Socioeconomic risk markers of congenital Zika syndrome: a nationwide, registry-based study in Brazil

被引:2
|
作者
Paixao, Enny S. [1 ,2 ]
Ferreira Fernandes, Qeren Hapuk R. [2 ]
Cardim, Luciana L. [2 ]
Pescarini, Julia M. [1 ]
Costa, Maria Conceicao N. [3 ]
Falcao, Ila R. [2 ]
Brickley, Elizabeth B. [1 ]
Santos, Andreia Costa [1 ]
Souza, Andre Portela [4 ,5 ]
Carvalho-Sauer, Rita De Cassia Oliveira [6 ]
Smeeth, Liam [7 ]
Rodrigues, Laura C. [1 ]
Barreto, Mauricio L. [2 ]
Teixeira, Maria Gloria [3 ]
机构
[1] London Sch Hyg & Trop Med, Dept Infect Dis Epidemiol, London, England
[2] Fundacao Oswaldo Cruz, Ctr Data & Knowledge Integrat Hlth CIDACS, Goncalo Moniz Inst, Salvador, BA, Brazil
[3] Univ Fed Bahia, Inst Saude Colet, Salvador, BA, Brazil
[4] Getulio Vargas Fdn, Sch Econ, Sao Paulo, Brazil
[5] Getulio Vargas Fdn, Ctr Appl Microecon Studies, Sao Paulo, Brazil
[6] East Reg Hlth Ctr State Hlth Secretariat Bahia, Santo Antonio De Jesus, Brazil
[7] London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London, England
来源
BMJ GLOBAL HEALTH | 2022年 / 7卷 / 09期
基金
英国惠康基金;
关键词
public health; arboviruses; child health; epidemiology; DETERMINANTS; HEALTH; MORTALITY; RACISM; VIRUS;
D O I
10.1136/bmjgh-2022-009600
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
While it is well known that socioeconomic markers are associated with a higher risk of arbovirus infections, research on the relationship between socioeconomic factors and congenital Zika syndrome (CZS) remains limited. This study investigates the relationship between socioeconomic risk markers and live births with CZS in Brazil. We conducted a population-based study using data from all registered live births in Brazil (Live Births Information System) linked with the Public Health Event Record from 1 January 2015 to 31 December 2018. We used logistic regression models to estimate the OR and 95% CIs of CZS based on a three-level framework. In an analysis of 11 366 686 live births, of which 3353 had CZS, we observed that live births of self-identified black or mixed race/brown mothers (1.72 (95% CI 1.47 to 2.01) and 1.37 (95% CI 1.24 to 1.51)) were associated with a higher odds of CZS. Live births from single women compared with married women and those from women with less than 12 years of education compared with those with more than 12 years of education also had higher odds of CZS. In addition, live births following fewer prenatal care appointments had increased odds of CZS in the nationwide data. However, in the analyses conducted in the Northeast region (where the microcephaly epidemic started before the link with Zika virus was established and before preventive measures were known or disseminated), no statistical association was found between the number of prenatal care appointments and the odds of CZS. This study shows that live births of the most socially vulnerable women in Brazil had the greatest odds of CZS. This disproportionate distribution of risk places an even greater burden on already socioeconomically disadvantaged groups, and the lifelong disabilities caused by this syndrome may reinforce existing social and health inequalities.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Hypothyroidism among pediatric cancer patients:: A nationwide, registry-based study
    Madanat, Laura-Maria S.
    Laehteenmaeki, Paeivi M.
    Hurme, Saija
    Dyba, Tadeusz
    Salmi, Toivo T.
    Sankila, Risto
    INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (08) : 1868 - 1872
  • [32] Economic burden of myasthenia gravis in China: a nationwide registry-based study
    Yu, Jiazhou
    Zhang, Huanyu
    Chen, Shanquan
    Dong, Dong
    CURRENT MEDICAL RESEARCH AND OPINION, 2025,
  • [33] Incidence and Outcomes of Acute Respiratory Distress Syndrome A Nationwide Registry-Based Study in Taiwan, 1997 to 2011
    Chen, Wei
    Chen, Yih-Yuan
    Tsai, Ching-Fang
    Chen, Solomon Chih-Cheng
    Lin, Ming-Shian
    Ware, Lorraine B.
    Chen, Chuan-Mu
    MEDICINE, 2015, 94 (43)
  • [34] Incidence and Prevalence of Fibrous Dysplasia/McCune-Albright Syndrome: A Nationwide Registry-Based Study in Denmark
    Meier, Maartje E.
    Vago, Emese
    Abrahamsen, Bo
    Dekkers, Olaf M.
    Horvath-Puho, Erzsebet
    Rejnmark, Lars
    Appelman-Dijkstra, Natasha M.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2024, 109 (06): : 1423 - 1432
  • [35] Holt Oram syndrome: a registry-based study in Europe
    Barisic, Ingeborg
    Boban, Ljubica
    Greenlees, Ruth
    Garne, Ester
    Wellesley, Diana
    Calzolari, Elisa
    Addor, Marie-Claude
    Arriola, Larraitz
    Bergman, Jorieke E. H.
    Braz, Paula
    Budd, Judith L. S.
    Gatt, Miriam
    Haeusler, Martin
    Khoshnood, Babak
    Klungsoyr, Kari
    McDonnell, Bob
    Nelen, Vera
    Pierini, Anna
    Queisser-Wahrendorf, Annette
    Rankin, Judith
    Rissmann, Anke
    Rounding, Catherine
    Tucker, David
    Verellen-Dumoulin, Christine
    Dolk, Helen
    ORPHANET JOURNAL OF RARE DISEASES, 2014, 9 : 156
  • [36] Prevalence and patient characteristics of Mayer-Rokitansky-Kuster-Hauser syndrome: a nationwide registry-based study
    Herlin, Morten
    Bjorn, Anne-Mette Bay
    Rasmussen, Maria
    Trolle, Birgitta
    Petersen, Michael Bjorn
    HUMAN REPRODUCTION, 2016, 31 (10) : 2384 - 2390
  • [37] Prognosis in rheumatoid arthritis patients with COPD: A nationwide, registry-based study
    Hyldgaard, Charlotte
    Lokke, Anders
    Pedersen, Alma Becic
    Ulrichsen, Sinna Pilgaard
    Hilberg, Ole
    Bendstrup, Elisabeth
    Ellingsen, Torkell
    EUROPEAN RESPIRATORY JOURNAL, 2017, 50
  • [38] End-of-life anticancer treatment: A nationwide registry-based study
    Mattsson, Thea O.
    Pottegard, Anton
    Jorgensen, Trine L.
    Green, Anders
    Bliddal, Mette
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2020, 29 : 33 - 33
  • [39] Return to work after stroke: A Swedish nationwide registry-based study
    Westerlind, Emma
    Persson, Hanna C.
    Eriksson, Marie
    Norrving, Bo
    Sunnerhagen, Katharina S.
    ACTA NEUROLOGICA SCANDINAVICA, 2020, 141 (01): : 56 - 64
  • [40] Holt Oram syndrome: a registry-based study in Europe
    Ingeborg Barisic
    Ljubica Boban
    Ruth Greenlees
    Ester Garne
    Diana Wellesley
    Elisa Calzolari
    Marie-Claude Addor
    Larraitz Arriola
    Jorieke EH Bergman
    Paula Braz
    Judith LS Budd
    Miriam Gatt
    Martin Haeusler
    Babak Khoshnood
    Kari Klungsoyr
    Bob McDonnell
    Vera Nelen
    Anna Pierini
    Annette Queisser-Wahrendorf
    Judith Rankin
    Anke Rissmann
    Catherine Rounding
    David Tucker
    Christine Verellen-Dumoulin
    Helen Dolk
    Orphanet Journal of Rare Diseases, 9