Cesarean Delivery and Hypertension in Early Adulthood

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Citações na Scopus
10
Tipo de produção
article
Data de publicação
2019
Título da Revista
ISSN da Revista
Título do Volume
Editora
OXFORD UNIV PRESS INC
Autores
BARBIERI, Marco Antonio
SILVA, Antonio Augusto Moura da
GOLDANI, Marcelo Zubaran
CARDOSO, Viviane Cunha
STEIN, Aryeh David
BETTIOL, Heloisa
Citação
AMERICAN JOURNAL OF EPIDEMIOLOGY, v.188, n.7, p.1296-1303, 2019
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
The rate of cesarean delivery (CD) is high in many parts of the world. Birth via CD has been associated with adverse later health outcomes, such as obesity, asthma, and type 1 diabetes mellitus. Few studies have focused on hypertension. We investigated the associations of CD with hypertension, systolic blood pressure (BP), and diastolic BP and tested whether body mass index (BMI; weight (kg)/height (m)(2)) was a mediator of these associations in a birth cohort (n = 2,020) assembled in 1978-1979 and followed up in 2002-2004 in Ribeirao Preto, Brazil. The CD rate was 32.0%. Hypertension was present in 11.7% of persons born via CD and 7.7% of those born vaginally. Being born by CD increased the odds of hypertension by 51% (odds ratio = 1.51, 95% confidence interval (CI): 1.10, 2.07). After adjustment for confounders, this estimate changed little (odds ratio = 1.49, 95% CI: 1.07, 2.06). In a mediation analysis, odds ratios for the indirect and direct effects were 1.18 (95% CI: 1.11, 1.25) and 1.31 (95% CI: 0.97, 1.65), respectively. CD also had indirect effects on both systolic and diastolic BP via BMI. Our findings suggest that CD is associated with young-adult hypertension and that this association is at least partially mediated by BMI. This has implications for countries struggling with the burden of noncommunicable diseases and where CD rates are high.
Palavras-chave
cesarean delivery, hypertension, life cycle
Referências
  1. Arnett DK, 2018, CIRC RES, V122, P1409, DOI 10.1161/CIRCRESAHA.118.311342
  2. Bernardi JR, 2015, AM J CLIN NUTR, V102, P295, DOI 10.3945/ajcn.114.105205
  3. Betran AP, 2015, REPROD HEALTH, V12, DOI 10.1186/s12978-015-0043-6
  4. CAMERON N, 1984, ANN HUM BIOL, V11, P261, DOI 10.1080/03014468400007151
  5. Cardoso VC, 2007, BRAZ J MED BIOL RES, V40, P1165, DOI 10.1590/S0100-879X2006005000148
  6. Cardwell CR, 2008, DIABETOLOGIA, V51, P726, DOI 10.1007/s00125-008-0941-z
  7. Clarke Siobhan F, 2012, Gut Microbes, V3, P186, DOI 10.4161/gmic.20168
  8. DAVIES DP, 1972, ARCH DIS CHILD, V47, P938, DOI 10.1136/adc.47.256.938
  9. Emsley R, 2013, PARAMED STATA MODULE
  10. Franklin SS, 1997, CIRCULATION, V96, P308
  11. Franz MB, 2014, EUR J OBSTET GYN R B, V179, P121, DOI 10.1016/j.ejogrb.2014.05.038
  12. Goldani HAS, 2011, AM J CLIN NUTR, V93, P1344, DOI 10.3945/ajcn.110.010033
  13. Goldani MZ, 2013, NUTR J, V12, DOI 10.1186/1475-2891-12-104
  14. Greenland S, 2001, ANNU REV PUBL HEALTH, V22, P189, DOI 10.1146/annurev.publhealth.22.1.189
  15. Haeffner LSB, 2002, ANN HUM BIOL, V29, P627, DOI 10.1080/03014460210145847
  16. Harkanen T, 2014, BMC PUBLIC HEALTH, V14, DOI 10.1186/1471-2458-14-1150
  17. Hense HW, 1995, J HUM HYPERTENS, V9, P935
  18. Horta BL, 2013, PLOS ONE, V8, DOI 10.1371/journal.pone.0074301
  19. Jose PA, 2015, CURR OPIN NEPHROL HY, V24, P403, DOI 10.1097/MNH.0000000000000149
  20. Kajantie E, 2009, STROKE, V40, P1176, DOI 10.1161/STROKEAHA.108.538025
  21. Kuhle S, 2015, OBES REV, V16, P295, DOI 10.1111/obr.12267
  22. Li HT, 2013, INT J OBESITY, V37, P893, DOI 10.1038/ijo.2012.195
  23. Li J, 2017, MICROBIOME, V5, DOI 10.1186/s40168-016-0222-x
  24. Mamun AA, 2013, OBSTET GYNECOL, V122, P1176, DOI 10.1097/AOG.0000000000000016
  25. Mesquita DN, 2013, PLOS ONE, V8, DOI 10.1371/journal.pone.0066827
  26. Molina MC, 2007, BRAZ J MED BIOL RES, V40, P1257, DOI 10.1590/S0100-879X2006005000168
  27. OLSEN J, 1993, SCAND J SOC MED, V21, P90, DOI 10.1177/140349489302100206
  28. Oparil S, 2003, ANN INTERN MED, V139, P761, DOI 10.7326/0003-4819-139-9-200311040-00011
  29. Pardini R, 2001, REV BRASILEIRA CIENC, V9, P45
  30. Pearl J, 2009, CAUSALITY MODELS REA
  31. Pei ZC, 2014, J PEDIATR-US, V164, P1068, DOI 10.1016/j.jpeds.2013.12.044
  32. Reynolds CM, 2014, PHYSIOL REP, V2, DOI 10.14814/phy2.12110
  33. RIBEIRO Adriana Bouças, 2002, Rev. Nutr., V15, P239, DOI 10.1590/S1415-52732002000200012
  34. Schlinzig T, 2009, ACTA PAEDIATR, V98, P1096, DOI 10.1111/j.1651-2227.2009.01371.x
  35. Serapiao-Moraes DF, 2013, EUR J NUTR, V52, P1891, DOI 10.1007/s00394-012-0490-6
  36. Textor J, 2011, EPIDEMIOLOGY, V22, P745, DOI 10.1097/EDE.0b013e318225c2be
  37. Thavagnanam S, 2008, CLIN EXP ALLERGY, V38, P629, DOI 10.1111/j.1365-2222.2007.02780.x
  38. Victora CG, 2011, LANCET, V377, P1863, DOI 10.1016/S0140-6736(11)60138-4
  39. Wald DS, 2009, AM J MED, V122, P290, DOI 10.1016/j.amjmed.2008.09.038
  40. White IR, 2011, STAT MED, V30, P377, DOI 10.1002/sim.4067
  41. Yang T, 2015, HYPERTENSION, V65, P1331, DOI 10.1161/HYPERTENSIONAHA.115.05315