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editorial
. 2026 Jun 10;139(19):2845–2847. doi: 10.1097/CM9.0000000000004127

Focusing on vulnerable populations in HIV

Hang Qi 1,2, Taisheng Li 1,3,4,✉
Editor: Yanjie Yin
PMCID: PMC13626690  PMID: 42268263

The global human immunodeficiency virus (HIV) epidemic remains a major public health challenge, with an estimated 40.8 million people living with HIV (PLWH) worldwide by the end of 2024. Despite expanding combination antiretroviral therapy (cART) coverage to 31.6 million in 2024, HIV-related illnesses still caused approximately 630,000 global deaths.[1]

cART has successfully suppressed HIV replication and transmission, significantly extending the life expectancy of PLWH. However, the mortality burden has shifted toward non-acquired immunodeficiency syndrome (AIDS)-defining diseases (NADs), including metabolic syndrome, cardiovascular and cerebrovascular diseases, non-AIDS-defining cancers (NACs), and organ dysfunctions (liver, renal, and bone).[2] Achieving sustained survival requires a more comprehensive approach to HIV management.

Improving the prognosis of PLWH depends on clinicians’ ability to identify those in need of specialized care. To better identify PLWH at elevated risk of poor outcomes and guide targeted interventions, we propose the concept of “vulnerable populations in HIV”, encompassing those who require intensified monitoring and individualized management.

Definition

The concept of “vulnerable populations in HIV” encompasses PLWH at heightened risk of adverse outcomes despite effective cART. This category includes: (1) Advanced age ( ≥50 years old); (2) Incomplete immune reconstitution despite virologic suppression; (3) Presence of at least one comorbidity (NAD, e.g., metabolic syndrome, cardiovascular or cerebrovascular disease, chronic liver, renal, or bone disorder, or NACs); (4) Coexisting mental disorders (e.g., depression, anxiety, insomnia, and substance abuse); (5) Polypharmacy (≥2 long-term medications in addition to cART); (6) Intravenous drug use; (7) Special populations (e.g., children, pregnant and postpartum women).

Reasons for Proposing “Vulnerable Populations in HIV”

Advanced age

The number of older PLWH, defined as those ≥50 years of age,[3] is growing worldwide.[4] Older PLWH constitute a uniquely vulnerable demographic due to converging biological and psychosocial risks. First, older PLWH experience higher burdens of chronic multimorbidity than the general population, increasing treatment complexity, adverse events, and the likelihood of polypharmacy.[5] They also show evidence of earlier onset of age-related comorbidities; for example, study reports that more than half of PLWH aged ≥50 years have a heart age at least ten years older than their chronological age.[6] Second, evidence showed that they experience accelerated biological aging and immunosenescence even under effective cART.[7] Third, older PLWH face compounded challenges, including insufficient HIV knowledge and risk awareness, poor health literacy, limited patient–provider communication,[8] and the “double stigma” of HIV and ageism.[9]

Incomplete immune reconstitution

Although the introduction of cART has reduced AIDS-related mortality among PLWH, a subset of patients fails to achieve adequate CD4+ T-cell recovery despite sustained viral suppression, a condition termed immunological nonresponse (INR). Across studies, INRs have been defined inconsistently, either as failure to reach a specified CD4+ T-cell threshold (e.g., >200, >250, >350, >400, or >500 cells/µL) or as failure to achieve a minimum percentage increase from baseline (e.g., <5%, <20%, or <30%) over varying follow-up periods. The burden of INR remains substantial, with prevalence estimates ranging from 10% to 40% of treated individuals.[10] Given this heterogeneity, we adopt a common threshold CD4+ T-cell ≤500 cells/µL after several years of cART who maintain viral suppression according to the Department of Health and Human Services.[11] This cutoff is well supported by evidence showing that CD4+ T-cell ≥500 cells/µL approximates immunologic normalization according to the World Health Organization,[12] and patients who achieve it have morbidity and mortality comparable to HIV-negative individuals.[13] Large-scale cohort studies indicate that INRs face an increased risk of mortality compared to immune responders.[14] Additionally, this population exhibits heightened vulnerability to NADs, such as cardiovascular disease[15] and NACs.[16] Therefore, INR patients constitute a vulnerable group requiring a comprehensive management strategy that combines extending prophylaxis for opportunistic infections, optimizing vaccinations, and rigorously screening for coinfections. Crucially, clinicians must prioritize preventing NADs through aggressive cardiovascular risk management, routine cancer screening, and lifestyle interventions.[11]

Comorbidities

With increasing life expectancy and prolonged cART, PLWH face an elevated burden of NADs compared to uninfected controls, affecting approximately 38% of PLWH.[17] Specifically, meta-analyses indicate a 2.16-fold increased risk of cardiovascular events[18] and a 1.5-fold higher incidence of NACs despite viral suppression.[19] Metabolic syndrome affects approximately 21.5% of PLWH, 2-fold higher than in uninfected populations.[20]

PLWH with comorbidities constitute a distinctively vulnerable subgroup because studies confirm that multimorbidity is now the strongest predictor of mortality in virally suppressed PLWH.[2] This burden contributes adverse outcomes, including frailty, functional decline, and disability, which drive recurrent hospitalizations and reduced quality of life. Furthermore, the complexity of managing these conditions exacerbates the risk of polypharmacy, introducing safety concerns.[21]

To mitigate these risks, management must shift toward an integrated, multidisciplinary model. Clinicians should prioritize medication reconciliation to minimize drug–drug interactions (DDIs) and adopt aggressive preventive strategies. Comprehensive care must integrate routine screening for malignancies and lifestyle interventions to preserve long-term quality of life.

Mental disorders

Mental disorders (e.g., depression, anxiety, insomnia, and substance abuse) affecting 28–62% of the PLWH,[22] substantially higher than in the general population, significantly influence both the life expectancy and quality of life of PLWH. Furthermore, studies indicate that insomnia symptoms affect more than half of PLWH.[23] Mental disorders affect HIV testing uptake, cART initiation and adherence, retention in care, and are associated with increased mortality.[24] Therefore, early identification and management of mental disorders in PLWH constitute a critical component of comprehensive HIV care.

Polypharmacy

PLWH are at increased risk of polypharmacy and potential DDIs, largely driven by the growing burden of comorbidities.[21] DDIs can compromise treatment by increasing drug toxicity, reducing cART efficacy, and promoting the development of drug resistance. In clinical practice, these risks can be mitigated by selecting regimens with minimal interaction potential and by appropriate dose adjustment and monitoring. Comprehensive management of PLWH should emphasize the prevention, detection, and management of concomitant medication issues to preserve cART effectiveness, minimize adverse drug reactions, prevent DDIs, improve adherence, and reduce healthcare costs.

Intravenous drug use

Studies indicate that individuals who inject drugs exhibit poorer medication adherence, which increases the risk of viral resistance and limits subsequent treatment options.[25] In managing this population, clinicians should not only optimize antiretroviral regimens but also provide support for substance use cessation, enhance education on drug-related risks, and facilitate access to appropriate social and rehabilitation services.

Special physiological populations

Children face developmental challenges, dependence on caregivers for seeking care, and lifelong treatment burdens. Pregnant and postpartum women undergo physiological changes that alter pharmacokinetics and carry the critical risk of vertical transmission. Both require specialized medication counseling and monitoring to mitigate vulnerabilities.

Conclusion

The concept of vulnerable populations in HIV underscores the need to move beyond virologic suppression as the sole marker of treatment success and to address the broader spectrum of health risks faced by PLWH. By systematically identifying and prioritizing high-risk individuals, this framework can inform clinical decision-making, optimize resource allocation, and support more comprehensive, patient-centered care. Ultimately, addressing the needs of these vulnerable groups is integral to improving long-term outcomes and advancing the global HIV response.

Funding

This study was supported by the Special Research Fund for the Central High-level Hospitals of Peking Union Medical College Hospital (No. 2022-PUMCH-D-008), Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Sciences (No. 2021-I2M-1-037), and National Key Technologies R&D Program for the 13th Five-year Plan (No. 2017ZX10202101-001).

Conflics of interest

None.

Footnotes

How to cite this article: Qi H, Li TS. Focusing on vulnerable populations in HIV. Chin Med J 2026;139:2845–2847. doi: 10.1097/CM9.0000000000004127

References

  • 1.World Health Organization . HIV statistics, globally and by WHO region. World Health Organization, 2025. [Last accessed on Oct 16, 2025]. [Google Scholar]
  • 2.Smith CJ Ryom L Weber R Morlat P Pradier C Reiss P, et al. Trends in underlying causes of death in people with HIV from 1999 to 2011 (D:A:D): A multicohort collaboration. Lancet 2014;384:241-248. doi: 10.1016/S0140-6736(14)60604-8. [DOI] [PubMed] [Google Scholar]
  • 3.Ambrosioni J Levi LI Alagaratnam J Sempere A Mastrangelo A Paioni P, et al. Major revision version 13.0 of the European AIDS Clinical Society guidelines 2025. HIV Med 2026;27:18-32. doi: 10.1111/hiv.70120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.O’Connor SM Song R Viguerie A Buchacz K Lyles CM Farnham PG, et al. Projected increases in older people with HIV in the United States through 2040. Open Forum Infect Dis 2025;12:ofaf656. doi: 10.1093/ofid/ofaf656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Orlando G Zona S Menozzi M Carli F Garlassi E Berti A, et al. Premature age-related comorbidities among HIV-infected persons compared with the general population. Clin Infect Dis 2011;53:1120-1126. doi: 10.1093/cid/cir627. [DOI] [PubMed] [Google Scholar]
  • 6.Palella FJ Hart R Armon C Tedaldi E Yangco B Novak R, et al. Non-AIDS comorbidity burden differs by sex, race, and insurance type in aging adults in HIV care. AIDS 2019;33:2327-2335. doi: 10.1097/QAD.0000000000002349. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Montano M, Oursler KK, Xu K, Sun YV, Marconi VC. Biological ageing with HIV infection: Evaluating the geroscience hypothesis. Lancet Healthy Longev 2022;3:e194-e205. doi: 10.1016/s2666-7568(21)00278-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Marano-Lee M, Williams W, Xu S, Williams N, Moore A, Uhl G. Adults aged ≥50 years reached by the CDC’s HIV programs including HIV testing, PrEP referrals, and linkage to care in the United States, Puerto Rico, and the US Virgin Islands, 2019–2022. J Acquir Immune Defic Syndr 2025;100:209-216. doi: 10.1097/QAI.0000000000003723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Brown MJ, Adeagbo O. HIV and aging: Double stigma. Curr Epidemiol Rep 2021;8:72-78. doi: 10.1007/s40471-021-00265-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Yang X, Su B, Zhang X, Liu Y, Wu H, Zhang T. Incomplete immune reconstitution in HIV/AIDS patients on antiretroviral therapy: Challenges of immunological non-responders. J Leukoc Biol 2020;107:597-612. doi: 10.1002/JLB.4MR1019-189R. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Panel on Antiretroviral Guidelines for Adults and Adolescents . Guidelines for the use of antiretroviral agents in adults and adolescents with HIV. Department of Health and Human Services; 2025. Available from: https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-arv/whats-new. [Last accessed on Oct 16, 2025]. [Google Scholar]
  • 12.Consolidated guidelines on HIV prevention, testing, treatment, service delivery and monitoring: recommendations for a public health approach. World Health Organization, 2021. Available from: https://www.who.int/publications/i/item/9789240031593. [Last accessed on Oct 16, 2025]. [PubMed] [Google Scholar]
  • 13.Lewden C Chene G Morlat P Raffi F Dupon M Dellamonica P, et al. HIV-infected adults with a CD4 cell count greater than 500 cells/mm3 on long-term combination antiretroviral therapy reach same mortality rates as the general population. J Acquir Immune Defic Syndr 2007;46:72-77. doi: 10.1097/QAI.0b013e318134257a. [DOI] [PubMed] [Google Scholar]
  • 14.Engsig FN Zangerle R Katsarou O Dabis F Reiss P Gill J, et al. Long-term mortality in HIV-positive individuals virally suppressed for >3 years with incomplete CD4 recovery. Clin Infect Dis 2014;58:1312-1321. doi: 10.1093/cid/ciu038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lichtenstein KA Armon C Buchacz K Chmiel JS Buckner K Tedaldi EM, et al. Low CD4+ T cell count is a risk factor for cardiovascular disease events in the HIV outpatient study. Clin Infect Dis 2010;51:435-447. doi: 10.1086/655144. [DOI] [PubMed] [Google Scholar]
  • 16.Han WM Ryom L Sabin CA Greenberg L Cavassini M Egle A, et al. Risk of cancer in people with HIV experiencing varying degrees of immune recovery with sustained virological suppression on antiretroviral treatment for more than 2 years: An international, multicentre, observational cohort. Clin Infect Dis 2025;81:e338-e351. doi: 10.1093/cid/ciaf248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Althoff KN Stewart C Humes E Gerace L Boyd C Gebo K, et al. The forecasted prevalence of comorbidities and multimorbidity in people with HIV in the United States through the year 2030: A modeling study. PLoS Med 2024;21:e1004325. doi: 10.1371/journal.pmed.1004325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Shah ASV Stelzle D Lee KK Beck EJ Alam S Clifford S, et al. Global burden of atherosclerotic cardiovascular disease in people living with HIV: Systematic review and meta-analysis. Circulation 2018;138:1100-1112. doi: 10.1161/CIRCULATIONAHA.117.033369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Park LS Tate JP Sigel K Brown ST Crothers K Gibert C, et al. Viral suppression is associated with lower AIDS-defining and non-AIDS-defining cancer incidence in HIV-infected Veterans. Ann Intern Med 2018;169:87-96. doi: 10.7326/M16-2094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Todowede OO, Mianda SZ, Sartorius B. Prevalence of metabolic syndrome among HIV-positive and HIV-negative populations in sub-Saharan Africa: A systematic review and meta-analysis. Syst Rev 2019;8:4. doi: 10.1186/s13643-018-0927-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Peng AT, Huang SH, Lee HY, Wu PY, Kuo HY, Hung CC. Polypharmacy and potential drug-drug interactions among people living with HIV in the era of integrase strand transfer inhibitor-based antiretroviral therapy. Int J Antimicrob Agents 2024;63:107067. doi: 10.1016/j.ijantimicag.2023.107067. [DOI] [PubMed] [Google Scholar]
  • 22.Hoare J, Sevenoaks T, Mtukushe B, Williams T, Heany S, Phillips N. Global systematic review of common mental health disorders in adults living with HIV. Curr HIV/AIDS Rep 2021;18:569-580. doi: 10.1007/s11904-021-00583-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.O’Brien KE, Riddell NE, Gómez-Olivé FX, Rae DE, Scheuermaier K, von Schantz M. Sleep disturbances in HIV infection and their biological basis. Sleep Med Rev 2022;65:101571. doi: 10.1016/j.smrv.2021.101571. [DOI] [PubMed] [Google Scholar]
  • 24.Fukunaga R Pierre P Williams JK Briceno-Robaugh R Kalibala S Peterson M, et al. Prioritizing mental health within HIV and tuberculosis services in PEPFAR. Emerg Infect Dis 2024;30:1-5. doi: 10.3201/eid3004.231726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Han WM Jiamsakul A Salleh NAM Choi JY Huy BV Yunihastuti E, et al. HIV treatment outcomes among people who acquired HIV via injecting drug use in the Asia-Pacific region: A longitudinal cohort study. J Int AIDS Soc 2021;24:e25736. doi: 10.1002/jia2.25736. [DOI] [PMC free article] [PubMed] [Google Scholar]

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