Carolina Lerma-Treviño

Mrs. Carolina Lerma-Treviño

orcid

Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 September 2024 in Environmental Research
Verified
Journal Article
Open access
JFJose Luis Figueroa
Jose Luis Figueroa
ARAlejandra Rodríguez-Atristain
Alejandra Rodríguez-Atristain
LBLuis F. Bautista-Arredondo
Luis F. Bautista-Arredondo
CLCarolina Lerma-Treviño
Carolina Lerma-Treviño
MMMartín Romero Martínez
Martín Romero Martínez
Martha María Téllez-RojoMartha María Téllez-Rojo
Martha María Téllez-Rojo
Lead exposure reduces the cognitive development and future economic prospects of children. While previous studies in high-income settings have explored productivity losses associated with lead exposure, limited research has focused on low and middle-income countries like Mexico. This study aims to provide a comprehensive assessment of the economic implications of lead exposure on Mexican children using, for the first time, nationally representative Blood Lead Levels (BLLs) measurements in children aged 1-4, specifically focusing on the costs of forgone lifetime income due to cognitive losses. BLLs of children aged 1-4 were extracted from the 2018-2019 National Health and Nutrition Survey (ENSANUT). Estimations of cognitive losses were derived from a log-linear relationship between BLLs and IQ loss. Lost lifetime economic productivity per child was calculated, assuming a 2% reduction in lifetime potential productivity for each IQ point lost due to lead exposure, based on previous literature (Attina and Trasande, 2013; Larsen and Sánchez-Triana, 2023). Productivity data were obtained from representative sources for Mexico. The estimated economic loss amounted to US $33.02 billion, equivalent to 2.76% of Mexico's Gross Domestic Product (GDP) in 2019 (calculated for a 1-year cohort). On a national scale, the long-term loss of cognition for children 1-4 years old is 4.14 IQ points per child due to lead exposure, with significant variability across States (range: 3.26 to 5.26). Lead-poisoned children (≥5 μg/dL) suffered an average loss of 6.42 IQ points (range: 0 to 6.97). In terms of economic impact, some States like Chiapas experienced losses of 7.08% of its GDP, while others had losses as low as 0.67%. Intriguingly, states with lower Human Development Index (HDIs) exhibited relatively higher economic losses despite lower average blood lead levels. The heterogeneous impact of lead exposure across Mexican states underscores the necessity for tailored regional policies. These findings emphasize the urgency for targeted interventions and informed policy measures to mitigate the socioeconomic consequences of lead exposure on Mexican children.

13 November 2023 in Salud Pública de México
Verified
Journal Article
Open access
BTBelem Trejo-Valdivia
Belem Trejo-Valdivia
CLCarolina Lerma-Treviño
Carolina Lerma-Treviño
MTMarcela Tamayo-Ortiz
Marcela Tamayo-Ortiz
Alejandra CantoralAlejandra Cantoral
Alejandra Cantoral
JFJosé Luis Figueroa
José Luis Figueroa
Martha María Téllez-RojoMartha María Téllez-Rojo
Martha María Téllez-Rojo
Objetivo. Analizar la asociación entre fuentes de exposición al plomo (FEPb) y la concentración en sangre capilar (PbS) en menores de 1 a 4 años de edad a nivel nacional y regional, así como cuantificar la contribución relativa de las distintas FEPb. Material y métodos. Se utilizaron datos de la Encuesta Nacional de Salud y Nutrición (Ensanut 2022). Las FEPb consideradas fueron uso de loza de barro vidriada con plomo (LBVPb), residencia cercana a sitios contaminados y exposición paraocupacional. Se estimaron prevalencias de intoxicación (PbS ≥ 5.0 mg/dL) y medias geométricas de PbS. Se utilizaron modelos de regresión para PbS (escala logarítmica) y la descomposición Shapley-Owen de R2 para evaluar la contribución relativa de cada FEPb. Resultados. Las FEPb estudiadas explican el 6% de la variabilidad de PbS a nivel nacional; de este, el 87.3% lo explica el uso de LBVPb, el 4.2% otras FEPb ambiental y 1.3% FEPb paraocupacionales. La contribución relativa del uso de LBVPb varía entre regiones, desde 38.1 a 76.8%. Algunas regiones destacan la FEPb ambiental, pero no paraocupacional. Conclusiones. Los resultados confirman que el uso de LBVPb es la principal fuente de exposición reportada y sugieren que la población no identifica las principales FEPb documentadas hasta ahora.

30 June 2024 in Toxics
Verified
Journal Article
Open access
PDF file
CLCarolina Lerma-Treviño
Carolina Lerma-Treviño
LCLeticia Hernandez Cadena
Leticia Hernandez Cadena
JMJorge Octavio Acosta Montes
Jorge Octavio Acosta Montes
GHGeorgina Hernández-Montes
Georgina Hernández-Montes
IAIsabel Alvarado-Cruz
Isabel Alvarado-Cruz
Albino Barraza-VillarrealAlbino Barraza-Villarreal
Albino Barraza-Villarreal
Exposure to arsenic (As) is a public health problem associated with cancer (skin and colon) and it has been reported that epigenetic changes may be a potential mechanism of As carcinogenesis. It is pertinent to evaluate this process in genes that have been associated with cancer, such as ADAMTS9 and C18ORF8. Gestation and delivery data were obtained from the POSGRAD study. Exposure to As was measured in urine during pregnancy. Gene methylation was performed by sodium bisulfite sequencing; 26 CpG sites for the C18ORF8 gene and 21 for ADAMTS9 were analyzed. These sites are located on the CpG islands near the start of transcription. Sociodemographic characteristics were obtained by a questionnaire. The statistical analysis was performed using multiple linear regression models adjusted for potential confounders. Newborns with an As exposure above 49.4 μg g−1 showed a decrease of 0.21% on the methylation rate in the sites CpG15, CpG19, and CpG21 of the C18ORF8 gene (adjusted ß = −0.21, p-value = 0.02). No statistically significant association was found between prenatal exposure to As and methylation of the ADAMTS9 gene. Prenatal exposure to As was associated with decreased DNA methylation at the CpG15, CpG19, and CpG21 sites of the C18ORF8 gene. These sites can provide information to elucidate epigenetic mechanisms associated with prenatal exposure to As and cancer.