TY - JOUR
T1 - Assessing linear CD4 decline quantifying diagnosis delay after HIV seroconversion
T2 - assessing the linearity assumption of CD4 decline
AU - Robertson, McKaylee M.
AU - Braunstein, Sarah L.
AU - Hoover, Donald R.
AU - Li, Sheng
AU - Nash, Denis
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/12
Y1 - 2020/12
N2 - Purpose: To estimate time from seroconversion to diagnosis, researchers have modeled time based on CD4 decline, assuming the square root of the CD4 count decreases linearly over time before antiretroviral treatment (ART) initiation. If true, utilizing CD4 counts reported anytime in the pre-ART period would result in estimates of diagnosis delay that are not appreciably different. Methods: We applied CD4 depletion model parameters from seroconverter cohorts to New York City residents diagnosed from 2006 to 2015, having two or more pre-ART CD4 counts. Results: Median diagnosis delays based on first or second pre-ART CD4 counts were similar (n = 12,849; 2.8 years, interquartile range [IQR]: 0–7.7, and 2.8 years, IQR: 0–7.6, respectively; P = .09, Wilcoxon signed-rank test). Among people whose second pre-ART CD4 count was measured more than 6 months after diagnosis (n = 2761), the average diagnosis delay based on first pre-ART CD4 count was shorter (1.5 years, IQR: 0–5.4) than the second pre-ART CD4 count (1.7 years, IQR: 0–6.0) but not significantly (P = .12). Conclusions: Results are consistent with the linearity assumption of the CD4 depletion model. To estimate population-level diagnosis delay, researchers may use pre-ART CD4 counts reported more than 6 months post-diagnosis.
AB - Purpose: To estimate time from seroconversion to diagnosis, researchers have modeled time based on CD4 decline, assuming the square root of the CD4 count decreases linearly over time before antiretroviral treatment (ART) initiation. If true, utilizing CD4 counts reported anytime in the pre-ART period would result in estimates of diagnosis delay that are not appreciably different. Methods: We applied CD4 depletion model parameters from seroconverter cohorts to New York City residents diagnosed from 2006 to 2015, having two or more pre-ART CD4 counts. Results: Median diagnosis delays based on first or second pre-ART CD4 counts were similar (n = 12,849; 2.8 years, interquartile range [IQR]: 0–7.7, and 2.8 years, IQR: 0–7.6, respectively; P = .09, Wilcoxon signed-rank test). Among people whose second pre-ART CD4 count was measured more than 6 months after diagnosis (n = 2761), the average diagnosis delay based on first pre-ART CD4 count was shorter (1.5 years, IQR: 0–5.4) than the second pre-ART CD4 count (1.7 years, IQR: 0–6.0) but not significantly (P = .12). Conclusions: Results are consistent with the linearity assumption of the CD4 depletion model. To estimate population-level diagnosis delay, researchers may use pre-ART CD4 counts reported more than 6 months post-diagnosis.
KW - CD4 depletion model
KW - Diagnosis delay
KW - HIV
KW - Incidence
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U2 - 10.1016/j.annepidem.2020.08.003
DO - 10.1016/j.annepidem.2020.08.003
M3 - Article
C2 - 32791198
AN - SCOPUS:85090933790
SN - 1047-2797
VL - 52
SP - 1
EP - 6
JO - Annals of Epidemiology
JF - Annals of Epidemiology
ER -