;70:30–5. https://doi.org/10.1016/j.ijid.2018.02.009.
Castilho JL, Escuder MM, Veloso V, Gomes JO, Jayathilake K, Ribeiro S, et al. Trends and predictors of non-communicable disease multimorbidity among adults living with HIV and receiving antiretroviral therapy in Brazil. J Int AIDS Soc. 2019;22(1):e25233. https://doi.org/10.1002/jia2.25233.
Brites-Alves C, Luz E, Netto EM, Ferreira T, Diaz RS, Pedroso C, et al. Immune activation, proinflammatory cytokines, and conventional risks for cardiovascular disease in HIV patients: a case-control study in Bahia, Brazil. Front Immunol. 2018;9:1469. https://doi.org/10.3389/fimmu.2018.01469.
Lister-Del Pino P, León-Amenero G, Leiva-Montejo A, Segura ER. Concordancia entre las escalas de riesgo cardiovascular PROCAM y FRAMINGHAM en varones que reciben tratamiento antirretroviral en un hospital nacional de Lima, Perú 2013. Rev Peru Med Exp Salud Publica. 2015;32(4):731. https://doi.org/10.17843/rpmesp.2015.324.1765.
Cahn P, Leite O, Rosales A, et al. Metabolic profile and cardiovascular risk factors among Latin American HIV-infected patients receiving HAART. Braz J Infect Dis. 9.
de Araújo PSR, de Alencar Ximenes RA, Lopes CFC, Duarte JY, da Silva MM, Carneiro EM. Antiretroviral treatment for HIV infection/AIDS and the risk of developing hyperglycemia and hyperlipidemia. Rev Inst Med trop S Paulo. 2007;49(2):73–8. https://doi.org/10.1590/S0036-46652007000200002.
Farhi L, de Lima DB, Cunha CB. Dislipidemia em pacientes HIV/AIDS em uso de anti-retrovirais num hospital universitário, Rio de Janeiro, Brasil. J Bras Patol Med Lab. 2008;44(3). https://doi.org/10.1590/S1676-24442008000300004.
Melo ES, Costa CRB, Foresto JS, Antonini M, Pontes PS, Reis RK. Análisis de la dislipidemia en adultos que viven con VIH. Rev Cuid. 2019;10(2). https://doi.org/10.15649/cuidarte.v10i2.776.
da Conceição Brandão de Arruda Falcão M, Zírpoli JC, de Albuquerque VM, et al. Association of biomarkers with atherosclerosis and risk for coronary artery disease in patients with HIV. Arq Bras Cardiol. 2012;99(5):971–8. https://doi.org/10.1590/s0066-782x2012005000093.
Pacheco AG, Grinsztejn B, Fonseca M de JM da, et al. HIV infection is not associated with carotid intima-media thickness in brazil: a cross-sectional analysis from the INI/ELSA-Brasil study. De Socio GV, ed. PLoS ONE. 2016;11(7):e0158999. https://doi.org/10.1371/journal.pone.0158999.
Pinto Neto LF, da S, das Neves MB, Ribeiro-Rodrigues R, Page K, Miranda AE. Dyslipidemia and fasting glucose impairment among HIV patients three years after the first antiretroviral regimen in a Brazilian AIDS outpatient clinic. Braz J Infect Dis. 2013;17(4):438–43. https://doi.org/10.1016/j.bjid.2012.12.006.
de Carvalho ÉH, Filho D, de BM, de Alencar Ximenes RA, et al. Prevalence of hyperapolipoprotein B and associations with other cardiovascular risk factors among human immunodeficiency virus–infected patients in Pernambuco, Brazil. Metab Syndr Relat Disord. 2010;8(5):403–10. https://doi.org/10.1089/met.2009.0092.
Mata-Marin JA. Dyslipidemia and fasting glucose impairment among HIV-infected patients 48-weeks after the first antiretroviral regimen. J AIDS Clin Res. 2015;06(12). https://doi.org/10.4172/2155-6113.1000533.
Mata-Marin JA, Martinez-Osio MH, Arroyo-Anduiza CI, et al. Comorbidities and polypharmacy among HIV-positive patients aged 50 years and over: a case-control study. BMC Res Notes. 2019;12(1):556. https://doi.org/10.1186/s13104-019-4576-6.
Rondan PL, Flores-Flores O, Doria NA, Valencia-Mesias G, Chávez-Pérez V, Soria J. Elevada frecuencia de dislipidemia en pacientes infectados por VIH en un hospital público peruano. Rev Peru Med Exp Salud Publica. 2017;34(2):239. https://doi.org/10.17843/rpmesp.2017.342.2587.
Hidalgo JA, Florez A, Agurto C, Pinedo Y, Ayarza R, Rodriguez L, et al. Metabolic and cardiovascular comorbidities among clinically stable HIV patients on long-term ARV therapy in five ambulatory clinics in Lima-Callao, Peru. TOAIDJ. 2018;12(1):126–35. https://doi.org/10.2174/1874613601812010126.
Lacerda HR, da Conceição Correia Falcão M, de Albuquerque VMG, et al. Association of inflammatory cytokines and endothelial adhesion molecules with immunological, virological, and cardiometabolic disease in HIV-infected individuals. J Interf Cytokine Res. 2014;34(5):385–93. https://doi.org/10.1089/jir.2013.0029.
Alvarez C, Salazar R, Galindez J, Rangel F, Castañeda ML, Lopardo G, et al. Metabolic syndrome in HIV-infected patients receiving antiretroviral therapy in Latin America. Braz J Infect Dis. 2010;14(3):256–63. https://doi.org/10.1016/S1413-8670(10)70053-2.
de Arruda Junior ER, Lacerda HR, Moura LCRV, et al. Risk factors related to hypertension among patients in a cohort living with HIV/AIDS. Braz J Infect Dis. 2010;14(3):281–7. https://doi.org/10.1590/s1413-86702010000300014.
de Arruda Júnior ER, Lacerda HR, Moura LCRV, et al. Profile of patients with hypertension included in a cohort with HIV/AIDS in the state of Pernambuco, Brazil. Arq Bras Cardiol. 2010;95(5):640–7. https://doi.org/10.1590/s0066-782x2010005000138.
da Cunha GH, Lima MAC, Galvão MTG, Fechine FV, Fontenele MSM, Siqueira LR. Prevalence of arterial hypertension and risk factors among people with acquired immunodeficiency syndrome. Rev Lat Am Enfermagem. 2018;26:e3066. https://doi.org/10.1590/1518-8345.2684.3066.
Sereia AL, Junior MS, Domiciano TP, Shimauti E, Pupulin ART. Mini Mental State Examination and evaluation of factors associated with cognitive decline in HIV/AIDS-infected people. Acta Sci Health Sci. 2012;34(2):193–8. https://doi.org/10.4025/actascihealthsci.v34i2.12687.
Araujo ML de Duarte W, de Oliveira ACP, et al. Is the telomere length associated with neurocognitive disabilities in HIV-1-infected subjects? Revista do Instituto de Medicina Tropical de Sao Paulo. 2018;60(38). http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0036-46652018005000207&lng=en&nrm=iso&tlng=en, http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=cagh&AN=20193122783, http://wa4py6yj8t.search.serialssolutions.com/?url_ver=Z39.88-2004.
Pinheiro CAT, Souza LDM, Motta JVS, Kelbert EF, Souza MS, Martins CSR, et al. Depression and diagnosis of neurocognitive impairment in HIV-positive patients. Braz J Med Biol Res. 2016;49(10):e5344. https://doi.org/10.1590/1414-431x20165344.
Pinheiro CAT, de Mattos Souza LD, Dos Santos Motta JV, et al. Aging, neurocognitive impairment and adherence to antiretroviral therapy in human immunodeficiency virus-infected individuals. Braz J Infect Dis. 2016;20(6):599–604. https://doi.org/10.1016/j.bjid.2016.09.006.
Troncoso FT, de Oliveira Conterno L. Prevalence of neurocognitive disorders and depression in a Brazilian HIV population. Rev Soc Bras Med Trop. 2015;48(4):390–8. https://doi.org/10.1590/0037-8682-0034-2015.
Filho SMMF, de Melo HRL. Frequency and risk factors for HIV-associated neurocognitive disorder and depression in older individuals with HIV in northeastern Brazil. Int Psychogeriatr. 2012;24(10):1648–55. https://doi.org/10.1017/S1041610212000944.
Gascon MRP, Vidal JE, Mazzaro YM, et al. Neuropsychological assessment of 412 HIV-infected individuals in Sao Paulo, Brazil. AIDS Patient Care STDS. 2018;32(1):1–8. https://doi.org/10.1089/apc.2017.0202.
Zamudio-Rodríguez A, Belaunzaran-Zamudio PF, Sierra-Madero JG, et al. Association between frailty and HIV-associated neurodegenerative disorders among older adults living with HIV. AIDS Res Hum Retrovir. 2018;34(5):449–55. https://doi.org/10.1089/AID.2017.0100This study investigated the relationship between frailty and HIV-associated neurodegenerative disorder among older people with HIV, and was the only study to determine the relationship between frailty and pre-frailty, known to be common in aging in HIV, and cognitive impairment of all studies we identified.
do Carmo Filho A, Fakoury MK, de Araujo Eyer-Silva W, Neves-Motta R, Kalil RS, de Almeida Ferry FR. Factors associated with a diagnosis of major depression among HIV-infected elderly patients. Rev Soc Bras Med Trop. 2013;46(3):352–4. https://doi.org/10.1590/0037-8682-1228-2013.
Avila-Funes JA, Zamudio-Rodríguez A, Muñoz-Nevárez LA, Belaunzarán-Zamudio PF, Díaz-Ramos JA, Alcala-Zermeno JL, et al. Correlates of depressive symptoms among older adults living with HIV. Int J Geriatr Psychiatry. 2018;33(9):1260–4. https://doi.org/10.1002/gps.4922.
Chaba D, Soares LR, Pereira RMR, et al. Low bone mineral density among HIV-infected patients in Brazil. Rev Inst Med Trop Sao Paulo. 2017;59:e89. https://doi.org/10.1590/S1678-9946201759089.
Gomes DC, Valadares AL, Amaral E, et al. Association between HIV infection and bone mineral density in climacteric women. Arch Osteoporos. 2015;10:33. https://doi.org/10.1007/s11657-015-0238-z.
Pinto Neto LF, Ragi-Eis S, Vieira NF, et al. Low bone mass prevalence, therapy type, and clinical risk factors in an HIV-infected Brazilian population. J Clin Densitom. 2011;14(4):434–9. https://doi.org/10.1016/j.jocd.2011.06.004.
Pinto Neto LF, Sales MC, Scaramussa ES, da Paz CJ, Morelato RL. Human immunodeficiency virus infection and its association with sarcopenia. Braz J Infect Dis. 2016;20(1):99–102. https://doi.org/10.1016/j.bjid.2015.10.003.
Perez C, Ceballos ME. High frequency of hypovitaminosis D and low bone mineral density in a sample of HIV-infected men in Chile. Rev Chil Infectol. 2014;31(1):44–6. https://doi.org/10.4067/S0716-10182014000100006.
Mata-Marin JA, Arroyo-Anduiza CI, Berrospe-Silva MLA, Chaparro-Sanchez A, Gil-Avila A, Gaytan-Martinez J. Mexican patients with HIV have a high prevalence of vertebral fractures. Infect Dis Reports. 2018;10(1):7409. https://doi.org/10.4081/idr.2018.7409This was the only study that assessed osteoporotic vertebral fractures throughout all the Latin American and the Caribbean region, showing important findings in terms of prevalence and risk factors among HIV-infected populations.
Pereira AC, Bradbury F, Rossetti ES, Hortense P. Avaliação da dor e fatores associados em pessoas que vivem com HIV/AIDS. Rev Lat Am Enfermagem. 2019;27:e3155. https://doi.org/10.1590/1518-8345.2803.3155.
Avila-Funes JA, Belaunzaran-Zamudio PF, Tamez-Rivera O, et al. Correlates of prevalent disability among HIV-infected elderly patients. AIDS Res Hum Retrovir. 2016;32(2):155–62. https://doi.org/10.1089/aid.2015.0171.
Zeballos D, Lins L, Brites C. Frailty and its association with health related quality of life in older HIV patients, in Salvador, Brazil. AIDS Res Hum Retrovir. 2019;35(11–12):1074–81. https://doi.org/10.1089/aid.2019.0103.
Santiago P, Grinsztejn B, Friedman RK, et al. Screening for decreased glomerular filtration rate and associated risk factors in a cohort of HIV-infected patients in a middle-income country. PLoS ONE. 2014;9(4). https://doi.org/10.1371/journal.pone.0093748.
Pinto Neto LFS, Braga AC, Rocha JA, Vieira NFR, Miranda AE. Risk factors related to renal disorders in HIV-1 infected patients. Rev Soc Bras Med Trop. 2011;44(1):30–4. https://doi.org/10.1590/S0037-86822011000100008.
Antonello V, Antonello I, Herrmann S, Tovo C. Proteinuria is common among HIV patients: what are we missing? Clinics. 2015;70(10):691–5. https://doi.org/10.6061/clinics/2015(10)06.
Andrade AC, Luz PM, Veloso VG, et al. Breast cancer in a cohort of human immunodeficiency virus (HIV)-infected women from Rio de Janeiro, Brazil: a cases series report and an incidence rate estimate. Braz J Infect Dis. 2011;15(4):387–93.
da Silva Pinto Neto LF, da Conceição Milanez M, Golub JE, Miranda AEB. Malignancies in HIV/AIDS patients attending an outpatient clinic in Vitória, State of Espírito Santo, Brazil. Rev Soc Bras Med Trop. 2012;45(6):687–90. https://doi.org/10.1590/S0037-86822012000600006.
Ferreira MP, Coghill AE, Chaves CB, Bergmann A, Thuler LC, Soares EA, et al. Outcomes of cervical cancer among HIV-infected and HIV-uninfected women treated at the Brazilian National Institute of Cancer. AIDS. 2017;31(4):523–31. https://doi.org/10.1097/QAD.0000000000001367.
the AIDS Clinical Trials Group, Robertson K, Kumwenda J, et al. A multinational study of neurological performance in antiretroviral therapy-naïve HIV-1-infected persons in diverse resource-constrained settings. J Neuro-Oncol. 2011;17(5):438–47. https://doi.org/10.1007/s13365-011-0044-3.
Power C, Selnes OA, Grim JA, McArthur JC. HIV dementia scale: a rapid screening test. J Acquir Immune Defic Syndr Hum Retrovirol. 1995;8(3):273–8. https://doi.org/10.1097/00042560-199503010-00008.
Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12(3):189–98. https://doi.org/10.1016/0022-3956(75)90026-6.
Lewiecki EM. Osteoporosis: clinical evaluation. In: Feingold KR, Anawalt B, Boyce A, et al., eds. Endotext. MDText.com, Inc.; 2000. http://www.ncbi.nlm.nih.gov/books/NBK279049/. Accessed July 19, 2020.
Ilha TASH, Comim FV, Copes RM, Compston JE, Premaor MO. HIV and vertebral fractures: a systematic review and metanalysis. Sci Rep. 2018;8(1):7838. https://doi.org/10.1038/s41598-018-26312-9.
Moreira VG, Lourenço RA. Prevalence and factors associated with frailty in an older population from the city of Rio de Janeiro, Brazil: the FIBRA-RJ Study. Clinics (Sao Paulo). 2013;68(7):979–85. https://doi.org/10.6061/clinics/2013(07)15.
Pinto Neto LF, Milanez Mda C, Golub JE, Miranda AE. Malignancies in HIV/AIDS patients attending an outpatient clinic in Vitoria, State of Espirito Santo, Brazil. Rev Soc Bras Med Trop. 2012;45(6):687–90.
Belaunzaran-Zamudio PF, Caro-Vega Y, Giganti MJ, et al. Frequency of non-communicable diseases in people 50 years of age and older receiving HIV care in Latin America. Nunes BP, ed. PLoS ONE. 2020;15(6):e0233965. https://doi.org/10.1371/journal.pone.0233965.
Caro-Vega Y, Belaunzarán-Zamudio PF, Crabtree-Ramírez B, Shepherd BE, Mejia F, Giganti MJ, et al. Trends in proportion of older HIV-infected people in care in Latin America and the Caribbean: a growing challenge. Epidemiol Infect. 2018;146(10):1308–11. https://doi.org/10.1017/S0950268818001346.
Autenrieth CS, Beck EJ, Stelzle D, Mallouris C, Mahy M, Ghys P. Global and regional trends of people living with HIV aged 50 and over: estimates and projections for 2000–2020. Lima VD, ed. PLoS ONE. 2018;13(11):e0207005. https://doi.org/10.1371/journal.pone.0207005.
Fitch KV, Anderson EJ, Hubbard JL, et al. Effects of a lifestyle modification program in HIV-infected patients with the metabolic syndrome. AIDS. 2006;20(14):1843–50. https://doi.org/10.1097/01.aids.0000244203.95758.db.
Juma K, Reid M, Roy M, Vorkoper S, Temu TM, Levitt NS, et al. From HIV prevention to non-communicable disease health promotion efforts in sub-Saharan Africa: a narrative review. AIDS. 2018;32:S63–73. https://doi.org/10.1097/QAD.0000000000001879.
Ordunez P, Martinez R, Niebylski ML, Campbell NR. Hypertension prevention and control in Latin America and the Caribbean. J Clin Hypertens. 2015;17(7):499–502. https://doi.org/10.1111/jch.12518.
Sanchez RA, Ayala M, Baglivo H, et al. Latin American guidelines on hypertension. J Hypertens. 2009;27(5):905–22. https://doi.org/10.1097/HJH.0b013e32832aa6d2.
Carroll A, Brew B. HIV-associated neurocognitive disorders: recent advances in pathogenesis, biomarkers, and treatment. F1000Res. 2017;6:312. https://doi.org/10.12688/f1000research.10651.1.
The Mind Exchange Working Group, Antinori A, Arendt G, et al. Assessment, diagnosis, and treatment of HIV-associated neurocognitive disorder: a consensus report of the mind exchange program. Clin Infect Dis. 2013;56(7):1004–17. https://doi.org/10.1093/cid/cis975.
Mahale P, Engels EA, Coghill AE, Kahn AR, Shiels MS. Cancer risk in older persons living with human immunodeficiency virus infection in the United States. Clin Infect Dis. 2018;67(1):50–7. https://doi.org/10.1093/cid/ciy012.
Medapalli RK, Parikh CR, Gordon K, Brown ST, Butt AA, Gibert CL, et al. Comorbid diabetes and the risk of progressive chronic kidney disease in HIV-infected adults: data from the veterans aging cohort study. J Acquir Immune Defic Syndr. 2012;60(4):393–9. https://doi.org/10.1097/QAI.0b013e31825b70d9.
White MC, Holman DM, Goodman RA, Richardson LC. Cancer risk among older adults: time for cancer prevention to go silver. Gerontologist. 2019;59(Supplement_1):S1–6. https://doi.org/10.1093/geront/gnz038.
Frank TD, Carter A, Jahagirdar D, Biehl MH, Douwes-Schultz D, Larson SL, et al. Global, regional, and national incidence, prevalence, and mortality of HIV, 1980–2017, and forecasts to 2030, for 195 countries and territories: a systematic analysis for the Global Burden of Diseases, Injuries, and Risk Factors Study 2017. Lancet HIV. 2019;6(12):e831–59. https://doi.org/10.1016/S2352-3018(19)30196-1.
Pacheco AG, Tuboi SH, Faulhaber JC, Harrison LH, Schechter M. Increase in non-AIDS related conditions as causes of death among HIV-infected individuals in the HAART era in Brazil. Novotny T, ed. PLoS ONE. 2008;3(1):e1531. https://doi.org/10.1371/journal.pone.0001531.
Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection; Chapter 5: Clinical guidelines: managing common coinfections and comorbidities. World Health Organization. https://www.who.int/hiv/pub/arv/chapter5.pdf?ua=1. Accessed July 15, 2020.
Acknowledgments
We would like to thank the library staff at Yale University School of Medicine and Universidad Peruana Cayetano Heredia. We would also like to thank the National Institute of Health Fogarty International Center for supporting this work.
Funding
Dr. Diego M. Cabrera serves as a Fogarty Global Health Trainee and is supported by the Fogarty International Center (FIC) at the National Institutes of Health (NIH) and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) under grant number D43TW010540. Dr. Monica M. Diaz serves as a Fogarty Global Health Trainee and is supported by the FIC at the NIH under grant number D43TW009343. Dr. Hsieh is supported by NIH/Fogarty International Center K01TW009995 and the Rheumatology Research Foundation K Supplement Award.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of Interest
The authors declare that they have no conflict of interest.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Disclaimer
The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
Additional information
The data in this manuscript has been presented as an abstract at the International Workshop on HIV & Aging 2020 (October 2, 2020; virtual conference).
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
DMC and MMD have contributed to this work equally and share first co-authorship.
This article is part of the Topical Collection on Global Health
Appendices
Appendix A: Search Strategy
Search for Ovid Embase
Additional databases provided upon request: Alyssa.grimshaw@yale.edu
1. exp Caribbean Islands/
2. exp Caribbean/
3. (Caribbean or Carib or West Indies).mp.
4. (Anguilla* or Antilles or Antigua* or Aruba* or Barbuda or Bahamas or Bahamian* or Barbados or Barbadian* or Barthelemy or Saint Barthelemois or Barts or Bermuda or Bermudian* or Bonaire or Bonairian* or Cuba* or Cayman or Caymanian* or Curacao* or Caicos or Belonger* or croix or Crucian* or Dominica or Dominican Republic or Dominican* or Santo Domingo).mp.
5. (Eustatius or Grenada or Grenadian* or Guadeloupe* or grenadines or Haiti* or Hispaniola or Jamaica* or Martinique or Martiniquais or Martinican* or Puerto Rico or Puerto Rican* or Nevis or Nevisian* or Montserrat* or Virgin Island or Virgin Islands or Virgin Islander or Virgin Islanders or Saba or Statia or Suriname* or Trinidad or Tobago or Trinidadian or Tobagonian or Tortola or Turks Island* or French Guiana or French Guianese or Leeward or Windward).mp.
6. (USVI or BVI).ti,ab.
7. ("St Lucia" or Saint Lucia or Lucian* or "St Kitts" or Saint Kitts or Kittian* or Saint Martin or "St Martin" or St Marteen or Saint Marteen or "St Thomas" or "St John" or Saint Thomas or Saint John or Sint Marteen or Water islander* or st thomian* or st johnian*).mp.
8. exp "South and Central America"/
9. (Costa Rica* or El Salvador or Salvadoran* or Guatemala* or Honduras or Honduran* or Nicaragua* or Nica or Nicoya or Pinolero or Nicaraguenses or Panama or Panamanian*).mp.
10. (Argentina* or Chile or Chilean* or Ecuador* or Paraguay* or Uruguay*).mp.
11. (Andean or Latin America* or Central America* or South America* or Bolivia* or Colombia* or Peru* or Venezuela* or Mexico or Mexican* or Brazil*).mp.
12. or/1-11
13. exp Human immunodeficiency virus infection/
14. (human immunodeficienc* or human immun* deficienc* or acquired immunodeficiency syndrome or HIV or AIDS or HIV?AIDS).tw,kw.
15. (Human T?Cell Lymphotropic Virus Type III or Human T?Cell Lymphotropic Virus Type III or LAV-HTLV-III or Lymphadenopathy Associated Virus or HTLV-III or HTLVIII?LAV).tw,kw.
16. 13 or 14 or 15
17. 12 and 16
18. exp kidney disease/
19. ((renal or kidney) and (disease or failure* or insufficienc* or injury or injuries or dysfunction*)).tw,kw.
20. (kidney tubular necrosis or lower nephron nephrosis or lower nephron nephroses).tw,kw.
21. exp Rhabdomyolysis/
22. exp Thrombotic Microangiopathies/
23. exp Glomerular Filtration Rate/
24. (nephropath* or Rhabdomyolysis or rhabdomyolses or Myoglobinuria* or Thrombotic Microangiopath* or urinary tract obstruction* or urinary obstruction* or urinary blockage* or tubulointerstitial renal or tubulo-interstitial renal or tubulointerstitial kidney* or tubulo-interstitial kidney* or Glomerular Filtration Rate*).tw,kw.
25. 18 or 19 or 20 or 21 or 22 or 23 or 24
26. 17 and 25
27. exp mood disorder/
28. exp cognitive defect/
29. exp neuropsychology/
30. exp "disorders of higher cerebral function"/
31. (Depression* or Depressive or Mood Disorder* or Mental Health or Affective Disorder* or neuropsychological or neuropsychiatric or dementia* or amentia* or senile* or senility or Alzheimer*).tw,kw.
32. ((Cognitive* or Neurocognitive*) adj3 (decline* or disorder* or impairment* or deterioration* or dysfunction*)).tw,kw.
33. 27 or 28 or 29 or 30 or 31 or 32
34. 17 and 33
35. exp malignant neoplasm/
36. (cancer* or malignanc* or neoplasm* or neoplasia* or tumor* or tumour* or leukemia* or carcinoma* or melanoma* or lymphoma).tw,kw.
37. (Human papillomavirus or human papilloma virus or HPV).tw,kw.
38. 35 or 36 or 37
39. 17 and 38
40. exp spine fracture/
41. exp hip fracture/
42. exp Bone Diseases, Metabolic/
43. exp bone mass/ or exp bone density/
44. (bone mass or bone densit* or bone mineral densit* or vertebral fracture* or spinal fracture* or hangman* fracture* or Intertrochanteric fracture* or hip fracture* or Trochanteric fracture* or Subtrochanteric fracture* or Vitamin D or Calcium or Body composition measurement* or frailty or osteopenia* or low bone densit* or bone disease* or osteoporosis or osteoporoses or bone loss).tw,kw.
45. 40 or 41 or 42 or 43 or 44
46. 17 and 45
47. exp cardiovascular disease/
48. exp Cholesterol/
49. (cardiovascular disease* or heart disease* or heart failure or stroke* or cerebrovascular accident* or Apoplex* or brain vascular accident* or heart attack* or myocardial infarct* or blood pressure* or hyperlipidemia* or Lipidemia* or Lipemia* or Hyperlipemia* or high blood pressure* or hypertension or Epicholesterol or cholesterol or cardiac fat infiltration* or myocardial fibrosis or cardiac fibrosis or left ventricular or systolic dysfunction* or diastolic dysfunction* or Atrial Fibrillation* or Thromboembolism* or Arteriosclerosis or Arterioscleroses or Coronary Artery Disease*).tw,kw.
50. 47 or 48 or 49
51. 17 and 50
52. (non-aids event* or non aids event* or serious clinical event* or non-aids clinical event* or non aids clinical event* or non-aids-related event* or non aids related event* or non-aids defining cancer* or non aids defining cancer* or NACD or NACDs or non-aids defining event* or non aids defining event* or non-aids morbidit* or non-aids morbidi* or non-aids endpoint* or non aids endpoint* or non-aids comorbidit* or non aids comorbidit*).tw,kw.
53. 12 and 52
54. 26 or 34 or 39 or 46 or 51 or 53
Appendix B: Table of Excluded Studies
Rights and permissions
About this article
Cite this article
Cabrera, D.M., Diaz, M.M., Grimshaw, A. et al. Aging with HIV in Latin America and the Caribbean: a Systematic Review. Curr HIV/AIDS Rep 18, 1–47 (2021). https://doi.org/10.1007/s11904-020-00538-7
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11904-020-00538-7