BIRTH-ORDER, DELIVERY ROUTE, AND CONCORDANCE IN THE TRANSMISSION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 FROM MOTHERS TO TWINS

被引:90
作者
DULIEGE, AM
AMOS, CI
FELTON, S
BIGGAR, RJ
ZIEGLER, J
CRUIKSHANK, M
LEVY, J
MEATES, MA
GIBB, D
MAYAUX, MJ
TEGLAS, JP
LAURENT, C
BLANCHE, S
ROUZIOUX, C
HELLINGGIESE, G
MATTNER, U
HOEGER, PH
CONLON, T
GRIFFIN, E
DEMARIA, A
BENEDETTO, A
PRINCIPI, N
GIAQUINTO, C
GIANCOMELLI, A
MOK, J
CASABONA, J
FORTUNY, C
URIZ, S
PEREZ, JM
TUSETRUIZ, MC
LEON, P
ELORZA, JFY
CANOSA, C
BRANDLE, B
SEGER, R
NADAL, D
IRION, O
WYLER, CA
DAVIS, P
LALLEMANT, M
LALLEMANTLECOEUR, S
HITIMANA, DG
LEPAGE, P
VANDEPERRE, P
DABIS, F
MARUM, L
NDUGWA, C
TINDYEBWA, D
ACENG, E
MMIRO, F
机构
[1] BIOCINE CO, EMERYVILLE, CA USA
[2] MD ANDERSON CANC CTR, DEPT EPIDEMIOL, HOUSTON, TX USA
[3] RES TRIANGLE INST, WASHINGTON, DC USA
[4] NCI, VIRAL EPIDEMIOL BRANCH, ROCKVILLE, MD USA
[5] UNIV NEW S WALES, RANDWICK, NSW, AUSTRALIA
[6] HOP ST PIERRE & ERASME, BRUSSELS, BELGIUM
[7] ROYAL FREE HOSP, LONDON NW3 2QG, ENGLAND
[8] GREAT ORMOND ST HOSP SICK CHILDREN, LONDON, ENGLAND
[9] FRAUNKLIN FINKENAU, HAMBURG, GERMANY
[10] COOMBE LYING IN HOSP, DUBLIN 8, IRELAND
[11] UNIV GENOA, HOSP S MARTINO, I-16126 GENOA, ITALY
[12] SAN CAMILLO HOSP, ROME, ITALY
[13] UNIV MILAN, MILAN, ITALY
[14] UNIV PADUA, PADUA, ITALY
[15] CITY HOSP, EDINBURGH, MIDLOTHIAN, SCOTLAND
[16] CATALAN REGISTRY SEROPOSIT CHILDREN, BARCELONA, SPAIN
[17] GEN HOSP, VALENCIA, SPAIN
[18] UNIV HOSP VALENCIA, VALENCIA, SPAIN
[19] KINDERSPITAL ZURICH, CH-8032 ZURICH, SWITZERLAND
[20] LA FE CHILDRENS HOSP, VALENCIA, SPAIN
[21] UNIV HOSP GENEVA, GENEVA, SWITZERLAND
[22] LLANDOUGH HOSP, CARDIFF, S GLAM, WALES
[23] HARVARD UNIV, SCH PUBL HLTH, ORSTOM, CONGO FRANCE, BOSTON, MA 02115 USA
[24] CTR HOSP KIGALI, KIGALI, RWANDA
[25] UGANDA CASE WESTERN RESERVE UNIV COLLABORAT, KAMPALA, UGANDA
[26] PROJET SIDA, KINSHASA, DEM REP CONGO
[27] CTR DIS CONTROL & PREVENT, ATLANTA, GA 30341 USA
[28] ALBERT EINSTEIN COLL MED, BRONX, NY 10467 USA
[29] HOP ST JUSTINE, MONTREAL, PQ H3T 1C5, CANADA
[30] BAY STATE MED CTR, SPRINGFIELD, MA USA
[31] BOSTON CITY HOSP, BOSTON, MA 02118 USA
[32] BRIDGEPORT HOSP, BRIDGEPORT, CT USA
[33] BRONX LEBANON HOSP CTR, DEPT MED, BRONX, NY 10457 USA
[34] CEDARS SINAI LOS ANGELES, LOS ANGELES, CA USA
[35] CHILDRENS HOSP PHILADELPHIA, PHILADELPHIA, PA 19104 USA
[36] CHILDRENS HOSP, BOSTON, MA USA
[37] CHILDRENS HOSP NO CALIF, OAKLAND, CA USA
[38] CHILDRENS HOSP LOS ANGELES, LOS ANGELES, CA 90027 USA
[39] CHILDRENS MED CTR, DALLAS, TX 75235 USA
[40] CHILDRENS MEM HOSP, CHICAGO, IL 60614 USA
[41] CHILDRENS NATL MED CTR, WASHINGTON, DC 20010 USA
[42] COOK FT WORTH CHILDRENS MED CTR, FT WORTH, TX USA
[43] DUKE UNIV, MED CTR, DURHAM, NC USA
[44] HARLEM HOSP MED CTR, NEW YORK, NY USA
[45] HOWARD UNIV HOSP, WASHINGTON, DC USA
[46] JERSEY CITY MED CTR, JERSEY CITY, NJ USA
[47] LINCOLN HOSP CTR, BRONX, NY USA
[48] MONTEFIORE MED CTR, BRONX, NY 10467 USA
[49] NEW YORK MED COLL, NEW YORK, NY USA
[50] N SHORE UNIV HOSP, MANHASSET, NY USA
关键词
D O I
10.1016/S0022-3476(95)70365-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: We evaluated data from prospectively identified twins to understand better the mechanisms and covariates of mother-to-infant transmission of human immunodeficiency virus (HIV). Methods: Using data obtained from an international collaboration and multivariate quasilikelihood modeling, we assessed concordance, birth order, route of delivery, and other factors for HIV infection in 115 prospectively studied twin pairs born to HIV-infected women. Actuarial methods were used to evaluate overall survival and survival free of acquired immunodeficiency syndrome for HIV-infected twins. Results: Infection with HIV occurred in 35% of vaginally delivered firstborn (A) twins, 16% of cesarean-delivered A twins, 15% of vaginally delivered second-born (B) twins, and 8% of cesarean-delivered B twins. In a multivariate model, the adjusted odds ratios for HIV infection were 11.8 (confidence interval: 3.1 to 45.3) for concordance of infection with the co-twin, 2.8 (confidence interval: 1.6 to 5.0) for A versus B twins, and 2.7 (confidence interval: 1.1 to 6.6) for vaginally delivered versus cesarean-delivered twins. Among A twins, 52% (lower confidence limit: 6%) of the transmission risk was related to vaginal delivery, Comparing vaginally delivered A twins (infants most exposed to vaginal mucus and blood) to cesarean-delivered B twins (infants least exposed), 76% (lower confidence limit: 48%) of the transmission risk was related to vaginal exposure. Infected B twins had slightly reduced Quetelet indexes and more rapid development of illnesses related to acquired immunodeficiency syndrome. Conclusions: These results indicate that HIV infection of B twins occurs predominantly in utero, whereas infection of A twins (and, by implication, singletons) occurs predominantly intrapartum, We propose that intrapartum transmission is responsible for the majority of pediatric HIV infections and that reducing exposure to HIV in the birth canal may reduce transmission of the virus from mother to infant.
引用
收藏
页码:625 / 632
页数:8
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