Genetic modification of the effect of maternal household air pollution exposure on birth weight in Guatemalan newborns

Reproductive Toxicology

Volumn 50, Issue , 2014, Pages 19-26

  Thompson, Lisa M ^a   Yousefi, Paul ^b   Peñaloza, Reneé ^a   Balmes, John ^b,c   Nina, Holland ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Gene environment interaction; Genetic susceptibility; Glutathione S transferase; Low birth weight; RESPIRE CRECER studies; Woodsmoke

Indexed keywords

GLUTATHIONE TRANSFERASE M1; GLUTATHIONE TRANSFERASE T1; GLUTATHIONE S-TRANSFERASE M1; GLUTATHIONE S-TRANSFERASE T1; GLUTATHIONE TRANSFERASE;

ADULT; ARTICLE; CHIMNEY; COHORT ANALYSIS; CONTROLLED STUDY; COOKING; DNA MODIFICATION; ENVIRONMENTAL EXPOSURE; FEMALE; FIRE; GENE; GENE DELETION; GENE EXPRESSION; GENETIC POLYMORPHISM; GENOTOXICITY; GENOTYPE; GENOTYPE ENVIRONMENT INTERACTION; GSTM1 GENE; GSTT1 GENE; GUATEMALAN; HOUSEHOLD; HUMAN; INDOOR AIR POLLUTION; INFANT; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MOTHER CHILD RELATION; NEWBORN ASSESSMENT; NULL ALLELE; POPULATION GENETICS; PREGNANT WOMAN; RANDOMIZED CONTROLLED TRIAL; SMOKE; ADVERSE EFFECTS; AIR POLLUTION; BIRTH WEIGHT; GENETICS; NEWBORN; PREGNANCY;

AIR POLLUTION; BIRTH WEIGHT; FEMALE; GLUTATHIONE TRANSFERASE; HUMANS; INFANT, NEWBORN; MATERNAL EXPOSURE; PREGNANCY;

EID: 84908295456     PISSN: 08906238     EISSN: 18731708     Source Type: Journal    
DOI: 10.1016/j.reprotox.2014.09.014     Document Type: Article

References (71)

1. Maisonet M., Correa A., Misra D., Jaakkola J.J. A review of the literature on the effects of ambient air pollution on fetal growth. Environ Res 2004, 95:106-115.
2. Sram R.J., Binkova B., Dejmek J., Bobak M. Ambient air pollution and pregnancy outcomes: a review of the literature. Environ Health Perspect 2005, 113:375-382.
3. Glinianaia S.V., Rankin J., Bell R., Pless-Mulloli T., Howel D. Particulate air pollution and fetal health: a systematic review of the epidemiologic evidence. Epidemiology 2004, 15:36-45.
4. UNICEF Low birthweight: Country, regional and global estimates 2004, United Nation's Childrens Fund and World Health Organization, New York.
5. World Health Organization Household energy database: fuel type (rural) 2012.
6. Tielsch J.M., Katz J., Thulasiraj R.D., Coles C.L., Sheeladevi S., Yanik E.L., et al. Exposure to indoor biomass fuel and tobacco smoke and risk of adverse reproductive outcomes, mortality, respiratory morbidity and growth among newborn infants in south India. Int J Epidemiol 2009, 38:1351-1363.
7. Mishra V., Dai X., Smith K.R., Mika L. Maternal exposure to biomass smoke and reduced birth weight in Zimbabwe. Ann Epidemiol 2004, 14:740-747.
8. Boy E., Bruce N., Delgado H. Birth weight and exposure to kitchen wood smoke during pregnancy in rural Guatemala. Environ Health Perspect 2002, 110:109-114.
9. Siddiqui A.R., Gold E.B., Yang X., Lee K., Brown K.H., Bhutta Z.A. Prenatal exposure to wood fuel smoke and low birth weight. Environ Health Perspect 2008, 116:543-549.
10. Thompson L.M., Bruce N., Eskenazi B., Diaz A., Pope D., Smith K.R. Impact of reduced maternal exposures to wood smoke from an introduced chimney stove on newborn birth weight in rural Guatemala. Environ Health Perspect 2011, 119:1489-1494.
11. Pope D.P., Mishra V., Thompson L., Siddiqui A.R., Rehfuess E.A., Weber M., et al. Risk of low birth weight and stillbirth associated with indoor air pollution from solid fuel use in developing countries. Epidemiol Rev 2010, 32:70-81.
12. Bonjour S., Adair-Rohani H., Wolf J., Bruce N.G., Mehta S., Pruss-Ustun A., et al. Solid fuel use for household cooking: country and regional estimates for 1980-2010. Environ Health Perspect 2013, 121:784-790.
13. Delpisheh A., Brabin L., Topping J., Reyad M., Tang A.W., Brabin B.J. A case-control study of CYP1A1, GSTT1 and GSTM1 gene polymorphisms, pregnancy smoking and fetal growth restriction. Eur J Obstet Gynecol Reprod Biol 2009, 143:38-42.
14. Wu F.Y., Wu H.D., Yang H.L., Kuo H.W., Ying J.C., Lin C.J., et al. Associations among genetic susceptibility, DNA damage, and pregnancy outcomes of expectant mothers exposed to environmental tobacco smoke. Sci Total Environ 2007, 386:124-133.
15. Hong Y.C., Lee K.H., Son B.K., Ha E.H., Moon H.S., Ha M. Effects of the GSTM1 and GSTT1 polymorphisms on the relationship between maternal exposure to environmental tobacco smoke and neonatal birth weight. J Occup Environ Med 2003, 45:492-498.
16. Sasaki S., Sata F., Katoh S., Saijo Y., Nakajima S., Washino N., et al. Adverse birth outcomes associated with maternal smoking and polymorphisms in the N-Nitrosamine-metabolizing enzyme genes NQO1 and CYP2E1. Am J Epidemiol 2008, 167:719-726.
17. Wang X., Zuckerman B., Pearson C., Kaufman G., Chen C., Wang G., et al. Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight. JAMA 2002, 287:195-202.
18. Wu T., Hu Y., Chen C., Yang F., Li Z., Fang Z., et al. Passive smoking, metabolic gene polymorphisms, and infant birth weight in a prospective cohort study of Chinese women. Am J Epidemiol 2007, 166:313-322.
19. Aagaard-Tillery K., Spong C.Y., Thom E., Sibai B., Wendel G., Wenstrom K., et al. Pharmacogenomics of maternal tobacco use: metabolic gene polymorphisms and risk of adverse pregnancy outcomes. Obstet Gynecol 2010, 115:568-577.
20. Grazuleviciene R., Danileviciute A., Nadisauskiene R., Vencloviene J. Maternal smoking, GSTM1 and GSTT1 polymorphism and susceptibility to adverse pregnancy outcomes. Int J Environ Res Public Health 2009, 6:1282-1297.
21. Park E.Y., Hong Y.C., Lee K.H., Im M.W., Ha E., Kim Y.J., et al. Maternal exposure to environmental tobacco smoke, GSTM1/T1 polymorphisms and oxidative stress. Reprod Toxicol 2008, 26:197-202.
22. Slama R., Grabsch C., Lepeule J., Siroux V., Cyrys J., Sausenthaler S., et al. Maternal fine particulate matter exposure, polymorphism in xenobiotic-metabolizing genes and offspring birth weight. Reprod Toxicol 2010, 30:600-612.
23. Murdzoska J., Devadason S.G., Khoo S.K., Landau L.I., Young S., Goldblatt J., et al. In utero smoke exposure and role of maternal and infant glutathione s-transferase genes on airway responsiveness and lung function in infancy. Am J Respir Crit Care Med 2010, 181:64-71.
24. Suh Y.J., Kim B.M., Park B.H., Park H., Kim Y.J., Kim H., et al. Cytochrome P450IA1 polymorphisms along with PM(10) exposure contribute to the risk of birth weight reduction. Reprod Toxicol 2007, 24:281-288.
25. Chen D., Hu Y., Yang F., Li Z., Wu B., Fang Z., et al. Cytochrome P450 gene polymorphisms and risk of low birth weight. Genet Epidemiol 2005, 28:368-375.
26. Sata F., Yamada H., Suzuki K., Saijo Y., Yamada T., Minakami H., et al. Functional maternal catechol-O-methyltransferase polymorphism and fetal growth restriction. Pharmacogenet Genom 2006, 16:775-781.
27. Sram R.J., Binkova B., Dejmek J., Chvatalova I., Solansky I., Topinka J. Association of DNA adducts and genotypes with birth weight. Mutat Res 2006, 608:121-128.
28. Naeher L.P., Brauer M., Lipsett M., Zelikoff J.T., Simpson C.D., Koenig J.Q., et al. Woodsmoke health effects: a review. Inhal Toxicol 2007, 19:67-106.
29. Smith K.R. Biofuels, air pollution, and health: a global review 1987, Plenum, New York.
30. Alfaro-Moreno E., Nawrot T.S., Nemmar A., Nemery B. Particulate matter in the environment: pulmonary and cardiovascular effects. Curr Opin Pulm Med 2007, 13:98-106.
31. Pope C.A., Dockery D.W. Health effects of fine particulate air pollution: lines that connect. J Air Waste Manag Assoc 2006, 56:709-742.
32. Chowdhury Z., Edwards R.D., Johnson M., Naumoff Shields K., Allen T., Canuz E., et al. An inexpensive light-scattering particle monitor: field validation. J Environ Monit 2007, 9:1099-1106.
33. World Health Organization WHO air quality guidelines global update 2005 2005, World Health Organization, Bonn, Germany.
34. Saksena S., Thompson L., Smith K.R. Indoor air pollution and exposure database: household measurements in developing countries. V1.1 ed 2003, World Health Organization.
35. Bukowski R., Smith G.C., Malone F.D., Ball R.H., Nyberg D.A., Comstock C.H., et al. Fetal growth in early pregnancy and risk of delivering low birth weight infant: prospective cohort study. BMJ 2007, 334:836.
36. Dary O., Pineda O., Belizan J.M. Carbon monoxide contamination in dwellings in poor rural areas of Guatemala. Bull Environ Contam Toxicol 1981, 26:24-30.
37. Behera D., Dash S., Malik S.K. Blood carboxyhaemoglobin levels following acute exposure to smoke of biomass fuel. Indian J Med Res 1988, 88:522-524.
38. Bruce E.N., Bruce M.C., Erupaka-Chada K. A mathematical modeling approach to risk assessment for normal and anemic women chronically exposed to carbon monoxide from biomass-fueled cookstoves. J. Appl. Physiol. (Bethesda, Md: 1985) 2011, 111:473-484.
39. Viau C., Hakizimana G., Bouchard M. Indoor exposure to polycyclic aromatic hydrocarbons and carbon monoxide in traditional houses in Burundi. Int Arch Occup Environ Health 2000, 73:331-338.
40. Titcombe M.E., Simcik M. Personal and indoor exposure to PM(2).(5) and polycyclic aromatic hydrocarbons in the southern highlands of Tanzania: a pilot-scale study. Environ Monit Assess 2011, 180:461-476.
41. Ansari F.A., Khan A.H., Patel D.K., Siddiqui H., Sharma S., Ashquin M., et al. Indoor exposure to respirable particulate matter and particulate-phase PAHs in rural homes in North India. Environ Monit Assess 2010, 170:491-497.
42. Bonner J.C. Lung fibrotic responses to particle exposure. Toxicol Pathol 2007, 35:148-153.
43. Mossman B.T., Borm P.J., Castranova V., Costa D.L., Donaldson K., Kleeberger S.R. Mechanisms of action of inhaled fibers, particles and nanoparticles in lung and cardiovascular diseases. Part Fibre Toxicol 2007, 4:4.
44. Karttunen V., Myllynen P., Prochazka G., Pelkonen O., Segerback D., Vahakangas K. Placental transfer and DNA binding of benzo(a)pyrene in human placental perfusion. Toxicol Lett 2010, 197:75-81.
45. Topinka J., Milcova A., Libalova H., Novakova Z., Rossner P., Balascak I., et al. Biomarkers of exposure to tobacco smoke and environmental pollutants in mothers and their transplacental transfer to the foetus. Part I: bulky DNA adducts. Mutat Res 2009, 669:13-19.
46. Tang D., Li T.Y., Liu J.J., Chen Y.H., Qu L., Perera F. PAH-DNA adducts in cord blood and fetal and child development in a Chinese cohort. Environ Health Perspect 2006, 114:1297-1300.
47. Perera F.P., Tang D., Rauh V., Lester K., Tsai W.Y., Tu Y.H., et al. Relationships among polycyclic aromatic hydrocarbon-DNA adducts, proximity to the World Trade Center, and effects on fetal growth. Environ Health Perspect 2005, 113:1062-1067.
48. Choi H., Jedrychowski W., Spengler J., Camann D.E., Whyatt R.M., Rauh V., et al. International studies of prenatal exposure to polycyclic aromatic hydrocarbons and fetal growth. Environ Health Perspect 2006, 114:1744-1750.
49. Longo L.D. Carbon monoxide: effects on oxygenation of the fetus in utero. Science 1976, 194:523-525.
50. Garvey D.J., Longo L.D. Chronic low level maternal carbon monoxide exposure and fetal growth and development. Biol Reprod 1978, 19:8-14.
51. Longo L.D., Hill E.P. Carbon monoxide uptake and elimination in fetal and maternal sheep. Am J Physiol 1977, 232:H324-H330.
52. Astrup P., Olsen H.M., Trolle D., Kjeldsen K. Effect of moderate carbon-monoxide exposure on fetal development. Lancet 1972, 2:1220-1222.
53. Moller P., Jacobsen N.R., Folkmann J.K., Danielsen P.H., Mikkelsen L., Hemmingsen J.G., et al. Role of oxidative damage in toxicity of particulates. Free Radic Res 2010, 44:1-46.
54. Valavanidis A., Fiotakis K., Vlachogianni T. Airborne particulate matter and human health: toxicological assessment and importance of size and composition of particles for oxidative damage and carcinogenic mechanisms, Journal of environmental science and health Part C. Environ Carcinogenes Ecotoxicol Rev 2008, 26:339-362.
55. Minelli C., Wei I., Sagoo G., Jarvis D., Shaheen S., Burney P. Interactive effects of antioxidant genes and air pollution on respiratory function and airway disease: a HuGE review. Am J Epidemiol 2011, 173:603-620.
56. Smith K.R., McCracken J.P., Weber M.W., Hubbard A., Jenny A., Thompson L.M., et al. Effect of reduction in household air pollution on childhood pneumonia in Guatemala (RESPIRE): a randomised controlled trial. Lancet 2011, 378:1717-1726.
57. Dix-Cooper L., Eskenazi B., Romero C., Balmes J., Smith K.R. Neurodevelopmental performance among school age children in rural Guatemala is associated with prenatal and postnatal exposure to carbon monoxide, a marker for exposure to woodsmoke. Neurotoxicology 2012, 33:246-254.
58. Smith K.R., McCracken J.P., Thompson L., Edwards R., Shields K.N., Canuz E., et al. Personal child and mother carbon monoxide exposures and kitchen levels: methods and results from a randomized trial of woodfired chimney cookstoves in Guatemala (RESPIRE). J Expo Sci Environ Epidemiol 2010, 20:406-416.
59. Naeher L.P., Smith K.R., Leaderer B.P., Neufeld L., Mage D.T. Carbon monoxide as a tracer for assessing exposures to particulate matter in wood and gas cookstove households of highland Guatemala. Environ Sci Technol 2001, 35:575-581.
60. Northcross A., Chowdhury Z., McCracken J., Canuz E., Smith K.R. Estimating personal PM2.5 exposures using CO measurements in Guatemalan households cooking with wood fuel. J Environ Monit 2010, 12:873-878.
61. Arand M., Muhlbauer R., Hengstler J., Jager E., Fuchs J., Winkler L., et al. A multiplex polymerase chain reaction protocol for the simultaneous analysis of the glutathione S-transferase GSTM1 and GSTT1 polymorphisms. Anal Biochem 1996, 236:184-186.
62. Smith K.R., Bruce N., Arana B. Symposium RESPIRE - the Guatemala stove intervention trial. Epidemiology 2006, 17:S44-S46.
63. Torres M.M., Acosta C.P., Sicard D.M., Groot de Restrepo H. Genetic susceptibility and risk of gastric cancer in a human population of Cauca, Colombia. Biomedica: revista del Instituto Nacional de Salud 2004, 24:153-162.
64. Montero R., Araujo A., Carranza P., Mejia-Loza V., Serrano L., Albores A., et al. Genotype frequencies of polymorphic GSTM1, GSTT1, and cytochrome P450 CYP1A1 in Mexicans. Hum Biol 2007, 79:299-312.
65. Perez-Morales R., Mendez-Ramirez I., Castro-Hernandez C., Martinez-Ramirez O.C., Gonsebatt M.E., Rubio J. Polymorphisms associated with the risk of lung cancer in a healthy Mexican Mestizo population: application of the additive model for cancer. Genet Mol Biol 2011, 34:546-552.
66. Perez-Morales R., Castro-Hernandez C., Gonsebatt M.E., Rubio J. Polymorphism of CYP1A1*2C, GSTM1*0, and GSTT1*0 in a Mexican Mestizo population: a similitude analysis. Hum Biol 2008, 80:457-465.
67. Park L.Y., Muscat J.E., Kaur T., Schantz S.P., Stern J.C., Richie J.P., et al. Comparison of GSTM polymorphisms and risk for oral cancer between African-Americans and Caucasians. Pharmacogenetics 2000, 10:123-131.
68. Hatagima A., Marques C.F., Krieger H., Feitosa M.F. Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) polymorphisms in a Brazilian mixed population. Hum Biol 2004, 76:937-942.
69. Hiragi Cde O., de Oliveira S.F., Hatagima A., Ferreira L.B., Grisolia C.K., Klautau-Guimaraes Mde N. Glutathione S-transferase M1 and T1 polymorphisms in Brazilian African descendants. Hum Biol 2007, 79:131-140.
70. Stachel L., Dean R. Factors contributing to the nutritional status of mothers and young children in rural Guatemala. Maxwell Student Projects, Max-05-2 2006, Environmental Health Sciences, School of Public Health, University of California, Berkeley.
71. Lim S.S., Vos T., Flaxman A.D., Danaei G., Shibuya K., Adair-Rohani H., et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012, 380:2224-2260.