A comparison of height and weight velocity as a part of the composite endpoint in pediatric HIV

被引:21
作者
Benjamin, DK [1 ]
Miller, WC
Benjamin, DK [1 ]
Ryder, RW
Weber, DJ
Walter, E
McKinney, RE
机构
[1] Duke Clin Res Inst, Durham, NC 27715 USA
[2] Duke Univ, Dept Pediat, Durham, NC 27706 USA
[3] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[4] Univ N Carolina, Dept Med, Chapel Hill, NC 27515 USA
[5] Clemson Univ, Dept Econ, Clemson, SC USA
关键词
children; growth; weight; height; velocity; prediction;
D O I
10.1097/00002030-200311070-00007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: HIV adversely affects growth in children. Pediatric AIDS Clinical Trial Group (PACTG) protocols often use weight velocity [changes in weight z-score for age (WAZ)] as a part of the composite endpoint for phase II and III clinical trials. However, WAZ and height velocity (HAZ) have not been critically compared for their utility as part of the composite endpoint. Methods: HAZ and WAZ were compared to predict laboratory and clinical progression of HIV in a retrospective cohort study of HIV-infected children with data from PACTG Protocol 300. Results: In both bivariable and multivariable analyses, changes in HAZ were more closely linked to subsequent progression than WAZ. Children with improved HAZ were somewhat less likely to exhibit virological failure [odds ratio (OR), 0.76; 95% confidence interval (Cl) 0.51-1.14], than children with improved WAZ (OR, 1.45; 95% Cl, 0.99,2.11). Children who had improved HAZ were less likely to exhibit immunological failure (OR, 0.7; 95% Cl, 0.49-1.00), than children with improved WAZ (OR, 1.13; 95% Cl, 0.82-1.57). Children who had improved HAZ were less likely to have other forms of clinical progression of HIV (OR, 0.55; 95% Cl, 0.31-0.99), than children who had improved WAZ (OR, 1.0; 95% Cl, 1.58-1.94). Conclusions: Increases in HAZ were associated with reduced risk of subsequent clinical progression and subsequent immune reconstitution and weakly associated with declines in HIV RNA. Changes in WAZ were not associated with laboratory outcomes relevant to pediatric HIV infection. Height velocity should be considered as a component of a composite clinical endpoint in future PACTG trials. (C) 2003 Lippincoft Williams Wilkins.
引用
收藏
页码:2331 / 2336
页数:6
相关论文
共 12 条
[1]  
[Anonymous], 1994, Morbidity and Mortality Weekly Report, V43, P1
[2]   Evaluation of pharmacokinetics, safety, tolerance, and activity of combination of zalcitabine and zidovudine in stable, zidovudine-treated pediatric patients with human immunodeficiency virus infection [J].
Bakshi, SS ;
Britto, P ;
Capparelli, E ;
Mofenson, L ;
Fowler, MG ;
Rasheed, S ;
Schoenfeld, D ;
Zimmer, B ;
Frank, Y ;
Yogev, R ;
Jimenez, E ;
Salgo, M ;
Boone, G ;
Pahwa, SG .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (05) :1039-1050
[3]   Randomized study of the tolerance and efficacy of high- versus low-dose zidovudine in human immunodeficiency virus-infected children with mild to moderate symptoms (AIDS Clinical Trials Group 128) [J].
Brady, MT ;
McGrath, N ;
Brouwers, P ;
Gelber, R ;
Fowler, MG ;
Yogev, R ;
Hutton, N ;
Bryson, YJ ;
Mitchell, CD ;
Fikrig, S ;
Borkowsky, W ;
Jimenez, E ;
McSherry, G ;
Rubinstein, A ;
Wilfert, CM ;
McIntosh, K ;
Elkins, MM ;
Weintrub, PS ;
Bernstein, L ;
Shliozberg, J ;
Livingston, RA ;
Vink, P ;
Flautt, L ;
Kline, MW ;
Rayborn, T ;
Kaul, A ;
Lawrence, R ;
Chandwani, S ;
RubinHale, A ;
KnoxBurke, K ;
AlAttar, I ;
Cooper, ER ;
Pelton, SI ;
Regan, AM ;
Damon, B ;
Young, B ;
Nozyce, M ;
Cihak, P ;
Wiznia, A ;
Chadwick, EG ;
Silio, M ;
Klauke, BJ ;
Oleske, JM ;
Colabelli, NB ;
Connor, EM ;
Gershon, A ;
Pitt, J ;
Shea, K ;
Clark, P ;
Cervia, JS .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (05) :1097-1106
[4]   REDUCTION OF MATERNAL-INFANT TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 WITH ZIDOVUDINE TREATMENT [J].
CONNOR, EM ;
SPERLING, RS ;
GELBER, R ;
KISELEV, P ;
SCOTT, G ;
OSULLIVAN, MJ ;
VANDYKE, R ;
BEY, M ;
SHEARER, W ;
JACOBSON, RL ;
JIMENEZ, E ;
ONEILL, E ;
BAZIN, B ;
DELFRAISSY, JF ;
CULNANE, M ;
COOMBS, R ;
ELKINS, M ;
MOYE, J ;
STRATTON, P ;
BALSLEY, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (18) :1173-1180
[5]   Zidovudine, didanosine, or both as the initial treatment for symptomatic HIV-infected children [J].
Englund, JA ;
Baker, CJ ;
Raskino, C ;
McKinney, RE ;
Petrie, B ;
Fowler, MG ;
Pearson, D ;
Gershon, A ;
McSherry, GD ;
Abrams, EJ ;
Schliozberg, J ;
Sullivan, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (24) :1704-1712
[6]  
Kline M W, 1998, J Int Assoc Physicians AIDS Care, V4, P37
[7]   A randomized comparative trial of stavudine (d4T) versus zidovudine (ZDV, AZT) in children with human immunodeficiency virus infection [J].
Kline, MW ;
Van Dyke, RB ;
Lindsey, JC ;
Gwynne, M ;
Culnane, M ;
McKinney, RE ;
Nichols, S ;
Mitchell, WG ;
Yogev, R ;
Hutcheon, N .
PEDIATRICS, 1998, 101 (02) :214-220
[8]   Combination therapy with stavudine (d47) plus didanosine (ddI) in children with human immunodeficiency virus infection [J].
Kline, MW ;
Van Dyke, RB ;
Lindsey, JC ;
Gwynne, M ;
Culnane, M ;
Diaz, C ;
Yogev, R ;
McKinney, RE ;
Abrams, EJ ;
Mofenson, LM .
PEDIATRICS, 1999, 103 (05) :e62
[9]   A randomized study of combined zidovudine-lamivudine versus didanosine monotherapy in children with symptomatic therapy-naive HIV-1 infection [J].
McKinney, RE ;
Johnson, GM ;
Stanley, K ;
Yong, FH ;
Keller, A ;
O'Donnell, KJ ;
Brouwers, P ;
Mitchell, WG ;
Yogev, R ;
Wara, DW ;
Wiznia, A ;
Mofenson, L ;
McNamara, J ;
Spector, SA .
JOURNAL OF PEDIATRICS, 1998, 133 (04) :500-508
[10]  
NACHMAN SA, JAMA, V283, P492