Skip to main content

Clusterization of co-morbidities and multi-morbidities among persons living with HIV: a cross-sectional study



Among people living with HIV (PLWH), the prevalence of non-HIV related co-morbidities is increasing. Aim of the present study is to describe co-morbidity and multi-morbidity, their clustering mode and the potential disease-disease interactions in a cohort of Italian HIV patients.


Cross-sectional analysis conducted by the Coordinamento Italiano per lo Studio di Allergia e Infezioni da HIV (CISAI) on adult subjects attending HIV-outpatient facilities. Non-HIV co-morbidities included: cardiovascular disease, diabetes mellitus, hypertension, oncologic diseases, osteoporosis, probable case of chronic obstructive pulmonary disease (COPD), hepatitis C virus (HCV) infection, psychiatric illness, kidney disease. Multi-morbidity was defined as the presence of two or more co-morbidities.


One thousand and eighty-seven patients were enrolled in the study (mean age 47.9 ± 10.8). One hundred-ninety patients (17.5%) had no co-morbidity, whereas 285 (26.2%) had one condition and 612 (56.3%) were multi-morbid. The most recurrent associations were: 1) dyslipidemia + hypertension (237, 21.8%); 2) dyslipidemia + COPD (188, 17.3%); 3) COPD + HCV-Ab+ (141, 12.9%). Multi-morbidity was associated with older age, higher body mass index, current and former smoking, CDC stage C and longer ART duration.


More than 50% of PLHW were multi-morbid and about 30% had three or more concurrent comorbidities. The identification of common patterns of comorbidities address the combined risks of multiple drug and disease-disease interactions.

Peer Review reports


In recent years, the prevalence of co-morbidities among Persons Living With HIV infection (PLWH) increased, as a consequence of aging, chronic inflammation, systemic immune activation, and long-term exposure to the combination antiretroviral therapy (ART) [1,2,3]. For this reason, PLWH had an increased use of non-antiretroviral drugs as compared to the general population [4]. Higher attention was recently paid to the treatment and the consequences of the main co-morbidities: cardiovascular [5], renal [6], neurocognitive [7, 8], bone disease [9], non-AIDS related cancers [10].

Managing patients with multiple chronic co-morbidities is more challenging than managing those with a single condition. Current HIV guidelines [11] recommend close monitoring of cardiovascular, metabolic, hepatic, renal, and bone health. Investigating common patterns and disease-disease interactions between co-morbidities could support the development of intervention models, improve the management of multi-morbid patients, and provide indication for prevention of multiple comorbidities in PLWH [12].

An important issue is how the co-morbidities associate among them (i.e. clusterization of co-morbidities), because of the implications in terms of disease-disease and drug-drug interactions. In fact, if the therapy recommended for one disease is contraindicated in presence of a concurrent medical condition, the usefulness of clinical practice guidelines is limited. In such a scenario, evidence-based treatment guidelines, designed for single diseases, can lead to serious therapeutic conflicts, due to disease-disease and drug-drug interactions. Management of multi-morbid patients is challenging, especially in emergency conditions.

To provide information on the issue, this cross-sectional study aimed at describing the pattern of co-morbidity and multi-morbidity in age class, their clustering mode and the potential disease-disease interactions in a group of PLWH referring to a network of Italian Infectious Diseases centers.


This study is a cross-sectional analysis of baseline data from a cohort study, conducted by the Coordinamento Italiano per lo Studio di Allergia e Infezioni da HIV (CISAI). Patients analyzed were enrolled in the STOPS-HIV Study cohort, from July 2014 to December 2016: this is an ongoing cohort study including adult (≥18 years old) PLWH attending the participating centers. The participation was almost complete, with more than 99% of patients agreeing to enter the study. In September 2018, in the frame of this study, the Cluster Project collected additional information from clinical records of these patients, in order to investigate co-morbidities present at the time of enrollment.

Non-AIDS/non-HIV co-morbidities considered included: previous cardiovascular disease (pCVD), defined as previous diagnosis of myocardial infarction, stroke, angina pectoris, coronary artery, bypass grafting, angioplasty; diabetes mellitus, diagnosed with laboratory data and drug-tracing criteria [13]; high blood pressure, diagnosed with blood pressure measurement and drug-tracing criteria [14]; history of non-AIDS defining cancers, based on medical history, oncologic follow up and drug-tracing criteria; osteoporosis, based on bone density scan and drug-tracing criteria; clinical probable chronic obstructive pulmonary disease (COPD), based on the presence of at least 3 criteria among current smoking habit, age > 40 years, chronic cough, sputum production and dyspnea [15]; antibodies for hepatitis C (HCV Ab+) coinfection; psychiatric illness, based on medical history, specialist evaluation and drug-tracing criteria; kidney disease, based on estimated glomerular filtration rate (eGFR) < 60 ml/min, calculated according to the Modification of Diet in Renal Disease formula [16]; dyslipidemia, based on serum cholesterol (> 200 mg/dL) and triglycerides (> 150 g/dL) values and drug-tracing criteria [17].

Multi-morbidity was defined as the presence of two or more co-morbidities other than HIV infection. The criterion of two or more chronic conditions has been considered a cut-off score to compare multi-morbid and non multi-morbid groups.

All study participants provided informed consent to participate in the parent study, which was approved by the institutional ethics committee of the coordinating center (July 2014).

The STOPSHIV Study aimed at enrolling 1000 subjects. In the Cluster Project, this sample size was considered adequate in order to obtain a precision of at least 5% for any morbidity with prevalence ranging from 10 to 90%.

Statistical methods. Continuous data are presented as means (and standard deviation, SD), or medians (and interquartile range, IQR), and categorical data as frequency and proportions (%). We compared continuous data using analysis of variance test or Wilcoxon test and categorical data using chi-square statistics. Association between risk factors and multi-morbidity was assessed using the odds ratios (OR) and corresponding 95% Confidence intervals (CI), including in the unconditional logistic regression terms for age and sex. If a variable had less than 5% of missing value they were not included in the analysis. No information was missing in more than 5% of subjects.

We assumed a significance level at a p-value < 0.05. All statistical analyses were conducted using SAS 9.4 (SAS Institute, Inc., Cary, North Carolina).


A total of 1087 patients have been enrolled. 799 (73.5%) were men (mean age 48.6 ± SD 11.1), 288 (26.5%) women (46.0 ± 9.6); overall mean age was 47.9 ± 10.8. Patients were mainly Caucasians (89.2%); the main risk factor for HIV acquisition was heterosexual intercourse (44.7%). Other demographics are shown in Table 1.

Table 1 Characteristics of 1087 patients enrolled in the Cluster Project

One hundred-ninety patients (17.5%) had no co-morbidity, whereas 285 (26.2%) had one condition and 612 (56.3%) were multi-morbid: 25.3% had two co-morbidities, 19.3% three, 8.2% four,3.5% five or more. The most frequent co-morbidity was dyslipidemia (55.3%), followed by hypertension (31.4%), COPD (29.4%), hepatitis C virus (HCV) infection (25.4, 5.5% with detectable HCVRNA), psychiatric illness (10.3%), diagnosis of osteopenia/osteoporosis (10.1%), diabetes (6.1%), and renal impairment (4.8%); 95 (8.7%) subjects had history of non-AIDS-defining cancer. Forty-nine patients (4.5%) had pCVD events. Distribution of comorbidities by age class is shown in Fig. 1.

Fig. 1

Multi-morbidity prevalence by age categories. The following morbidity were included: CVD events, diabetes mellitus, hypertension, dyslipidemia, HCV Ab+, psychiatric illness, osteopenia/osteoporosis, renal impairment

Analyzing the pairs of co-morbidities, the most recurrent associations were: 1) dyslipidemia + hypertension (237, 21.8%); 2) dyslipidemia + COPD (188, 17.3%); 3) COPD + HCV-Ab+ (141, 12.9%). Other frequent associations are shown in Fig. 2.

Fig. 2

Most frequent pairs of comorbidities

When we compared parameters of HIV infections and patients’ characteristics between multi-morbid and non multi-morbid patients, after adjusting for age and sex, we observed that all variables were significantly related with multi-morbidity status, except for CD4 cell count used as a continuous variable (by 100 cells/mm3); being ART naïve was not significantly different between groups, although the proportion of ART naïve patients was lower in the multi-morbid group (Table 2). Multi-morbid patients were older and showed lower nadir CD4 cell count, longer period in ART therapy, and, as expected since these variables were used for comorbidity definition, had higher triglycerides, glycemia, and total cholesterol (Table 2). They were more frequently in CDC stage B and C than in stage A. In a model including age, sex, body mass index (BMI), cigarette smoking, intravenous drug use (IVDU) as risk factor for HIV acquisition, CDC stage, ART duration (by 2 years), and current CD4 < 200 cells/mm3, multi-morbidity was associated to CDC stage, years of ART, and current CD4 count < 200 cells/mm3. In the multivariable analysis, type of ART regimen, whether based on protease inhibitors (PI), non-nucleoside reverse transcriptase inhibitors (NNRTI) or integrase strand transfer inhibitors (INSTI), did not significantly differ between groups.

Table 2 Comparison of patients’ characteristics and parameters of HIV infections, between multi-morbid and non multi-morbid patients. Adjusted odds ratios for risk of multi-morbidity

The main factors associated with multi-morbidity were: age, BMI and smoking with CVD/COPD multi-morbidity; age, smoking, and IVDU with CVD/HCV Ab; smoking and CDC stage with CVD/psychiatric illness; age and CDC stage with CVD/non-AIDS-defining cancer; age, smoking, IVDU and CDC stage with CVD/osteopenia or osteoporosis.

Recombining the co-morbidities in triads (Fig. 3), we observed that the most recurrent ones were: 1) dyslipidemia + hypertension + COPD (71, 6.6%), significantly associated with age (aOR 1.06, 95% CI 1.03–1.09 by 1 year) and BMI (aOR 1.10, 95% CI 1.04–1.16 by 1 point); 2) dyslipidemia + COPD + HCV-Ab+ (69 patients, 6.3%), more frequent in patients with longer ART duration (aOR 1.18, 95% CI 1.08–1.28 by 2 years of treatment); 3) hypertension + COPD + HCV-Ab+ (55, 5.1%), significantly associated with sex (aOR 3.13, 95% CI 1.36–7.22) and years of ART (aOR 1.20, 95% CI 1.10–1.32 by 2 years); 4) dyslipidemia + hypertension + HCV (53, 4.9%), related to BMI (aOR 1.08, 95% CI 1.01–1.15), current smoking (aOR 4.88, 95% CI 1.68–14.10) and ART duration (aOR 1.19, 95% CI 1.08–1.31 by 2 years).

Fig. 3

Most frequent triads of comorbidities

We also had details on drug treatments for dyslipidemia and hypertension. Out of 601 subjects with dyslipidemia, 102 (17.0%) were on statins, and 58 (9.6%) on other lipid-lowering drugs (some patients on both), thus leaving 76.0% of subjects without treatment. Older patients (≥65 years old) were more likely be treated than younger ones (61.5% vs 20.4%, p < 0.0001). Similarly though slightly better, out of 341 patients with high blood pressure, 208 (61.0%) were on antihypertensive drugs and 133 (39.0%) without treatment: 74.1% of hypertensive subjects ≥65 years old were on treatment, versus 58.5% of those aged less than 65 years (p = 0.03).


In our sample of patients attending the HIV-outpatient facilities in the participating centers, we found that most PLHW were multi-morbid and about 30% had three or more concurrent conditions. Besides other known risk factors, shared with the general population, such as age, BMI and cigarette smoking, we found that CDC stage, duration of ART and current CD4 cell count < 200 cells/mm3 were risk factors for multi-morbidity.

As regards the frequency of two or more concurrent medical conditions and their clusterization, data are scarce and difficult to compare, at least partly because of heterogeneous definitions of multi-morbidity [18, 19]. In particular, few studies were performed among PLWH. However, our findings are largely consistent with the results of recent studies [20,21,22].

In a cross-sectional study comparing 208 HIV positive subjects with 208 matched HIV negative controls [20], the frequency of multi-morbidity was higher in the former (63% vs 43%) than in the latter, and associated with duration of HIV and ART. In our sample, multi-morbid patients were about 54%, a lower proportion likely due to the younger age of enrolled subjects, and infection variables (duration of ART and advanced CDC stage) were similarly linked to higher probability of having 2 or more co-morbidities.

Comparing co-morbidity in a large cohort of veterans with and without HIV infection, Goulet et al. [21] found that co-morbidity was the rule (60% in HIV positive veterans), and multi-morbidity was common among those with HIV infection (10%). Patterns of comorbidity differed substantially by HIV status, age, and HIV severity. In multivariable analyses, older HIV-infected veterans were more likely to have substance use disorder and multi-morbidity.

Kim et al. [22] performed a study on a population of PLWH, examining the relationship with obesity and multi-morbidity. They found that prevalence increased with progressive BMI categories. Three multi-morbidity clusters were identified: “Metabolic”; “Behavioral”; and “Substance Use”. Obesity was associated with a higher likelihood of multi-morbidity: consistently, our findings show a higher prevalence of multi-morbidity with higher BMI, even after accounting for potential confounders: this result was led by the positive association between BMI and diabetes, hypertension and dyslipidemia, even if a significant inverse relationship was observed with HCV and osteopenia/osteoporosis.

In Italy, comorbidity prevalence has been evaluated by Guaraldi et al. [23] in a sample of 2854 PLWH: using similar diagnostic criteria, previous CVD event and renal impairment prevalence estimates were largely similar, but we found a much lower proportion of subjects with diabetes (6.1% versus 11.1%) and a higher proportion of hypertensive patients (31.4% versus 22.2%). In our study as well as in Guaraldi et al.’s, age was the main determinant of multi-morbidity, although we did not find a significant detrimental role of being male. This discrepancy may be due to the inclusion of smoking and past IVDU in our analysis: in our sample, both factors were more frequent in men than in women, and had a significant relationship with multi-morbidity. Multi-morbidity prevalence could not be compared between studies as reported, because it depended on considered diseases: however, if we defined multi-morbidity as Guaraldi et al. did, just considering diabetes, bone diseases (although with different definition), renal impairment and hypertension, our prevalence estimate was similar (about 14%).

In Geriatric HIV patients older than 65 years from Italy (GEPPO cohort) multi-morbidity was largely present (64% of cases) [24]. Although patients older than 65 years represented only a small proportion (6.3%) of our sample, we consistently found that multi-morbidity was present in about 76.7% of cases (56/73). Also, we observed that in this subgroup drug treatment for hypertension and dyslipidemia was more frequent than in younger PLWH, probably because the concern for CVD risk overrode the risk of drug-drug interaction, in clinicians’ opinion.

In a recent paper, comorbidities were assessed in PLWH participating in two independent cohorts: POPPY and AGEhIV [12]. Analysis identified 6 patterns among the 1073 POPPY: CVD, sexually transmitted diseases, mental health problems, cancers, metabolic disorders, chest/other infections. The CVD pattern was positively associated with cancer, while the mental health pattern was correlated with all the other patterns In the 598 AGEhIV 6 patterns were identified: CVDs, chest/liver, HIV/AIDS events, mental health/neurological problems, STDs, and general health. The general health pattern was correlated with all the other patterns.

Interestingly, Markun et al. [25] performed a study, including HIV negative subjects, with the aim to identify therapeutic conflicts in emergency department patients with multi-morbidity. In this paper, major therapeutic conflict was defined as a situation where clinical practice guidelines recommended a treatment of a medical condition, that is absolutely contraindicated because of a coexisting condition (for example, a situation where anticoagulation is recommended because of a pulmonary embolism, but at the same time contraindicated because of a co-existing gastrointestinal bleeding). Minor therapeutic conflict was defined as a situation where clinical practice guidelines recommended a treatment of one medical condition, that is relatively contraindicated because of a co-existing condition, but the treatment is possible without adverse effects if certain precautions are taken (for example, a situation where acetylsalicylic acid is recommended because of a vascular disease, but at the same time contraindicated because of a co-existing reflux esophagitis). Among major conflicts they found: cancer requiring chemotherapy or immunosuppression in patients with renal failure, or with cirrhosis at risk of gastrointestinal bleeding; and CVD requiring acetylsalicylic acid or oral anticoagulants in cirrhotic patients with disturbances of coagulation. Among minor conflicts they found: CVD requiring diuretic treatment in patients with renal failure; CVD requiring antihypertensive agents in patients with renal failure or with cirrhosis at risk of gastrointestinal bleeding; CVD in patients requiring beta blockers in patients with asthma. Most of these disease-disease interactions are not infrequent in PLWH, but we are not aware of similar studies among these patients.

We also had information on drug treatment for hypertension and dyslipidemia. In both cases, we noted that these conditions were undertreated, with about 25% of dyslipidemic patients on any lipid-lowering treatments, and 60% of hypertensive subjects on hypotensive drugs, as already observed in samples of Italian patients [26, 27]. These two conditions were part of the most frequent triads of non-AIDS/non-HIV related conditions observed in our study, and as such they remained mostly untreated. This finding may be related both to patients’ reluctance to take other drugs, being subjects to a substantial pill burden for HIV, and to physicians’ concern of potential drug-drug interactions, in the context of the chronic treatment for HIV infection.

Our data evidence that, in spite of mean age lower than 50, co-morbidity was the rule among our PLWH (82%), and that more than 50% of our patients were multi-morbid. Moreover, about 30% of them had three or more chronic non-HIV related conditions, thus confirming recent data provided by other studies in the field [8]. Dyslipidemia was, by far, the most frequent co-morbidity, but potential HCV-related damage is still a concern, mainly in patients with long-lasting co-infection, despite the big efforts under way to cure this condition. In the light of the study of Markun et al. [25], the chronic conditions that appear most at risk for disease-disease interactions are liver disease, renal impairment and cardiovascular diseases. In our experience, both in pairs and in triads they appear frequently associated with other comorbidities, and among them. All the conditions potentially at risk for major and minor disease-disease interactions suggested by Markun [22] (respectively cancer + renal impairment, cancer + liver disease, CVD + liver disease, and CVD + renal impairment, CVD + liver disease, CVD + COPD) were present among our patients, although in different percentages. Not unexpectedly, multi-morbid patients presented higher mean age, worse parameters of HIV infections, more compromised metabolic data and renal function with respect to non multi-morbid ones.

In our study we found that cigarette smoking, a modifiable risk factor, was significantly associated with multi-morbidity. This lifestyle factor is linked to increased morbidity and mortality for both HIV and non-HIV related diseases: tobacco use and HIV together may accelerate the development of chronic obstructive pulmonary disease, lung cancer and death [28, 29], and smoking resulted associated with a higher risk of myocardial infarction in the HIV-infected than in the general population as well [30]. Our findings emphasize the need of smoking cessation strategy, with the expectation of longer life expectancy and better quality of life.

The main limitation of our study is the absence of a control group of HIV-negative subject. Moreover, the investigation aimed at identifying only the potential disease-disease interactions; in particular, we considered all the HCVAb+ patients, regardless of the level of liver decompensation. Similarly, we considered also risk factors for CVD, not only the presence of overt cardiac disease. Even if our objective was not to examine polypharmacy, a further challenge should be to evaluate the impact of disease-disease interactions on polypharmacy and, consequently, on drug-drug interactions. Few studies address the problem of clusterization of chronic non communicable conditions among PLWH and, although other cohorts examined a higher number of patients respect to our experience, data were extracted from diagnosis codes, like ICD-9-CM [21], or from electronic health records [22]. In our study, data were provided by the infectious disease specialists who followed their patients, thus providing more reliable and updated data. As a main strength of this study, we could account for several factors potentially related to multi-morbidity, among infection variables, patients’ characteristics and lifestyle factors, primarily smoking habit.


Considering the aging of PLWH, their persistent exposure to chronic inflammation and the possible effects of HAART, it is mandatory to address the phenomenon of clusterization timely, and to detect all the patients at risk of disease-disease interactions. The evaluation of common patterns of comorbidities in PLWH may help to identify and address the combined risks of major and minor therapeutic conflicts and their potential impact on adverse effects and drug-drug interactions, as we previously evidenced and exemplified. Moreover, this should help to adequate the clinical practice guidelines recommendation to this important example on how the “medicine of complexities” is rapidly emerging in our daily clinical practice.

Availability of data and materials

The dataset analyzed during the current study is available from the corresponding author on reasonable request.



Acquired Immunodeficiency Syndrome


adjusted odds ratio


Antiretroviral therapy


Body mass index


Center for Diseases Control


Confidence interval


Coordinamento Italiano per lo Studio di Allergia e Infezioni da HIV


Chronic obstructive pulmonary disease


Cardiovascular diseases


estimated glomerular filtration rate

HCV Ab+:

antibodies for hepatitis C virus


Human Immunodeficiency Virus


Integrase strand transfer inhibitors


Interquartile range


Intravenous drug use


Non nucleoside reverse transcriptase inhibitors


Odds ratio


Protease inhibitors


Persons living with HIV


previous cardiovascular disease


Standard deviation


  1. 1.

    Krentz HB, Kliewer G, Gill MJ. Changing mortality rates and causes of death for HIV-infected individuals living in southern Alberta, Canada, from 1984 to 2003. HIV Med. 2005;6:99–106.

    CAS  Article  Google Scholar 

  2. 2.

    Grinzstejn B, Luz PM, Pacheco AG, Santos DV, Velasque L, Moreira RI, et al. Changing mortality profile among HIV-infected patients in Rio de Janeiro, Brazil: shifting from AIDS to non-AIDS related conditions in the HAART era. PLoS One. 2013;8:e59768.

    Article  Google Scholar 

  3. 3.

    Ford N, Shubber Z, Meintjes G, Grinsztejn B, Eholie S, Mills EJ, et al. Causes of hospital admission among people living with HIV worldwide: a systematic review and meta-analysis. Lancet HIV. 2015;2:e438–44.

    Article  Google Scholar 

  4. 4.

    Rasmussen LD, Kronborg G, Larsen CS, Pedersen C, Gerstoft J, Obel N, Pottegård A. Use of non-antiretroviral drugs among individuals with and without HIV-infection: a Danish nationwide study. Infect Dis (Lond). 2017;49:42–54. Epub 2016 Aug 11.

    CAS  Article  Google Scholar 

  5. 5.

    Maggi P, Di Biagio A, Rusconi S, Cicalini S, D'Abbraccio M, d'Ettorre G, et al. Cardiovascular risk and dyslipidemia among persons living with HIV: a review. BMC Infect Dis. 2017;17:551.

    Article  Google Scholar 

  6. 6.

    Rasch MG, Engsig FN, Feldt-Rasmussen B, Kirk O, Kronborg G, Pedersen C, et al. Renal function and incidence of chronic kidney disease in HIV patients: a Danish cohort study. Scand J Infect Dis. 2012;44:689–96.

    CAS  Article  Google Scholar 

  7. 7.

    Madsen LW, Fabricius T, Hjerrild S, Hansen TM, Mössner BK, Birkemose I, et al. Depressive symptoms are frequent among drug users, but not associated with hepatitis C infection. Scand J Infect Dis. 2014;46:566–72.

    CAS  Article  Google Scholar 

  8. 8.

    van den Dries LWJ, Wagener MN, Jiskoot LC, Visser M, Robertson KR, Adriani KS, van Gorp ECM. Neurocognitive impairment in a chronically well-suppressed HIV-infected population: the Dutch TREVI cohort study. AIDS Patient Care STDs. 2017;31:329–34.

    Article  Google Scholar 

  9. 9.

    Kruger MJ, Nell TA. Bone mineral density in people living with HIV: a narrative review of the literature. AIDS Res Ther. 2017;14:35.

    CAS  Article  Google Scholar 

  10. 10.

    Ji Y, Lu H. Malignancies in HIV-infected and AIDS patients. Adv Exp Med Biol. 2017;1018:167–79.

    CAS  Article  Google Scholar 

  11. 11.

    European AIDS Clinical Society (EACS) Guidelines. Version 9.1 October 2018. Available online at:

  12. 12.

    De Francesco D, Verboeket SO, Underwood J, Bagkeris E, Wit FW, Mallon PWG, et al. Pharmacokinetic and clinical observations in PeoPle over fiftY (POPPY) study and the AGEhIV cohort study. Patterns of co-occurring comorbidities in people living with HIV. Open Forum Infect Dis. 2018;5:ofy272.

    Article  Google Scholar 

  13. 13.

    American Diabetes Association. Classification and diagnosis of diabetes. Diabetes Care. 2016;39(Supplement 1:S13–22.

    Article  Google Scholar 

  14. 14.

    Mancia G, Fagard R, Narkiewicz K, Redón J, Zanchetti A, Böhm M, et al. Task force members. 2013 ESH/ESC guidelines for the management of arterial hypertension: the task force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC). J Hypertens. 2013;31:1281–357.

    CAS  Article  Google Scholar 

  15. 15.

    Rabe KF, Hurd S, Anzueto A, Barnes PJ, Buist SA, Calverley P, et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Global initiative for chronic obstructive lung disease. Am J Respir Crit Care Med. 2007;176(6):532–55.

    Article  Google Scholar 

  16. 16.

    Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, Roth D. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of diet in renal disease study group. Ann Intern Med. 1999;130:461–70.

    CAS  Article  Google Scholar 

  17. 17.

    National Cholesterol Education. Program detection, evaluation and treatment of high blood cholesterol in adults (adult treatment panel III). Circulation. 2002;106:3143–21.

    Article  Google Scholar 

  18. 18.

    Fortin M, Stewart M, Poitras ME, Almirall J, Maddocks H. A systematic review of prevalence studies on multi-morbidity: toward a more uniform methodology. Ann Fam Med. 2012;10:142–51.

    Article  Google Scholar 

  19. 19.

    Valderas J, Starfield B, Sibbald B, Salisbury C, Roland M. Defining comorbidity: implications for understanding health and health services. Ann Fam Med. 2009;7:357–63.

    Article  Google Scholar 

  20. 20.

    Maciel RA, Klück 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.

    Article  Google Scholar 

  21. 21.

    Goulet JL, Fultz SL, Rimland D, Butt A, Gibert C, Rodriguez-Barradas M, et al. Do patterns of comorbidity vary by HIV status, age, and HIV severity? Clin Infect Dis. 2007;45:1593–601.

    Article  Google Scholar 

  22. 22.

    Kim DJ, Westfall AO, Chamot E, Willig AL, Mugavero MJ, Ritchie C, et al. Multi-morbidity patterns in HIV-infected patients: the role of obesity in chronic disease clustering. J Acquir Immune Defic Syndr. 2012;61:600–5.

    Article  Google Scholar 

  23. 23.

    Guaraldi G, Orlando G, Zona S, Menozzi M, Carli F, Garlassi E, et al. Premature age-related comorbidities among HIV-infected persons compared with the general population. Clin Infect Dis. 2011;53:1120–6.

    Article  Google Scholar 

  24. 24.

    Guaraldi G, Malagoli A, Calcagno A, Mussi C, Celesia BM, Carli F, et al. The increasing burden and complexity of multi-morbidity and polypharmacy in geriatric HIV patients: a cross sectional study of people aged 65 - 74 years and more than 75 years. BMC Geriatr. 2018;18:99.

    CAS  Article  Google Scholar 

  25. 25.

    Markun S, Holzer BM, Rodak R, Kaplan V, Wagner CC, Battegay E, et al. Therapeutic conflicts in emergency department patients with multi-morbidity: a cross sectional study. PLoS One. 2014;9:e110309.

    Article  Google Scholar 

  26. 26.

    De Socio GV, Ricci E, Parruti G, Calza L, Maggi P, Celesia BM, et al. Statins and aspirin use in HIV-infected people: gap between European AIDS clinical society guidelines and clinical practice: the results from HIV-HY study. Infection. 2016;44(5):589–97.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    De Socio GV, Ricci E, Maggi P, Parruti G, Pucci G, Di Biagio A, et al. CISAI study group. Prevalence, awareness, treatment, and control rate of hypertension in HIV-infected patients: the HIV-HY study. Am J Hypertens. 2014;27:222–8.

    Article  Google Scholar 

  28. 28.

    Sigel K, Wisnivesky J, Gordon K, et al. HIV as an independent risk factor for incident lung cancer. AIDS. 2012;26:1017–25.

    Article  Google Scholar 

  29. 29.

    Reddy KP, Kong CY, Hyle EP, et al. Lung Cancer mortality associated with smoking and smoking cessation among people living with HIV in the United States. JAMA Intern Med. 2017;177:1613–21.

    Article  Google Scholar 

  30. 30.

    Rasmussen LD, Helleberg M, May MT, et al. Myocardial infarction among Danish HIV-infected individuals: population-attributable fractions associated with smoking. Clin Infect Dis. 2015;60:1415–23.

    Article  Google Scholar 

Download references


Not applicable.


No funding was obtained for this study.

Author information




Conceptualization: PM and GVDS; Methodology; PM, GVDS and ER; Investigation and data curation: CRS, MN, NDG, CB,ES,GO, BM, NS, DF, ADB, FV, CM, GBG, ADB; Formal analysis: ER; Writing - original draft preparation: PM and GVDSM; Writing – draft revision: PM, PB and GVDS. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Elena Ricci.

Ethics declarations

Ethics approval and consent to participate

The STOPSHIV Project was approved by Comitato Etico Aziende Sanitarie (CEAS) Umbria, Ethics Committee for Azienda Ospedaliera di Perugia and University of Perugia, Santa Maria Hospital, Perugia.

Date and reference number of approval: on July 16th, 2014 (protocol number 3896/14/OV, emended on June 17th, 2015, reference number 5964/15/ESS.

All patients included gave their written informed consent to participate in the study.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Maggi, P., Santoro, C.R., Nofri, M. et al. Clusterization of co-morbidities and multi-morbidities among persons living with HIV: a cross-sectional study. BMC Infect Dis 19, 555 (2019).

Download citation


  • HIV
  • Co-morbidity
  • Multi-morbidity
  • Disease-disease interactions
  • Clusterization