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All-cause mortality in the cohorts of the Spanish AIDS Research Network (RIS) compared with the general population: 1997–2010

  • Victoria Hernando1, 2Email author,
  • Belen Alejos1, 2,
  • Susana Monge1, 2,
  • Juan Berenguer3,
  • Lourdes Anta4,
  • David Vinuesa5,
  • Rosario Palacios6,
  • Roberto Muga7,
  • Santiago Moreno8,
  • Inma Jarrin1, 2 and
  • CoRIS cohort
BMC Infectious Diseases201313:382

https://doi.org/10.1186/1471-2334-13-382

Received: 19 February 2013

Accepted: 6 August 2013

Published: 20 August 2013

Abstract

Background

Combination antiretroviral therapy (cART) has produced significant changes in mortality of HIV-infected persons. Our objective was to estimate mortality rates, standardized mortality ratios and excess mortality rates of cohorts of the AIDS Research Network (RIS) (CoRIS-MD and CoRIS) compared to the general population.

Methods

We analysed data of CoRIS-MD and CoRIS cohorts from 1997 to 2010. We calculated: (i) all-cause mortality rates, (ii) standardized mortality ratio (SMR) and (iii) excess mortality rates for both cohort for 100 person-years (py) of follow-up, comparing all-cause mortality with that of the general population of similar age and gender.

Results

Between 1997 and 2010, 8,214 HIV positive subjects were included, 2,453 (29.9%) in CoRIS-MD and 5,761 (70.1%) in CoRIS and 294 deaths were registered. All-cause mortality rate was 1.02 (95% CI 0.91-1.15) per 100 py, SMR was 6.8 (95% CI 5.9-7.9) and excess mortality rate was 0.8 (95% CI 0.7-0.9) per 100 py. Mortality was higher in patients with AIDS, hepatitis C virus (HCV) co-infection, and those from CoRIS-MD cohort (1997–2003).

Conclusion

Mortality among HIV-positive persons remains higher than that of the general population of similar age and sex, with significant differences depending on the history of AIDS or HCV coinfection.

Keywords

Mortality rate HIV infection Standardized mortality ratios Excess mortality

Background

Mortality of HIV-infected persons in Western countries has decreased significantly due to improvements in combined antiretroviral therapy (cART) [1, 2]. Nevertheless it continues to be higher than in the general population [35], even in HIV-infected patients with good initial response to cART [6]. Global reduction in mortality has been achieved thanks to a decrease of AIDS-related deaths which has led to a greater relevance of other causes of death in relation to co-morbidities, such as hepatitis C virus (HCV) and/or hepatitis B virus (HBV) co-infections, drug abuse and cardiovascular diseases [2, 7].

In Barcelona and Navarre, HIV-positive subjects were found to have a higher mortality compared to the general population [8, 9] but no estimates are available for the whole country. Unlike other cohorts, in this work we have analyzed data of a cohort of persons with HIV infection recruited during a period where highly effective antiretroviral treatment is available and all patients are naïve to treatment. But we believe that even though these patients may be in a better starting point than patients in other similar studies, the risk of mortality compared with the general population is still higher.

Therefore, the objectives of this study were to calculate the overall mortality rates, standardized mortality ratios (SMR), and excess mortality rates in the cohorts of the Spanish AIDS Research Network (RIS) – CoRIS-MD and CoRIS, comparing the overall mortality rates observed in HIV positive subjects in both cohorts with the mortality rates of the general population of similar age and sex.

Methods

Patients

We analyzed data from the cohorts of HIV-infected adults of the Spanish AIDS Research Network (RIS). CoRIS-MD is a multicenter cohort including data from 1997 to 2003 from 9 hospitals of 7 Spanish Autonomous regions assembled in 2003. CoRIS is a multicenter cohort which recruits patients from 2004 onwards from 28 health-care centers and hospitals in 12 of the 17 Autonomous regions that compose Spain [10, 11]. Both cohorts recruit patients newly attended in any of the participating sites. Ethics approval was obtained from all hospitals Ethics’ Committees (see Appendix 1 all hospitals participants) and every patient provides written informed consent to participate in the cohorts. For this analysis, we selected subjects who were naïve to cART at cohort entry, older than 20 years, had a follow up of more than 6 months and had had at least one diagnostic test for hepatitis C virus.

Variables

We considered the following variables: age at cohort entry (20–29; 30–39; 40–49; > = 50); gender (male, female); year of cohort entry; HIV transmission category, classified as injecting drugs users (IDUs), men who have sex with men (MSM), heterosexual contact and others or unknown risk category; AIDS before entry and changes in AIDS status during follow-up; CD4 count at entry (<200, 200–349, ≥350); HIV viral load at entry (<20000, 20000–100000, ≥100000); combined antiretroviral treatment (cART) initiation during follow-up; HCV serological status classified as positive or negative antibodies and vital status.

To calculate mortality rates, AIDS variable was classified as “Yes” when the person had AIDS before entering the cohort, AIDS at cohort entry or AIDS during follow-up and “No” when the person didn’t develop AIDS at any moment during the study.

Statistical analyses

Descriptive analysis of patients’ characteristics was carried out using frequency distribution for categorical variables and median (interquartile range -IQR) for continuous variables.

Individuals were followed up from study entry to death, last study contact or the administrative censoring date (31/12/2003 in CoRIS-MD and 31/12/2010 in CoRIS) whichever arose first. We calculated mortality rates, overall and according to socio-demographic and clinical characteristics, as the number of deaths by 100 persons-year (py) of follow-up with 95% confidence intervals (95% CI) calculated using the exact Poisson method.

Standardized mortality ratios (SMR) were estimated for all-cause mortality in CoRIS-MD and CoRIS, comparing with the overall mortality rates of the general population standardized by sex and age. SMR were estimated as the ratio of observed deaths to expected deaths, had our patients had the same distribution of mortality as the general population. SMR were calculated through Poisson models offsetting expected mortality rates, and adjusted for gender, age, category of transmission and HCV test. Mortality rates for general population, between 1997 and 2010, were obtained from the National Statistics Institute (http://www.ine.es), stratified by sex and age at 5 year intervals. A constant mortality rate within each 5 year stratum was assumed.

A sensitivity analysis was performed to assess a possible selection bias. The SMR was calculated for the first 12 months after cohort entry separately for all patients together. This was to determinate whether it is necessary to include a lag time to avoid an overestimation of SMR.

Excess Mortality Rates were calculated as the difference between observed and expected deaths according to mortality in the general population, divided by the number of persons-year (py) of follow-up. Confidence intervals for Excess Mortality Rates were estimated using Poisson’s exact method.

All statistical analyses were performed by using Stata software (Version 11.0, College Station, Texas).

Results

Baseline characteristics of the study population

A total of 8,214 subjects were included in the study, 2,453 (29.9%) in CoRIS-MD and 5,761 (70.1%) in CoRIS, adding up to 28,743 persons-year of follow up, and 294 deaths.

Men represented 78.0% (n = 6,412) of the sample, and median age at the cohort entry was 35.0 years (interquartile range IQR: 30.2 – 41.0), 35.5 years (IQR: 30.2-41.7) for men and 34.2 years (IQR: 29.1-40.1) for women. Regarding transmission categories, the sample was distributed between injecting drugs users (IDUs) or ex-users, 25.0% (n = 2,050), men who have sex with men (MSM), 39.6% (n = 3,255), and heterosexuals, 30.7% (n = 2,524). A 20.4% of the subjects had a history of an AIDS defining illness (ADI), although for 59.4% (n = 994) of them the ADI diagnosis was previous to cohort entry. Median CD4 count at cohort entry was 350 cell/mm3 (IQR 170 – 552), and median viral load was 39,811 copies/ml (IQR 7,520 – 135,988) (Table 1).
Table 1

Socio demographics and clinical characteristics at cohort entry for total of analyzed subjects and deceased subjects

  

Total

Deaths

 

py

n

%

n

%

Total

28,743

8,214

100

294

100

Gender

 Males

21,903

6,412

78.0

237

80.6

 Females

6,840

1,802

22.0

57

19.4

Age at cohort entry (years)

 20–29

6,945

2,064

25.1

34

11.6

 30–39

13,778

3,722

45.3

145

49.3

 40–49

5,584

1,705

13.1

71

24.1

 > = 50

2,436

723

8.8

44

15.0

 Median age (IQR)

 

35.0 (30.2–41.0)

37.7(33.5–44.5)

Category of transmission

 IDUs

8,515

2,050

25.0

177

60.2

 MSM

9,994

3,255

39.6

41

14.0

 Heterosexual

8,909

2,524

30.7

67

22.8

 Others/Unknown

1,325

385

4.7

9

3.0

AIDS

 No

22,255

6,542

79.6

144

49.0

 AIDS before entry

3,667

994

12.1

72

24.5

 AIDS after entry

2,821

678

8.3

78

26.5

CD4 count at entry (cel/mm3)

 <200

7,525

2,217

27.0

141

48.0

 200–349

5,191

1,567

19.1

39

13.3

 > = 350

12,366

3,744

45.6

64

21.8

 Unknown

3,661

686

8.4

50

17.0

 Median (IQR)

 

350 (170–552)

154 (66–390)

HIV viral load (copies/ml)

 <20.000

8,748

2,769

33.7

61

20.7

 20.000-100.000

7,141

2,202

26.8

65

22.1

 >100.000

7,181

2,196

26.7

89

30.3

 Unknown

5,673

1,047

12.8

79

26.9

 Median (IQR)

 

39,810 (7,520–135,988)

78,200 (17,335–230,000)

Cohorts

 CoRIS (2004–2008)

18,447

5,761

70.1

137

46.6

 CoRIS-MD (1997–2003)

10,296

2,453

29.9

157

53.4

HCV test

 Negative

18,332

5,673

69.1

96

32.6

 Positive

10,411

2,541

30.9

198

67.4

Antiretroviral treatment during follow-up

 No

9,992

1,948

23.7

63

21.4

 Yes

18,751

6,266

76.3

231

78.6

IDUs Injecting Drugs Users, MSM Men have Sex with Men, HCV Hepatitis C virus.

Among the 294 deceased subjects, 80.6% (n = 237) were men, and median age was 37.7 years (IQR 33.3 – 44.5). Some 60.2% (n = 177) were IDU or ex-IDU, 51.0% (n = 150) had an AIDS diagnosis and 67.4% (n = 198) were co-infected by HCV. Median CD4 count at entry was 154 cell/mm3 (IQR 66 – 390) and median HIV viral load was 78,200 copies/ml (IQR 17,335 – 230,000) (Table 1).

Mortality rates, standardized mortality ratios and excess mortality rates

Figure 1 shows mortality rates for 100 persons-year (py) of follow up, standardized mortality ratios and excess mortality rates for 100 py in both RIS cohorts.
Figure 1

Mortality rates per 100 person-years of follow-up, Standardized mortality ratio (SMRs) and excess mortality rates per 100 person-years of follow-up according to sociodemographic, epidemiological and clinical characteristics.

Overall mortality rate was 1.02 (95% CI: 0.91-1.15) deaths for 100 py of follow up, higher for men (1.08; 95% CI: 0.95-1.23), for subjects over 50 years-old (1.81; 95% CI: 1.34-2.42), for IDU (2.08; 95% CI: 1.79-2.41) compared to both MSM (0.41; 95% CI: 0.30-0.56) and heterosexuals (0.75; 95% CI: 0.59-0.96) and for patients included in CoRIS-MD (1.52; 95% CI: 1.30-1.78). For patients who had an AIDS diagnosis, mortality rate was 2.06 (95% CI: 2.21-3.05), compared to 0.63 (95% CI: 0.54-0.74) for those who were AIDS-free. For HCV co-infected patients mortality rate rose up to 1.90 (95% CI: 1.65-2.19) in contrast with 0.52 (95% CI: 0.42-0.64) for those not co-infected.

Global mortality in both CoRIS cohorts was 6.8 (95% CI: 5.9-7.9) times higher than mortality of the general population of same age and sex. As opposed to the crude mortality rates, standardized mortality ratios were higher in women (10.5; 95% CI: 7.6-13.3) compared to men (5.6; 95% CI: 4.8-6.4). Still, a higher SMR was found for IDUs (9.7; 95% CI: 7.4-12.0), persons with an AIDS diagnosis (14.9; 95% CI: 12.0-17.9), persons co-infected with HCV (9.2; 95% CI: 7.1-11.2) and those receiving antiretroviral treatment (8.1; 95% CI: 6.8-9.4).

In the sensitivity analysis, considering only the first 12 month of follow-up, SMR is lower than in the complete analysis (4.0; 95% CI 2.4 -5.6).

Finally, regarding excess mortality rate, as an absolute estimator, results are similar to those observed for crude mortality rates (Figure 1).

Discussion and conclusion

Our results show that all-cause mortality in CoRIS-MD and CoRIS cohorts, between 1997 and 2010, is close to seven times higher than that of the general population of the same age and sex. Significant differences have been found depending on the history of AIDS and HCV co-infection.

A previously published study, carried out in similar cohorts in Europe and North America, found a lower global SMR, of 3.36 (95% CI: 3.16 – 3.56), but with a notable heterogeneity between cohorts depending on participant-specific characteristics, and being higher for cohorts with a greater representation of IDUs [12]. For example, Aldaz et al. found mortality of HIV-infected persons in Navarre (Spain) to be 14 times higher than mortality in general population; 63% of this cohort had been infected through the use of injected drugs [8].

These differences could also be related to the higher prevalence of HCV-co-infection as the standardized mortality in HCV co-infected subjects in our study was 9.2 times higher than the general population’s. Similar results were found by Lewden et al., where SMR for HCV co-infected persons were 13.9 compared to 4.4 for the HCV negative subjects [4]. In a previous study of CoRIS-MD and CoRIS cohorts, an important increase of the risk of both all cause mortality and liver-related mortality was observed for HIV patients coinfected with HCV [13]. Berenguer et al. also found a decrease in overall mortality in HIV patients in cART era, but only in HCV negative subjects [14] and Chen et al. in a meta-analysis found that the risk of mortality was increased in HCV/HIV coinfected patients in HAART era [15].

In our study, we found a similar SMR for patients recruited in CoRIS, from 2004 onwards, and those recruited in CoRIS-MD, from 1997 to 2003, after adjustment for gender, age, transmission category and HCV infection. That is, the difference in the subject’s characteristics along these years, the decrease in the representation of IDUs and the percentage of HCV co-infected subjects [11, 16, 17] were corrected after adjustment. Others studies observed a lower mortality in recent years with the improvement in antiretroviral therapies [1821], although when specific groups were analyzed, for example: IDUs, found that mortality risk remain elevated [21].

We found non-statistically significant, lower mortality rates in women compared to men. Eventhough the women in our study showed a mortality ratio 10.5 times higher than women of the same age from the general population, and almost doubled the one from men in the cohorts. This higher relative mortality in women could be explained by the fact that women in the general population have a higher life expectancy than men, and specifically, mortality in the general population is very low in women between ages 30 to 40, where we find the majority of HIV-infected women [22]. The lower excess mortality rate in women is consistent with the higher proportion of HIV-infected men in the Spanish epidemic, and in our cohorts [23].

A possible limitation in the calculation of SMR could be using mortality rates in the general population to calculate the expected deaths, because this population contains HIV-related deaths. In our analysis, HIV-related mortality represents a small proportion of all-cause mortality in the general population of Spain, so therefore we consider correct to use the general population mortality rates to calculate the mortality rates in a non-HIV infected population.

The sensitivity analysis shows that when we establish as inclusion criteria to have at least 6 months of follow-up, we are introducing a time window to avoid the selection bias indirectly and overestimate SMRs.

To conclude, mortality in HIV-infected persons continues to be higher than that of the general population, although it has decreased in recent years. For future studies, we would highly recommend to consider, along with global mortality, excess mortality rate for specific causes of death, such as hepatic, non-aids related malignancies or drug-related, especially among IDUs.

Appendix 1: Centers and investigators involved in CoRIS

Executive committee: Juan Berenguer, Julia del Amo, Federico García, Félix Gutiérrez, Pablo Labarga, Santiago Moreno y María Ángeles Muñoz.

Fieldwork, data management and analysis: Paz Sobrino Vegas, Victoria Hernando Sebastián, Belén Alejos Ferreras, Débora Álvarez del Arco, Susana Monge Corella, Inma Jarrín Vera, Adela Castelló.

BioBank: M Ángeles Muñoz-Fernández, Isabel García-Merino, Coral Gómez Rico, Jorge Gallego de la Fuente and Almudena García Torre.

Participating centres:

Hospital General Universitario de Alicante (Alicante): Joaquín Portilla Sogorb, Esperanza Merino de Lucas, Sergio Reus Bañuls, Vicente Boix Martínez, Livia Giner Oncina, Carmen Gadea Pastor, Irene Portilla Tamarit, Patricia Arcaina Toledo.

Hospital Universitario de Canarias (Santa Cruz de Tenerife): Juan Luis Gómez Sirvent, Patricia Rodríguez Fortúnez, María Remedios Alemán Valls, María del Mar Alonso Socas, Ana María López Lirola, María Inmaculada Hernández Hernández, Felicitas Díaz-Flores.

Hospital Carlos III (Madrid): Vicente Soriano, Pablo Labarga, Pablo Barreiro, Pablo Rivas, Francisco Blanco, Luz Martín Carbonero, Eugenia Vispo, Carmen Solera.

Hospital Universitario Central de Asturias (Oviedo): Victor Asensi, Eulalia Valle, José Antonio Cartón

Hospital Clinic (Barcelona): José M. Miró, María López-Dieguez, Christian Manzardo, Laura Zamora, Iñaki Pérez, Mª Teresa García, Carmen Ligero, José Luis Blanco, Felipe García-Alcaide, Esteban Martínez, Josep Mallolas, José M. Gatell.

Hospital Doce de Octubre (Madrid): Rafael Rubio, Federico Pulido, Silvana Fiorante, Jara Llenas, Violeta Rodríguez, Mariano Matarranz.

Hospital Donostia (San Sebastián): José Antonio Iribarren, Julio Arrizabalaga, María José Aramburu, Xabier Camino, Francisco Rodríguez-Arrondo, Miguel Ángel von Wichmann, Lidia Pascual Tomé, Miguel Ángel Goenaga, Mª Jesús Bustinduy, Harkaitz Azkune Galparsoro.

Hospital General Universitario de Elche (Elche): Félix Gutiérrez, Mar Masiá, Cristina López Rodríguez, Sergio Padilla, Andrés Navarro, Fernando Montolio, Catalina Robledano García, Joan Gregori Colomé.

Hospital Germans Trías i Pujol (Badalona): Bonaventura Clotet, Cristina Tural, Lidia Ruiz, Cristina Miranda, Roberto Muga, Jordi Tor, Arantza Sanvisens.

Hospital General Universitario Gregorio Marañón (Madrid): Juan Berenguer, Juan Carlos López Bernaldo de Quirós, Pilar Miralles, Jaime Cosín Ochaíta, Isabel Gutiérrez Cuellar, Margarita Ramírez Schacke, Belén Padilla Ortega, Paloma Gijón Vidaurreta, Ana Carrero Gras, Teresa Aldamiz-Echevarría Lois y Francisco Tejerina Picado.

Hospital Universitari de Tarragona Joan XXIII, IISPV, Universitat Rovira i Virgili (Tarragona): Francesc Vidal, Joaquín Peraire, Consuelo Viladés, Sergio Veloso, Montserrat Vargas, Miguel López-Dupla, Montserrat Olona, Alba Aguilar, Joan Josep Sirvent, Verónica Alba, Olga Calavia.

Hospital Universitario La Fe (Valencia): José López Aldeguer, Marino Blanes Juliá, José Lacruz Rodrigo, Miguel Salavert, Marta Montero, Eva Calabuig, Sandra Cuéllar.

Hospital Universitario La Paz (Madrid): Juan González García, Ignacio Bernardino de la Serna, José Ramón Arribas López, María Luisa Montes Ramírez, Jose Mª Peña, Blanca Arribas, Juan Miguel Castro, Fco Javier Zamora Vargas, Ignacio Pérez Valero, Miriam Estébanez, Silvia García Bujalance, Marta Díaz.

Hospital de la Princesa (Madrid): Ignacio de los Santos, Jesús Sanz Sanz, Ana Salas Aparicio, Cristina Sarriá Cepeda.

Hospital San Pedro-CIBIR (Logroño): José Antonio Oteo, José Ramón Blanco, Valvanera Ibarra, Luis Metola, Mercedes Sanz, Laura Pérez-Martínez.

Hospital San Pedro II (Logroño): Javier Pinilla Moraza.

Hospital Universitario Mutua de Terrassa (Terrassa): David Dalmau, Angels Jaén Manzanera, Mireia Cairó Llobell, Daniel Irigoyen Puig, Laura Ibáñez, Queralt Jordano Montañez, Mariona Xercavins Valls, Javier Martinez-Lacasa, Pablo Velli, Roser Font.

Hospital de Navarra (Pamplona): María Rivero, Marina Itziar Casado, Jorge Alberto Díaz González, Javier Uriz, Jesús Repáraz, Carmen Irigoyen, María Jesús Arraiza.

Hospital Parc Taulí (Sabadell): Ferrán Segura, María José Amengual, Eva Penelo, Gemma Navarro, Montserrat Sala, Manuel Cervantes, Valentín Pineda.

Hospital Ramón y Cajal (Madrid): Santiago Moreno, José Luis Casado, Fernando Dronda, Ana Moreno, María Jesús Pérez Elías, Dolores López, Carolina Gutiérrez, Beatriz Hernández, María Pumares, Paloma Martí.

Hospital Reina Sofía (Murcia): Alfredo Cano Sánchez, Enrique Bernal Morell, Ángeles Muñoz Pérez.

Hospital San Cecilio (Granada): Federico García García, José Hernández Quero, Alejandro Peña Monje, Leopoldo Muñoz Medina, Jorge Parra Ruiz.

Centro Sanitario Sandoval (Madrid): Jorge Del Romero Guerrero, Carmen Rodríguez Martín, Teresa Puerta López, Juan Carlos Carrió Montiel, Cristina González, Mar Vera.

Hospital Universitario Santiago de Compostela (Santiago de Compostela): Antonio Antela, Arturo Prieto, Elena Losada.

Hospital Son Espases (Palma de Mallorca): Melchor Riera, Javier Murillas, Maria Peñaranda, Maria Leyes, Mª Angels Ribas, Antoni Campins, Concepcion Villalonga, Carmen Vidal.

Hospital Universitario de Valme (Sevilla): Juan Antonio Pineda, Eva Recio Sánchez, Fernando Lozano de León, Juan Macías, José del Valle, Jesús Gómez-Mateos.

Hospital Virgen de la Victoria (Málaga): Jesús Santos González, Manuel Márquez Solero, Isabel Viciana Ramos, Rosario Palacios Muñoz.

Hospital Universitario Virgen del Rocío (Sevilla): Pompeyo Viciana, Manuel Leal, Luis Fernando López-Cortés, Mónica Trastoy.

Declarations

Acknowledgments

This study would not have been possible without the collaboration of all the patients, medical and nursing staff, and data mangers who have taken part in the project. The RIS cohort (CoRIS) is funded by the Instituto de Salud Carlos III through the Red Temática de Investigación Cooperativa en sida (RIS C03/173).

Financial support

This work has been partially funded by a grant from the FIS (Spanish Networks for Research on AIDS and Public Health), 04/0900 and RIS (Spanish HIV Research Network for excellence) RD06/0006. Susana Monge has been granted by Rio Ortega program (º exp CM10/00154).

Authors’ Affiliations

(1)
Red de Investigación en Sida, Centro Nacional de Epidemiología, Instituto de Salud Carlos III
(2)
CIBER de Epidemiología y Salud Pública (CIBERESP)
(3)
Hospital Universitario Gregorio Marañón
(4)
Hospital Universitario Carlos III
(5)
Hospital Universitario San Cecilio
(6)
Hospital Universitario Virgen de la Victoria
(7)
Hospital Universitario Germans Trias I Pujol
(8)
Hospital Universitario Ramon y Cajal

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  24. Pre-publication history

    1. The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/13/382/prepub

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