Erik Lizárrga-Verdugo

Dr. Erik Lizárrga-Verdugo


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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Carlos Ernesto Mora-PalazuelosCarlos Ernesto Mora-Palazuelos
Carlos Ernesto Mora-Palazuelos
CVCarlos Esteban Villegas-Mercado
Carlos Esteban Villegas-Mercado
MAMariana Melisa Avendaño-Félix
Mariana Melisa Avendaño-Félix
ELErik Lizárrga-Verdugo
Erik Lizárrga-Verdugo
JRJosé Geovanni Romero-Quintana
José Geovanni Romero-Quintana
MBMercedes Bermúdez
Mercedes Bermúdez
The main complications causing practically 75% of all maternal deaths are severe bleeding, infections, and high blood pressure during pregnancy (preeclampsia (PE) and eclampsia). The usefulness of ncRNAs as clinical biomarkers has been explored in an extensive range of human diseases including pregnancy-related diseases such as PE. Immunological dysregulation show that the Th1/17:Th2/Treg ratio is “central and causal” to PE. However, there is evidence of the involvement of placenta-expressed miRNAs and lncRNAs in the immunological regulation of crucial processes of placenta development and function during pregnancy. Abnormal expression of these molecules is related to immune physiopathological processes that occur in PE. Therefore, this work aims to describe the importance of miRNAs and lncRNAs in immune dysregulation in PE. Interestingly, multiple ncRNAS are involved in the immune dysregulation of PE participating in type 1 immune response regulation, immune microenvironment regulation in placenta promoting inflammatory factors, trophoblast cell invasion in women with Early-Onset PE (EOPE), placental development, and angiogenesis, promotion of population of M1 and M2, proliferation, invasion, and migration of placental trophoblast cells, and promotion of invasion and autophagy through vias such as PI3K/AKT/mTOR, VEGF/VEGFR1, and TLR9/STAT3.

Verified
Journal Article
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ELErik Lizárrga-Verdugo
Erik Lizárrga-Verdugo
SBSaúl Armando Beltrán
Saúl Armando Beltrán
Erick Paul Gutiérrez-GrijalvaErick Paul Gutiérrez-Grijalva
Erick Paul Gutiérrez-Grijalva
MMMarisol Montoya Moreno
Marisol Montoya Moreno
PGPerla Yareli Gutiérrez-Arzapalo
Perla Yareli Gutiérrez-Arzapalo
Carlos Ernesto Mora-PalazuelosCarlos Ernesto Mora-Palazuelos
Carlos Ernesto Mora-Palazuelos
Placenta accreta spectrum (PAS) disorders are characterized by abnormal trophoblastic invasion into the myometrium, leading to significant maternal health risks. PAS includes placenta accreta (invasion < 50% of the myometrium), increta (invasion > 50%), and percreta (invasion through the entire myometrium). The condition is most associated with previous cesarean deliveries and increases in chance with the number of prior cesarians. The increasing global cesarean rates heighten the importance of early PAS diagnosis and management. This review explores genetic expression and key regulatory processes, such as apoptosis, cell proliferation, invasion, and inflammation, focusing on signaling pathways, genetic expression, biomarkers, and non-coding RNAs involved in trophoblastic invasion. It compiles the recent scientific literature (2014–2024) from the Scopus, PubMed, Google Scholar, and Web of Science databases. Identifying new biomarkers like AFP, sFlt-1, β-hCG, PlGF, and PAPP-A aids in early detection and management. Understanding genetic expression and non-coding RNAs is crucial for unraveling PAS complexities. In addition, aberrant signaling pathways like Notch, PI3K/Akt, STAT3, and TGF-β offer potential therapeutic targets to modulate trophoblastic invasion. This review underscores the need for interdisciplinary care, early diagnosis, and ongoing research into PAS biomarkers and molecular mechanisms to improve prognosis and quality of life for affected women.

11 July 2023 in The Lancet Regional Health - Americas
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Journal Article
Open access
SMSofia E. Madueña-Angulo
Sofia E. Madueña-Angulo
SBSaúl Armando Beltrán
Saúl Armando Beltrán
ELEmir Leal-Leon
Emir Leal-Leon
JCJose A. Contreras-Gutierrez
Jose A. Contreras-Gutierrez
ELErik Lizárrga-Verdugo
Erik Lizárrga-Verdugo
Daniel DiazDaniel Diaz
Daniel Diaz
Reliable national estimations for blindness and vision impairment are fundamental to assessing their burden and developing public health policies. However, no comprehensive analysis is available for Mexico. Therefore, in this observational study we describe the national burden of blindness and vision loss by cause and severity during 2019. Using public data from the Global Burden of Disease (GBD) study 2019, we present national prevalence and years lived with disability (YLDs) counts and crude and age-standardized rates (per 100,000 people) of total, severity- and cause-specific blindness and vision impairment with 95% uncertainty intervals (UIs) by sex and age group. In Mexico, the burden of blindness and vision impairment was estimated at 11.01 million (95% UI, 9.25–13.11) prevalent cases and 384.96 thousand (259.57–544.24) YLDs during 2019. Uncorrected presbyopia caused the highest burden (6.06 million cases, 4.36–8.08), whereas severe vision loss and blindness affected 619.40 thousand (539.40–717.73) and 513.84 thousand (450.59–570.98) people, respectively. Near vision loss and refraction disorders caused 78.7% of the cases, whereas neonatal disorders and age-related macular degeneration were among the least frequent. Refraction disorders were the main cause of moderate and severe vision loss (61.44 and 35.43%), and cataracts were the second most frequent cause of blindness (26.73%). Females suffered an overall higher burden of blindness and vision impairment (54.99% and 52.85% of the total cases and YLDs), and people >50 years of age suffered the highest burden, with people between 70 and 74 years being the most affected. Vision loss represents a public health problem in Mexico, with women and older people being the most affected. Although the causes of vision loss contribute differentially to the severity of visual impairment, most of the impairment is avoidable. Consequently, a concerted effort at different levels is needed to alleviate this burden. This study received no funding.

28 December 2023 in Cancers
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SBSaúl Armando Beltrán
Saúl Armando Beltrán
JCJose A. Contreras-Gutierrez
Jose A. Contreras-Gutierrez
ELErik Lizárrga-Verdugo
Erik Lizárrga-Verdugo
Erick Paul Gutiérrez-GrijalvaErick Paul Gutiérrez-Grijalva
Erick Paul Gutiérrez-Grijalva
KLKenia Lopez-Lopez
Kenia Lopez-Lopez
Daniel DiazDaniel Diaz
Daniel Diaz
The global burden of cancer is on the rise, with varying national patterns. To gain a better understanding and control of cancer, it is essential to provide national estimates. Therefore, we present a comparative description of cancer incidence and mortality rates in Mexico from 1990 to 2019, by age and sex for 29 different cancer groups. Based on public data from the Global Burden of Disease Study 2019, we evaluated the national burden of cancer by analyzing counts and crude and age-standardized rates per 100,000 people with 95% uncertainty intervals for 2019 and trends using the annual percentage change from 1990 to 2019. In 2019, cancer resulted in 222,060 incident cases and 105,591 deaths. In 2019, the highest incidence of cancer was observed in non-melanoma skin cancer, prostate cancer, and breast cancer. Additionally, 53% of deaths were attributed to six cancer groups (lung, colorectal, stomach, prostate, breast, and pancreatic). From 1990 to 2019, there was an increasing trend in incidence and mortality rates, which varied by 10–436% among cancer groups. Furthermore, there were cancer-specific sex differences in crude and age-standardized rates. The results show an increase in the national cancer burden with sex-specific patterns of change. These findings can guide national efforts to reduce health loss due to cancer.

9 June 2025 in Phytochemistry Reviews
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MPManuel A. Picos-Salas
Manuel A. Picos-Salas
Luis Angel Cabanillas BojórquezLuis Angel Cabanillas Bojórquez
Luis Angel Cabanillas Bojórquez
Nayely Leyva-LópezNayely Leyva-López
Nayely Leyva-López
CECristina Alicia Elizalde-Romero
Cristina Alicia Elizalde-Romero
MMManuel de Jesús Bernal Millán
Manuel de Jesús Bernal Millán
Erick Paul Gutiérrez-GrijalvaErick Paul Gutiérrez-Grijalva
Erick Paul Gutiérrez-Grijalva