The Effect of Age on Immune System Reconstitution Among HIV-infected Patients on Antiretroviral Therapy in Resource Limited Settings

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The Effect of Age on Immune System Reconstitution Among HIV-infected Patients on Antiretroviral Therapy in Resource Limited Settings Kristen A. Stafford, MPH, PhD, Laurence S. Magder, PhD, Laura L. Hungerford, DVM, MPH, PhD, Jack M. Guralnik, MD, PhD, Samer S. El-Kamary, MB, Ch.B., MPH, Mona Baumgarten, PhD, Robert R. Redfield, MD 7 th International Workshop on HIV & Aging Washington, DC September 27, 2016

Disclosures No conflicts to declare Funding source NIH K-12 HD43489-13 (Building Independent Research Careers in Women s Health)

Overview Background Methods Results Strengths and Limitations Discussion

BACKGROUND

HIV in Adults 50 and Older Sub-Saharan Africa 2011: 3.1 million (13% of the HIV population) 2040: 9.1 million (27% of the HIV population) Change in age distribution is a result of Increased life expectancy due to antiretroviral therapy New infections among older adults Hontelez, 2012 AIDS.

Importance Most studies of HIV in older adults are from the US and Europe Immunologic response to ART may differ in sub-saharan Africa Higher levels of immune activation due to nutritional deficiencies, endemic parasitic, helminth, and bacterial infections Studies of immune response in resource limited settings have mostly been limited to 12 months after ART start Need to assess whether the association between age and CD4 cell gain differs by level of baseline immunosuppression

Moore and Keruly 2007, CID

Age and Immune Response Studies from the US and Europe Moderately lower immune response in older compared to younger patients (25 cells) No clear age threshold identified Studies from resource limited settings Moderately lower immune response (22 cells) Two smaller studies No effect of age Grabar 2004, AIDS; Nogueras 2006 BMC ID; Moore 2007, CID Balestre 2010, AIDS; Mutevedzi 2011, PLOS ONE; Eduardo 2014, PLOS ONE Tumbarello 2004, BMC ID; Orlando 2006, HIV Med

METHODS

UMB-IHV was the medical lead in a five member consortium with Catholic Relief Services as the prime grantee Technical assistance and training Medical Nursing Laboratory Community Based Treatment Services Program Evaluation and Quality Improvement Eight countries, 270 clinics, 700,000 people

Design Retrospective open cohort Adults who initiated ART August 1, 2004 and September 1, 2012 157 PEPFAR funded and AIDSRelief supported facilities Kenya, Nigeria, Tanzania, and Uganda

Study Sample Eligibility criteria HIV positive 20 years of age or older Initiated ART during the study period No previous ART exposure including singledose nevirapine 452,819 ever enrolled 158,160 eligible

Analyses for Statistical Inference Random effects linear models Heterogeneous Toeplitz covariance structure Created by adding one variable at a time and assessing changes in the beta estimate for the exposure outcome association, Akaike s information criterion, and -2 log likelihood Mediation analysis for effect of medication adherence

Aim Estimate the association between age at start of treatment and the mean CD4 cell count at six month intervals after initiation of cart

Results Median age (IQR) Median CD4 (IQR) Baseline CD4 strata, n (%) 20 29 (n=38,854) 30 39 (n=63,220) 40 49 (n=36,959) 50 59 (n=14,102) 60 (n=5,025) 26 (24 28) 35 (32 39) 44 (42 47) 53 (51 56) 64 (61 68) 197 (97 298) 170 (80 270) 169 (83 266) 176 (91 273) 182 (97 277) 200 16,054 (41) 29,550 (47) 17,377 (47) 6,420 (46) 2,227 (44) 201 350 11,239 (29) 16,282 (26) 9,596 (26) 3,822 (27) 1,445 (29) > 350 4,149 (11) 4,680 (7) 2,462 (7) 986 (7) 338 (7) Missing 7,412 (19) 12,708 (20) 7,524 (20) 2,874 (20) 1,015 (20)

Adjusted * mean CD4 cell count among patients started on ART with a baseline CD4 cell count 200 by age group * Adjusted for sex, WHO stage, functional status, ART regimen, TB, and other OIs

Adjusted * mean CD4 cell count among patients started on ART with a baseline CD4 cell count of 201 350 by age group * Adjusted for sex, WHO stage, functional status, ART regimen, TB, and other OIs

Adjusted * mean CD4 cell count among patients started on ART with a baseline CD4 cell count of > 350 by age group * Adjusted for sex, WHO stage, functional status, ART regimen, TB, and other OIs

Age Group Mean Difference Over Time Compared to Patients Age 20 29 at ART Start with a baseline CD4 cell count 200 cells/mm 3 Months 0 6 12 18 24 30 36 42 48 20 29 Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. 30 39 0-21 -24-28 -24-24 -26-24 2 40 49 9-29 -32-37 -35-31 -36-31 -23 50 59 15-18 -29-36 -37-43 -44-40 -35 60+ 21-18 -22-49 -49-61 -68-53 -63

Age Group Mean Difference Over Time Compared to Patients Age 20 29 at ART Start with a baseline CD4 cell count between 201 350 cells/mm 3 Months 0 6 12 18 24 30 36 42 48 20 29 Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. 30 39 2-32 -32-44 -44-40 -42-31 -40 40 49 4-44 -41-52 -57-45 -55-36 -51 50 59 6-48 -53-65 -68-59 -58-61 -48 60+ 10-52 -77-82 -92-90 -97-109 -76

Age Group Mean Difference Over Time Compared to Patients Age 20 29 at ART Start with a baseline CD4 cell count > 350 cells/mm 3 Months 0 6 12 18 24 30 36 42 48 20 29 Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. Ref. 30 39-1 -66-73 -46-50 -57-55 -28-59 40 49-10 -89-109 -82-64 -85-95 -31-51 50 59-1 -96-87 -82-53 -80-108 -65-48 60+ -7-89 -85-91 -154-104 -73-114 -74

STRENGTHS & LIMITATIONS

Up and Down Sides Down side Data was collected for routine care, not research Probably more missing and incorrect data than in a prospectively designed study Missing information on some important confounders (duration of HIV infection, VL) Selection bias due to death and loss to follow-up Frequency of both was low in this study population (9% and 8%) Upside Sensitivity analysis yielded similar and slightly larger differences by age and CD4 strata Methods used may explain why other studies found only moderate differences Follow-up was well beyond the first 12 months where differences tend to be smallest

DISCUSSION

Summary Mean CD4 cell count differs over time by age within CD4 strata The size of the differences at lower levels of baseline CD4 cell count may not be clinically relevant Over time they translate to staying at risk for certain infections longer Among patients starting ART with a CD4 between 201 and 350 cells/mm 3, differences increase with age and are clinically meaningful Delays in achieving same level of immune reconstitution are more pronounced While large differences were observed in the highest strata of baseline CD4, it is unclear if these differences reflect a clinical disadvantage among older adults

Conclusion The removal of CD4 thresholds for the initiation of ART in resource limited settings has the potential to mitigate clinically meaningful age related differences in CD4 cell reconstitution 50 may not be the appropriate cut off for older individuals living with HIV in resource limited settings

Thank You AIDSRelief Patients and staff of the AR clinics AR partners Catholic Relief Services Futures Group International Catholic Medical Mission Board IMA World Health Co-authors Dr. Mona Baumgarten Dr. Samer El-Kamary Dr. Jack Guralnik Dr. Laura Hungerford Dr. Laurence Magder Dr. Robert Redfield

Why Stratify by Baseline CD4 Controlling for baseline CD4 cell count estimates a constant mean difference over time by CD4 category The effect of other covariates may differ at different levels of baseline CD4 Male sex -43 at 200, -25 at 201 350, -51 at >350, -24 in a model controlling for CD4 TB -28 at 200, -15 at 201-350, -4 at >350, - 9 in a model controlling for CD4

Mean CD4 cell count controlling for baseline CD4 by age 700 600 500 CD4 cells/mm 3 400 300 200 100 0 0 6 12 18 24 30 36 42 48 54 60 Months after ART start 20-29 30-39 40-49 50-59 60+