Carlos Martinez-Armenta

Dr. Carlos Martinez-Armenta

orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

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

Representative Publications

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1 August 2022 in Cells
Verified
Journal Article
Open access
PDF file
GJGUADALUPE ELIZABETH JIMÉNEZ-GUTIÉRREZ
GUADALUPE ELIZABETH JIMÉNEZ-GUTIÉRREZ
LMLaura Edith Martínez-Gómez
Laura Edith Martínez-Gómez
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
CPCarlos Pineda
Carlos Pineda
GMGabriela Angelica Martínez-Nava
Gabriela Angelica Martínez-Nava
ALAlberto López-Reyes
Alberto López-Reyes
Sarcopenia is generally an age-related condition that directly impacts the quality of life. It is also related to chronic diseases such as metabolic dysfunction associated with diabetes and obesity. This means that everyone will be vulnerable to sarcopenia at some point in their life. Research to find the precise molecular mechanisms implicated in this condition can increase knowledge for the better prevention, diagnosis, and treatment of sarcopenia. Our work gathered the most recent research regarding inflammation in sarcopenia and new therapeutic agents proposed to target its consequences in pyroptosis and cellular senescence. Finally, we compared dual X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), and ultrasound (US) as imaging techniques to diagnose and follow up on sarcopenia, indicating their respective advantages and disadvantages. Our goal is for the scientific evidence presented here to help guide future research to understand the molecular mechanisms involved in sarcopenia, new treatment strategies, and their translation into clinical practice.

28 August 2023 in Journal of Robotic Surgery
Verified
Journal Article
Closed access
PDF file
CACarlos Suarez Ahedo
Carlos Suarez Ahedo
ALAlberto López-Reyes
Alberto López-Reyes
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
LMLaura E. Martinez-Gomez
Laura E. Martinez-Gomez
GMGabriela Angelica Martínez-Nava
Gabriela Angelica Martínez-Nava
BDBenjamin Domb
Benjamin Domb

16 June 2023 in Journal of Microbiology, Immunology and Infection
Verified
Journal Article
Open access
LMLaura E. Martínez-Gómez
Laura E. Martínez-Gómez
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
DMDaniel Medina-Luna
Daniel Medina-Luna
MOMaría Luisa Ordoñez-Sánchez
María Luisa Ordoñez-Sánchez
TTTeresa Tusié-Luna
Teresa Tusié-Luna
ALAlberto López-Reyes
Alberto López-Reyes
During a viral infection, the immune response is mediated by the toll-like response and myeloid differentiation Factor 88 (MyD88), who play an important role sensing infections such as SARS-CoV-2 who has claimed the lives of more than 6.8 million people around the world. We carried out a cross-sectional with a population of 618 SARS-CoV-2-positive unvaccinated subjects and further classified based on severity: 22% were mild, 34% were severe, 26% were critical, and 18% were deceased. Toll Like Receptor 7 (TLR7) single-nucleotide polymorphisms (rs3853839, rs179008, rs179009, and rs2302267) and MyD88 (rs7744) were genotyped using TaqMan OpenArray. The association of polymorphisms with disease outcomes was performed by logistic regression analysis adjusted by covariates. A significant association of rs3853839 and rs7744 of the TLR7 and MyD88 genes, respectively, was found with COVID-19 severity. The G/G genotype of the rs3853839 TLR7 was associated with the critical outcome showing an Odd Ratio=1.98 (95% IC= 1.04-3.77). The results highlighted an association of the G allele of MyD88 gene with severe, critical and deceased outcomes. Furthermore, in the dominant model (AG+GG vs. AA), we observed an Odd Ratio =1.70 (95% CI = 1.02-2.86) with severe, Odd Ratio = 1.82 (95% CI = 1.04-3.21) with critical, and Odd Ratio =2.44 (95% CI = 1.21-4.9) with deceased outcomes. To our knowledge this work represents an innovator report that highlights the significant association of TLR7 and MyD88 gene polymorphisms with COVID-19 outcomes and the possible implication of the MyD88 variant with D-dimer and IFN-α concentrations.

17 August 2022 in Cells
Verified
Journal Article
Open access
PDF file
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
CACarlos Suarez Ahedo
Carlos Suarez Ahedo
AMAnell Olivos Meza
Anell Olivos Meza
MRMaria del Carmen Camacho Rea
Maria del Carmen Camacho Rea
LMLaura E. Martínez-Gómez
Laura E. Martínez-Gómez
ALAlberto López-Reyes
Alberto López-Reyes
The preservation of the chondrogenic phenotype and hypoxia-related physiological microenvironment are major challenges in the 2D culture of primary human chondrocytes. To address this problem, we develop a 3D culture system generating scaffold-free spheroids from human chondrocytes. Our results highlight the chondrogenic potential of cultured human articular chondrocytes in a 3D system combined with hypoxia independently of the cartilage source. After 14 days of culture, we developed spheroids with homogenous diameter and shape from hyaline cartilage donors. Spheroids generated in hypoxia showed a significantly increased glycosaminoglycans synthesis and up-regulated the expression of SOX9, ACAN, COL2A1, COMP, and SNAI1 compared to those obtained under normoxic conditions. Therefore, we conclude that spheroids developed under hypoxic conditions modulate the expression of chondrogenesis-related genes and native tissue features better than 2D cultures. Thus, this scaffold-free 3D culture system represents a novel in vitro model that can be used for cartilage biology research.

Verified
Journal Article
Open access
PDF file
LRLUCERO A RAMON-LUING
LUCERO A RAMON-LUING
LMLaura Edith Martínez-Gómez
Laura Edith Martínez-Gómez
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
GMGabriela Angelica Martínez-Nava
Gabriela Angelica Martínez-Nava
KMKAREN MEDINA
KAREN MEDINA
Leslie Chavez-GalanLeslie Chavez-Galan
Leslie Chavez-Galan
TNF and IFN-γ are key proinflammatory cytokines implicated in the pathophysiology of COVID-19. Toll-like receptor (TLR)7 and TLR8 are known to recognize SARS-CoV-2 and induce TNF and IFN-γ production. However, it is unclear whether TNF and IFN-γ levels are altered through TLR-dependent pathways and whether these pathways mediate disease severity during COVID-19. This study aimed to investigate the association between TNF/IFN-γ levels and immune cell activation to understand their role in disease severity better. We enrolled 150 COVID-19 patients, who were classified by their systemic TNF and IFN-γ levels (high (H) or normal–low (N-L)) as TNFHIFNγH, TNFHIFNγN-L, TNFN-LIFNγH, and TNFN-LIFNγN-L. Compared to patients with TNFN-LIFNγN-L, patients with TNFHIFNγH had high systemic levels of pro- and anti-inflammatory cytokines and cytotoxic molecules, and their T cells and monocytes expressed TNF receptor 1 (TNFR1). Patients with TNFHIFNγH presented the SNP rs3853839 to TLR7 and increased levels of MYD88, NFκB, and IRF7 (TLR signaling), FADD, and TRADD (TNFR1 signaling). Moreover, critical patients were observed in the four COVID-19 groups, but patients with TNFHIFNγH or TNFHIFNγN-L most required invasive mechanical ventilation. We concluded that increased TNF/IFN-γ levels are associated with hyperactive immune cells, whereas normal/low levels are associated with hypoactivity, suggesting a model to explain that the pathophysiology of critical COVID-19 may be mediated through different pathways depending on TNF and IFN-γ levels. These findings highlight the potential for exploring the modulation of TNF and IFN-γ as a therapeutic strategy in severe COVID-19.

1 October 2025 in JBJS Open Access
Verified
Journal Article
Open access
CACarlos Suarez Ahedo
Carlos Suarez Ahedo
MQMiguel Alejandro Quintero-Quintero
Miguel Alejandro Quintero-Quintero
CMCarlos Martinez-Armenta
Carlos Martinez-Armenta
LMLaura E. Martínez-Gómez
Laura E. Martínez-Gómez
GMGabriela A. Martínez-Nava
Gabriela A. Martínez-Nava
ALAlberto López-Reyes
Alberto López-Reyes
» Dual mobility cup (DMC) implants reduce dislocation rates in both primary and revision total hip arthroplasty (THA), particularly in high-risk patients with neuromuscular disorders, cognitive impairment, or obesity. » The dual articulation mechanism enhances joint stability by increasing jump distance and the head-to-neck ratio, without compromising range of motion. » Incorporation of highly cross-linked polyethylene and vitamin E–infused liners improves wear resistance, supporting broader use in younger, more active patients. » Long-term survivorship of modern DMCs is comparable or superior to fixed-bearing implants, with a lower revision burden and durable fixation when appropriately selected and implanted. » Systemic metal ion levels remain low in well-functioning modular DMCs, though continued monitoring is recommended in younger patients and those with reproductive potential.