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Southern African Journal of HIV Medicine logoLink to Southern African Journal of HIV Medicine
. 2020 Dec 10;21(1):1164. doi: 10.4102/sajhivmed.v21i1.1164

Profile of elderly patients receiving antiretroviral therapy at Newlands Clinic in 2020: A cross-sectional study

Cleophas Chimbetete 1,✉, Tinashe Mudzviti 1,2, Tinei Shamu 1,3
PMCID: PMC7736656  PMID: 33354366

Abstract

Background

People living with HIV (PLWH) face new challenges such as accelerated ageing and higher rates of comorbidities including cardiovascular, renal and metabolic diseases as they age.

Objectives

To profile the demographic and clinical characteristics of elderly patients receiving HIV care at Newlands Clinic (NC), Harare, Zimbabwe, as of 01 October 2019.

Methods

A cross-sectional analysis was conducted using clinic data. All patients who were 50 years and older on 01 October 2019 were enrolled. Descriptive statistics (medians, interquartile ranges [IQRs] and proportions) were used to describe patient demographic and clinical characteristics.

Results

Out of 6543 patients undergoing care at NC, 1688 (25.8%) were older than 50 years. The median duration of antiretroviral therapy (ART) was 10.9 years (IQR: 7.1–13). Over 90% of all patients had an HIV viral load below 50 copies/mL. Women were more likely than men to be overweight and obese (32% and 25% vs. 18% and 7%, respectively). Hypertension (41.2%), arthritis (19.9%) and chronic kidney disease (11.6%) were common comorbidities differently distributed based on sex. The most common malignancy diagnosed in women was cervical intra-epithelial neoplasia (68% of cancer burden in women) and Kaposi sarcoma was the leading malignancy in men (41% of cancer burden in men). Nearly 20% of patients had at least two chronic non-communicable comorbidities and 5.6% had at least three.

Conclusion

A high burden of comorbidities was observed amongst HIV-positive elderly patients receiving ART. Age-appropriate monitoring protocols must be developed to ensure optimum quality of care for elderly HIV-positive individuals.

Keywords: HIV infection, elderly patients, comorbidities, ART, Zimbabwe

Introduction

Effective antiretroviral therapy (ART) has changed the course of human immunodeficiency virus (HIV) infection from being considered a fatal illness to a chronic manageable condition. This has enabled people to grow old living with HIV. The number of people who are more than 50 years old and living with HIV has increased globally because of the success of national ART programmes and the control of new infections amongst the elderly.1 The life expectancy of people living with HIV (PLWH) has increased substantially, approximating that of the general population in high-income countries.2,3 Similar gains in life expectancy have also been reported in some countries in sub-Saharan Africa.4 It seems likely that the median age of PLWH will increase with time as more and more people garner the survival benefits of effective ART. It is now critical to promote healthy ageing amongst PLWH, an achievement that some have described as the ‘fourth 90%’.5

As PLWH age, they face many of the same health challenges as faced by older individuals in the general population. Additionally, ageing PLWH face new challenges such as accelerated ageing and higher rates of comorbidities including cardiovascular, renal and metabolic diseases.6 Comorbidities occur at high rates at all ages amongst PLWH but become increasingly important as this population ages. People living with HIV also develop geriatric syndromes and frailty earlier as compared to HIV uninfected people.7 Certain ART drugs such as protease inhibitors may increase cardiovascular risk because of poor metabolic profile including hyperlipidaemia compared to other drugs such as the non-nucleoside reverse transcriptase inhibitors.8 There has been a documented increase in the rate of all cancers, particularly lung, prostate, colorectal, anal, cervix, lymphomas and breast as PLWH age.9 However, it is important to note that cancer rates increase with age in everyone.

Although there is a growing body of research on HIV and ageing, evidence from low- and middle-income countries that bear the highest burden of HIV infection is scarce.10,11 The expectations and management of elderly PLWH differ from those of younger patients and may change over time. In this study, we profiled the demographic and clinical characteristics of elderly patients receiving comprehensive HIV care at Newlands Clinic (NC), Harare, Zimbabwe, as of 01 October 2019. There is evidence that the distribution of comorbidities may differ by sex12; therefore, we analysed and reported our results by sex.

Methods

Study design

This study utilised a cross-sectional analysis of routinely collected electronic clinic data.

Study setting

The study was conducted at Newlands Clinic, Harare, Zimbabwe. Newlands Clinic, operated by the Ruedi Luethy Foundation, is a model public–private partnership with the Ministry of Health and Child Care. Since 2004 the clinic has offered comprehensive HIV treatment and care to individuals living with HIV. Operations of the clinic have been previously described.13 The clinic’s electronic database captures patient-level data on laboratory test results, diagnoses, medications and demographic variables.

Sampling

Patients ≥ 50 years were defined as elderly. All patients who were 50 years and older as on 01 October 2019 were included in the analysis. The study had no exclusion criteria for enrolment.

Data analysis

Routinely collected electronic patient data were abstracted from the clinic’s electronic database using custom structured language queries and exported to Excel. Records were de-identified at abstraction and assigned numeric unique identifiers. Stata version 13 was used for analysis. The most recent CD4 cell count and HIV viral load (VL) were defined as the last test result documented in the patient’s clinic notes taken within the preceding year. Weight categories were defined using body mass index (BMI) as follows: underweight (BMI < 18 kilogram/square meter [kg/m2]), normal weight (BMI of 18 kg/m2 – 25 kg/m2), overweight (BMI > 25 kg/m2 – 30 kg/m2) and obese (BMI > 30 kg/m2). Baseline age was defined as age at the date of initiating ART. Descriptive statistics (medians, interquartile ranges [IQRs] and proportions) were used to describe patient demographic and clinical characteristics. Diagnosis of comorbidities was conducted based on the following existing national guidelines: diabetes mellitus (DM) is defined as either fasting blood sugar ≥ 7.0 millimoles per litre (mmol/L) or random blood sugar of ≥ 11 mmol/L, if it still remains high after 3 months, then treatment is instituted. Hypertension is defined as two blood pressure readings > 140/90 millimetre of mercury (mmHg) at least 6 h apart. Chronic kidney disease (CKD) is defined as a serum creatinine clearance of < 60 milligrams per deciliter (mg/dL) confirmed with a second result within 3–6 months. All cancers ever diagnosed were included in the analysis and the pre-cancer conditions of vulva and cervical intra-epithelial neoplasia (VIN and CIN) were included as well.

Weight and height measurements were performed by nurses in the consulting rooms using Seca 752 or Seca 952 scales and wall-mounted height measure tapes, respectively. Before being weighed, patients removed shoes, jackets and emptied their pockets. Samples for blood glucose measurement were collected into 4-mL BD Vacutainer Plus plastic tubes with 10 mg sodium fluoride and 8 mg potassium oxalate additives. Blood samples for creatinine measurement were collected into 4-mL BD Vacutainer Plus plastic serum tubes with clot activator and silicone-coated interior. Glucose and creatinine measurements were conducted at the on-site laboratory on a COBAS Integra 400 plus instrument using the hexokinase and Jaffe reaction methods, respectively.

Ethical consideration

Permission to carry out the study was granted by the Newlands Clinic local research board. Ethical approval was granted by the Medical Research Council of Zimbabwe, approval number: A1336. Participants consented to publication as part of the informed consent process.

Results

Of the 6543 patients in care at NC, 1688 (25.8%) were above the age of 50 years (Table 1). The median age at analysis was 56 years (IQR: 52–61), with 72.2% of elderly patients aged between 50 and 60 years, and no difference by sex. The median duration of ART was 10.9 years (IQR: 7.1–13). At enrolment into care, 51% were married, 32% widowed, 6% divorced and 11% single. There was a far lower proportion of married women than married men (31% vs. 82%). The most recent median CD4 cell count in this cohort was 464 cells/mm3 (IQR: 327–628), which was higher in females than males (526 vs. 377). Over 90% of all patients were virally suppressed, with VLs below 50 copies/mL. Only 1.8% of patients had a VL > 1000 copies/mL. No sex differences were observed in the VL distribution. Almost half of the elderly patients were either overweight or obese and 8% were underweight. Women were more likely than men to be overweight and obese (32% and 25% vs. 18% and 7%, respectively). Most patients (64.1%) received the fixed dose ART combination of tenofovir, lamivudine and dolutegravir.

TABLE 1.

Demographic and clinical characteristics of elderly patients receiving antiretroviral therapy at Newlands Clinic in March 2020, by sex.

Characteristic Females
Males
Total
n = 1008 % n = 680 % N = 1688 %
Baseline age in years, median (IQR) 46.5 41.2–51.4 46.8 42.7–52.1 46.6 42.1–51.8
Current age (years), median (IQR) 56 52–61 56 52–61 56 52–61
Current age in years, n (%)
50–60 729 72 491 72 1220 72
> 60–70 246 25 158 23 404 24
> 70 33 3 31 5 64 4
Marital status at enrolment
Married 308 31 556 82 864 51
Widowed 478 47 69 10 547 32
Divorced 74 7 27 4 101 6
Single 148 15 28 4 176 11
CD4 count in cells/µL, median (IQR) 526 390–689 377 390–689 464 327–628
HIV viral load expressed as RNA copies/mL, n (%)
< 50 939 93 617 91 1 756 92
50–1000 58 6 39 6 97 6
> 1000 9 1 21 3 30 2
Body mass index category, n (%)
Underweight 48 5 88 13 136 8
Normal 380 38 406 60 786 47
Overweight 319 32 133 18 452 27
Obese 251 25 48 7 299 18
ART duration, years, median (IQR) 11.3 8.1–14.1 10.4 8.1–14.1 10.9 7.1–13
Current ART regimen, n (%)
NNRTI† +2NRTI 144 14 97 14 241 14
TLD‡ 671 67 411 60 1 082 64
ATV/r§ or LPV/r + 2NRTI 171 17 143 21 314 19
DTG†† + Darunavir + ≤ 2NRTI 17 2 28 4 45 3
Other regimens 5 0.5 1 0.2 6 0.3

ART, antiretroviral therapy; IQR, interquartile range; HIV, human immunodeficiency virus; RNA, ribonucleic acid; NNRTI, non-nucleoside reverse transcriptase inhibitors; NRTI, nucleoside reverse transcriptase inhibitor; TLD, tenofovir, lamivudine and dolutegravir; ATV/r, atazanavir/ritonovir; LPV/r, Lopinavir/ritonovir; DTG, dolutegravir.

†

, Either nevirapine or efavirenz.

‡

, Tenofovir, lamivudine and dolutegravir.

§

, Atazanavir/ritonavir.

, Lopinavir/ritonavir.

††

, Dolutegravir.

Comorbidities and pill burden

Hypertension, arthritis and any malignancy were common comorbidities differently distributed by sex (Table 2). Hypertension was the most common comorbidity, with 704 (41.2%) patients having a documented diagnosis of hypertension. A higher proportion of women as compared to men had hypertension (48.5% vs. 31.6%, respectively). Arthritis was the second most common comorbidity and higher amongst women compared to men (24.5% vs. 13.1%), as was any malignancy (11.2% compared with 2.5%). Other comorbidities included DM (7.2%), CKD (11.6%) and congestive cardiac failure (2.2%), which were similarly distributed in men and women. Nearly 20% of patients had at least two chronic non-communicable comorbidities and 5.6% had three (Figure 1). Almost half of the cohort (47%) received an additional chronic medicine other than ART.

TABLE 2.

Distribution of comorbidities amongst elderly patients receiving antiretroviral therapy at Newlands Clinic in March 2020, by sex.

Comorbidity Females
Males
Total
n = 1008 60% n = 680 40% n = 1680 100%
Hypertension 489 48.5 215 31.6 704 41.2
Diabetes mellitus 68 6.8 53 7.8 117 7.2
Chronic kidney disease† 108 10.7 87 12.8 195 11.6
Any malignancy 113 11.2 17 2.5 130 7.7
Congestive cardiac failure 27 2.7 10 1.5 37 2.2
Arthritis 247 24.5 89 13.1 336 19.9
Tuberculosis 187 19 176 26 363 22
†

, Chronic kidney disease = glomerular filtration rates of <60 mL/min/1.73 m2.

FIGURE 1.

FIGURE 1

Distribution of comorbidities and additional chronic medicines amongst elderly patients receiving antiretroviral therapy at Newlands Clinic in March 2020.

Burden of malignancies ever diagnosed

Amongst women, the most common malignancy diagnosed was CIN3, accounting for 68% of the malignancy burden (Table 3). Other common malignancies in women included cancer of the cervix (12%) and VIN (9%). Amongst men, the most common malignancy was Kaposi Sarcoma (41%), followed by lymphomas and penile cancer (24%).

TABLE 3.

Distribution of malignancies amongst elderly patients receiving antiretroviral therapy at Newlands Clinic in March 2020, by sex.

Malignancy type Female
Male
Frequency
n = 113 % n = 17 % n = 130 %
CIN 3 77 68 - - 77 59
Cancer of the cervix 14 12 - - 14 11
Kaposi sarcoma 4 4 7 41 11 9
VIN 3 10 9 - - 10 8
Lymphomas† 3 3 4 24 7 5
Penile cancer - 4 24 4 3
Vulvar cancer 3 3 - - 3 2
Multiple myeloma 1 1 1 6 2 2
Anal cancer 1 1 0 - 1 1
Cancer of eye 1 1 0 - 1 1
Cancer of rectum 1 1 0 - 1 1

CIN, cervical intra-epithelial neoplasia; VIN, vulvar intra-epithelial neoplasia.

†

, Lymphomas, four non-Hodgkin’s, one central nervous system, one Hodgkin’s, and one immunoblastic.

Discussion

We found that a quarter of PLWH receiving care at NC were older than 50 years. The majority of these elderly patients had received ART for over 10 years. Most men were married; the majority of women were widowed. This cohort of elderly patients had well-controlled HIV infection with evidence of good immunological status. A high prevalence of overweight or obesity was reported, particularly amongst women. Comorbidities were common, notably hypertension, malignancies (far higher in women than in men) and CKD (higher in men than in women). Nearly 20% of patients had at least two chronic comorbidities, and 5.6% had three.

The goal of ART is sustained suppression of HIV replication. Our results show that elderly patients with HIV achieve high rates of viral suppression. This finding is consistent with the results from other studies.10 Older patients receiving ART have demonstrated good medication adherence and this plays a key role in achieving high rates of viral suppression.14,15

Although only half of our patients were married at the time of enrolment into care, over 80% of men were married. The higher proportion of marriage amongst men may be because of the fact that men are more likely to remarry after the loss of a spouse or after divorce.16 Older patients with HIV face a number of challenges that may affect their quality of life. Loss of partners and friends may lead to social isolation, depression and poor adherence to medicines.17 Additional stressors such as unemployment and poverty may further worsen the quality of life. The high number of comorbidities and pill burden may negatively affect medicine adherence. Interactions between ART and other medications are a major consideration amongst the ageing population.

The high prevalence of chronic non-AIDS diseases in this cohort is consistent with the findings from other studies which have showed an increased number of comorbidities in PLWH at all ages, but particularly as this population ages.6 Hypertension is now recognised as an important chronic comorbid condition of PLWH and is associated with increased morbidity and mortality.18 Screening and optimal management of hypertension must become part of the comprehensive care of elderly PLWH.

The prevalence of CKD was high. Numerous risk factors are involved in renal disease in PLWH, such as age, black race, DM, hypertension, low CD4 counts and certain ART medicines like tenofovir disoproxil fumarate.19 All HIV-positive patients especially the elderly must have annual measurements of their renal function. Diabetes mellitus was far less common than hypertension. As has been previously reported, the risk of developing DM in PLWH is not well-established, and studies have not consistently shown a relationship between DM and HIV.20,21 However, some studies have shown that the risk of DM increases amongst patients receiving ART.22

A large number of elderly patients suffered from different forms of malignancies, which were differently distributed by sex. Human papilloma virus (HPV)-related malignancies were the leading diagnosed cancers. Almost 70% of the women with malignancies had HPV-related CIN3. The HPV-related anogenital malignancies will remain a challenge amongst HIV-infected men and women even in the era of effective ART.23 Screening for high-risk HPV infection should become part of the care of HIV-positive women. The estimated cumulative incidence for other cancers such as non-Hodgkin’s B-cell lymphoma, lung cancer, liver cancer and Hodgkin’s lymphoma increased amongst HIV-infected patients.24 Routine screening for common cancers should be part of the comprehensive care of HIV-infected elderly patients.

Our study was strengthened by very high levels of data completeness. However, our study was limited as we used data from a single clinic only. Frailty, cognitive impairment and other geriatric syndromes that are common and important in HIV were not included in comorbidities as data on these are not routinely collected. Furthermore, assessing cancers cross sectionally as we did, without consideration of those who have died of cancer prior to the data pull, underestimates the true cancer burden. We assessed all cancers ever diagnosed (historical). We acknowledge that although these data are interesting, they are potentially misleading. Despite these limitations, we believe that our results are important to healthcare providers and policymakers.

Conclusion

Our data demonstrates that in Africa high rates of virological suppression can be achieved amongst elderly patients on ART. However, the high rates of obesity (especially amongst women) and hypertension in this population need to be addressed. The prevalence of pre-malignant cervical disease amongst elderly women is high; and hence, routine cervical cancer screening is essential for elderly women living with HIV.

The time has come for HIV treatment programmes to draw on a wide range of medical disciplines and evidence-based screening procedures for the multidisciplinary care of the ageing HIV-infected population. Age-appropriate monitoring protocols must be developed to ensure optimum quality of care for elderly HIV-positive individuals.

Acknowledgements

The authors would like to acknowledge Newlands Clinic staff and patients. Furthermore, we acknowledge Morna Cornell who mentored us during the writing process.

Competing interests

The authors have no competing interests to declare.

Authors’ contributions

All authors were involved in designing the study. T.S. and C.C. conducted the data analysis. C.C. prepared the draft manuscript. T.S. and T.M. reviewed the draft manuscript. C.C. prepared the final manuscript for publication.

Funding information

Study did not receive any funding. Analysis is conducted as part of the routine clinic work.

Data availability statement

The data sets used and/or analysed during the current study are available from the corresponding author upon request.

Disclaimer

The views expressed in this article are those of the authors’ and do not necessarily reflect the official policy or position of any affiliated agency of the authors.

Footnotes

How to cite this article: Chimbetete C, Mudzviti T, Shamu T. Profile of elderly patients receiving antiretroviral therapy at Newlands Clinic in 2020: A cross-sectional study. S Afr J HIV Med. 2020;21(1), a1164. https://doi.org/10.4102/sajhivmed.v21i1.1164

References

  • 1.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. PLoS One. 2018;13(11):e0207005 10.1371/journal.pone.0207005 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Wandeler G, Johnson LF, Egger M. Trends in life expectancy of HIV-positive adults on antiretroviral therapy across the globe: Comparisons with general population. Curr Opin HIV AIDS. 2016;11(5):492–500. 10.1097/COH.0000000000000298 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Teeraananchai S, Kerr SJ, Amin J, Ruxrungtham K, Law MG. Life expectancy of HIV-positive people after starting combination antiretroviral therapy: A meta-analysis. HIV Med. 2017;18(4):256–266. 10.1111/hiv.12421 [DOI] [PubMed] [Google Scholar]
  • 4.Asiki G, Reniers G, Newton R, et al. Adult life expectancy trends in the era of antiretroviral treatment in rural Uganda (1991–2012). AIDS. 2016;30(3):487–493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Harris TG, Rabkin M, El-Sadr WM. Achieving the fourth 90: Healthy aging for people living with HIV. AIDS. 2018;32(12):1563–1569. 10.1097/QAD.0000000000001870 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Smit M, Brinkman K, Geerlings S, et al. Future challenges for clinical care of an ageing population infected with HIV: A modelling study. Lancet Infect Dis. 2015;15(7):810–818. 10.1016/S1473-3099(15)00056-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Greene M, Covinsky KE, Valcour V, et al. Geriatric syndromes in older HIV-infected adults. J AIDS. 2015;69(2):161–167. 10.1097/QAI.0000000000000556 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Wing EJ. HIV and aging. Int J Infect Dis. 2016;53(1):61–68. 10.1016/j.ijid.2016.11.414 [DOI] [PubMed] [Google Scholar]
  • 9.Jilich D, Sedl S, Nielsen LN, et al. Infection-related and -unrelated malignancies, HIV and the aging population. HIV Med. 2016;17(8):590–600. [DOI] [PubMed] [Google Scholar]
  • 10.Agaba PA, Meloni ST, Sule HM, et al. Treatment outcomes among older human immunodeficiency virus-infected adults in Nigeria. Open Forum Infect Dis. 2017;4(2):ofx031 10.1093/ofid/ofx031 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Cornell M, Johnson LF, Schomaker M, et al. Age in antiretroviral therapy programmes in South Africa: A retrospective, multicentre, observational cohort study. Lancet HIV. 2015;2(9):368–375. 10.1016/S2352-3018(15)00113-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Brañas F, Sánchez-Conde M, Carli F, et al. Sex differences in people aging with HIV. J Acquir Immune Defic Syndr. 2020;83(3):284–291. 10.1097/QAI.0000000000002259 [DOI] [PubMed] [Google Scholar]
  • 13.Shamu T, Chimbetete C, Shawarira-Bote S, Mudzviti T, Luthy R. Outcomes of an HIV cohort after a decade of comprehensive care at Newlands Clinic in Harare, Zimbabwe: TENART cohort. PLoS One. 2017;12(10):e0186726 10.1371/journal.pone.0186726 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Ghidei L, Simone M, Salow M, et al. Aging, antiretrovirals, and adherence: A meta analysis of adherence among older HIV-infected individuals. Drugs Aging. 2013;30(10):809–819. 10.1007/s40266-013-0107-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Soomro N, Fitzgerald G, Seeley J, Schatz E, Nachega JB, Negin J. Comparison of antiretroviral therapy adherence among HIV-infected older adults with younger adults in Africa: Systematic review and meta-analysis. AIDS Behav. 2019;23(2):445–458. 10.1007/s10461-018-2196-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Carr D. Marital transitions: Widowhood, divorce, and remarriage In: Whitbourne SK, editors. The encyclopedia of adulthood and aging. Hoboken, NJ: John Wiley & Sons, 2015; p. 1–5. [Google Scholar]
  • 17.Heestermans T, Browne JL, Aitken SC, Vervoort SC, Klipstein-Grobusch K. Determinants of adherence to antiretroviral therapy among HIV-positive adults in sub-Saharan Africa: A systematic review. BMJ Glob Health. 2016;1(4):1–13. 10.1136/bmjgh-2016-000125 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Nguyen KA, Peer N, Mills EJ, Kengne AP. Burden, determinants, and pharmacological management of hypertension in HIV-positive patients and populations: A systematic narrative review. AIDS Rev. 2015;17(2):83–95. [PubMed] [Google Scholar]
  • 19.Abraham AG, Crane AH, Eron J, et al. End-stage renal disease among HIV-infected adults in North America. Clin Infect Dis. 2015;60(6):941–949. 10.1093/cid/ciu919 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Rasmussen LD, Mathiesen ER, Kronborg G, Gerstoft J, Obel N. Risk of diabetes mellitus in persons with and without HIV: A Danish nationwide population-based cohort study. PLoS One. 2012;7(9):e44575 10.1371/journal.pone.0044575 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Monroe AK, Glesby MJ, Brown TT. Diagnosing and managing diabetes in HIV-infected patients: Current concepts. Clin Infect Dis. 2015;60(3):453–462. 10.1093/cid/ciu779 [DOI] [PubMed] [Google Scholar]
  • 22.Lin SP, Wu CY, Wang CB, Li TC, Ko NY, Shi ZY. Risk of diabetes mellitus in HIV-infected patients receiving highly active antiretroviral therapy: A nationwide population-based study. Medicine (Baltimore). 2018;97(36):e12268 10.1097/MD.0000000000012268 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Palefsky JM. HPV-associated anal and cervical cancers in HIV-infected individuals: Incidence and prevention in the antiretroviral therapy era. Curr Opin HIV AIDS. 2017;12(1):26–30. 10.1097/COH.0000000000000336 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Silverberg MJ, Lau B, Achenbach CJ, et al. Cumulative incidence of cancer among persons with HIV in North America: A cohort study. Ann Intern Med. 2015;163(7):507–518. 10.7326/M14-2768 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data sets used and/or analysed during the current study are available from the corresponding author upon request.


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