Arnulfo Hernán Nava-Zavala
Mexican Social Security Institute
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Featured researches published by Arnulfo Hernán Nava-Zavala.
Rheumatic Diseases Clinics of North America | 2009
Ignacio García-De La Torre; Arnulfo Hernán Nava-Zavala
Acute bacterial arthritis usually is caused by gonococcal or nongonococcal infection of the joints. Nongonococcal and gonococcal arthritis are the most potentially dangerous and destructive forms of acute arthritis. These bacterial infections of the joints are usually curable with treatment, but morbidity and mortality are still significant in patients who have underlying rheumatoid arthritis, patients who have prosthetic joints, elderly patients, and patients who have severe and multiple comorbidities. This article reviews the risk factors, pathogenesis, clinical manifestations, diagnosis, and treatment of nongonococcal and gonococcal arthritis.
Clinical & Developmental Immunology | 2015
Alberto Daniel Rocha-Muñoz; Jorge I. Gamez-Nava; Eva Maria Olivas-Flores; Mayra Mejía; Pablo Juárez-Contreras; Erika Aurora Martínez-García; Esther Guadalupe Corona-Sanchez; Tania Marlen Rodríguez-Hernández; Mónica Vázquez-Del Mercado; Mario Salazar-Páramo; Arnulfo Hernán Nava-Zavala; Ernesto Germán Cardona-Muñoz; Alfredo Celis; Laura Gonzalez-Lopez
Objective. To evaluate whether serum titers of second-generation anticyclic citrullinated peptide antibodies (anti-CCP2) are associated with the severity and extent of interstitial lung disease in rheumatoid arthritis (RA-ILD). Methods. In across-sectional study, 39 RA-ILD patients confirmed by high-resolution computed tomography (HRCT) were compared with 42 RA without lung involvement (RA only). Characteristics related to RA-ILD were assessed in all of the patients and serum anti-CCP2 titers quantified. Results. Higher anti-CCP2 titers were found in RA-ILD compared with RA only (medians 77.9 versus 30.2 U/mL, P < 0.001). In the logistic regression analysis after adjustment for age, disease duration (DD), smoke exposure, disease activity, functioning, erythrocyte sedimentation rate, and methotrexate (MTX) treatment duration, the characteristics associated with RA-ILD were higher anti-CCP2 titers (P = 0.003) and + RF (P = 0.002). In multivariate linear regression, the variables associated with severity of ground-glass score were anti-CCP2 titers (P = 0.02) and with fibrosis score DD (P = 0.01), anti-CCP2 titers (P < 0.001), and MTX treatment duration (P < 0.001). Conclusions. Anti-CCP2 antibodies are markers of severity and extent of RA-ILD in HRCT. Further longitudinal studies are required to identify if higher anti-CCP2 titers are associated with worst prognosis in RA-ILD.
Clinical & Developmental Immunology | 2015
María Guadalupe Zavala-Cerna; Maria Cristina Moran-Moguel; Jesus Alejandro Cornejo-Toledo; Norma Guadalupe Gonzalez-Montoya; José Sánchez-Corona; Mario Salazar-Páramo; Arnulfo Hernán Nava-Zavala; Erika Anita Aguilar-Chavez; Miriam Fabiola Alcaraz-Lopez; Alicia Guadalupe González-Sánchez; Laura Gonzalez-Lopez; Jorge I. Gamez-Nava
Bone disease in rheumatoid arthritis (RA) is a complex phenomenon where genetic risk factors have been partially evaluated. The system formed by receptor activator for nuclear factor-κB (RANK), receptor activator for nuclear factor-κB ligand (RANKL), and osteoprotegerin (OPG): RANK/RANKL/OPG is a crucial molecular pathway for coupling between osteoblasts and osteoclasts, since OPG is able to inhibit osteoclast differentiation and activation. We aim to evaluate the association between SNPs C950T (rs2073617), C209T (rs3134069), T245G (rs3134070) in the TNFRSF11B (OPG) gene, and osteoporosis in RA. We included 81 women with RA and 52 healthy subjects in a cross-sectional study, genotyped them, and measured bone mineral density (BMD) at the lumbar spine and the femoral neck. Mean age in RA was 50 ± 12 with disease duration of 12 ± 8 years. According to BMD results, 23 (33.3%) were normal and 46 (66.7%) had osteopenia/osteoporosis. We found a higher prevalence of C allele for C950T SNP in RA. Polymorphisms C209T and T245G did not reach statistical significance in allele distribution. Further studies including patients from other regions of Latin America with a multicenter design to increase the sample size are required to confirm our findings and elucidate if C950T SNP could be associated with osteoporosis in RA.
Journal of International Medical Research | 2017
Laura Gonzalez-Lopez; Nicte Selene Fajardo-Robledo; A. Miriam Saldaña-Cruz; Inocente V. Moreno-Sandoval; David Bonilla-Lara; Soraya Amali Zavaleta-Muñiz; Arnulfo Hernán Nava-Zavala; Paulina Hernández-Cuervo; Alberto Daniel Rocha-Muñoz; Norma Alejandra Rodriguez-Jimenez; María Luisa Vázquez-Villegas; J. Francisco Muñoz-Valle; Mario Salazar-Páramo; Ernesto Germán Cardona-Muñoz; Jorge I. Gamez-Nava
Objective To identify correlations of the serum leptin, adiponectin, interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) concentrations with the clinical characteristics, presence of spinal syndesmophytes, and body composition in patients with ankylosing spondylitis (AS). Methods Forty-eight patients with AS were compared with 41 sex- and age-matched controls. Assessment included clinical characteristics and the presence of spinal syndesmophytes. The serum leptin, adiponectin, TNF-α, and IL-6 concentrations were determined. Body composition was evaluated using dual-energy X-ray absorptiometry. Results Patients with AS and controls had similar fat mass and lean mass. Patients with AS had higher serum TNF-α and leptin concentrations than controls (52.3 vs. 1.5 pg/mL and 17.2 vs. 9.0 µg/mL, respectively). The IL-6 and adiponectin concentrations were not significantly different between the two groups. Patients with syndesmophytes had higher leptin concentrations than those without syndesmophytes (22.1 vs. 10.9 µg/mL); this difference remained after adjustment for the body mass index. Conclusion Elevated leptin concentrations are associated with spinal radiographic damage in patients with AS and can serve as a biomarker. Future studies should evaluate whether leptin might be a potential target for treatments to avoid structural damage.
Archivos De Bronconeumologia | 2015
Laura Gonzalez-Lopez; Alberto D. Rocha-Muñoz; Eva Maria Olivas-Flores; Araceli Garcia-Gonzalez; Ana R. Peguero-Gómez; Juan Flores-Navarro; Alberto I. Villa-Manzano; Soraya Amali Zavaleta-Muñiz; Mario Salazar-Páramo; Mayra Mejía; Pablo Juárez-Contreras; Mónica Vázquez-Del Mercado; Ernesto Germán Cardona-Muñoz; Benjamín Trujillo-Hernández; Arnulfo Hernán Nava-Zavala; Jorge I. Gamez-Nava
BACKGROUND Interstitial lung disease (ILD) is a frequent complication in progressive systemic sclerosis (SSc), being present in 25% to 90% of cases. OBJECTIVES To evaluate whether serum levels of procollagen typei and iii aminoterminal propeptide (PINP and PIIINP) correlate with severity and patterns of ILD in Mexican women with SSc. METHODS Thirty three SSc patients were assessed for disease characteristics and anti-topoisomerase antibodies (topoi), and also underwent pulmonary function tests and high-resolution computed tomography (HRCT). Nineteen patients had ILD+SSc, and 14 had no lung involvement (no ILD-SSc); data were compared with those from 45 healthy controls. PINP and PIIINP were assessed in all 3 groups. RESULTS Patients with SSc had higher PINP and PIIINP vs controls (P=.001, P<.001, respectively). Compared to no ILD-SSc patients, those with ILD+SSc had longer disease duration in years (P=.005), higher modified Rodnan skin score (P<.001), higher Health Assessment Questionnaire-Disability-Index scores (P<.001), higher topoi U/mL (P<.001), PINP (49.28±28.63 vs. 32.12±18.58μg/L, P=.05), and PIIINP (4.33±1.03 vs. 2.67±1.26μg/L, P<.001) levels. ILD severity based on total HRCT correlated with PINP (r=.388, P=.03) and PIIINP (P=.594, P<.001). On adjusted analysis, ILD severity was associated with disease duration (P=.037), PIIINP (P=.038), and topoi (P=.045). CONCLUSIONS PINP and PIIINP are useful markers for severe ILD+SSc, suggesting they could play a role in the follow-up of this complication in SSc.
Archive | 2018
Benjamín Rubio-Jurado; L Balderas-Peña; Eduardo E. García-Luna; María Guadalupe Zavala-Cerna; Carlos Riebeling-Navarro; Pedro A Reyes; Arnulfo Hernán Nava-Zavala
Neoplasms exhibits a high incidence and mortality rates due to their complex and commonly overlapping clinical, biochemical, and morphologic profiles influenced by acquired or inherited molecular abnormalities, cell of origin, and level of differentiation. Obesity appears related to ~20% of cancers including endometrial, esophageal, colorectal, postmenopausal breast, prostate, and renal. Several factors other than obesity, i.e., insulin, insulin-like growth factor, sexual hormones, and adipokines may play a potential role in neoplasia. Cancer-associated hypercoagulable and thrombotic states are influenced by abnormalities in the vascular wall and susceptibility to invasion, interference in blood flow and increase in circulating tissue factor and thrombin, activation of cell growth factors, the presence of a central catheter, chemotherapies, neoplasm type, and surgery. In cancer, thromboembolic complications are the second most frequent cause of death with pulmonary thromboembolism in ~50% of cases postmortem. Thrombosis worsens prognosis as demonstrated with a survival rate as low as 12% per year vs 36% in nonthrombic patients. Deep vein thrombosis is the most frequent thromboembolic complication in cancer. It is usually detected at diagnosis and within the first 3 months of chemotherapy. The underlining mechanisms of this association should be further studied to identify patients at higher risk and develop adequate prevention, diagnostic, and treatment measures. The D-dimer test can be successfully used to assess the fibrinolytic phase of coagulation and as such is routinely used in suspected cases of deep vein thrombosis and pulmonary thromboembolism. In addition, significant advances have been made in understanding the composition and functional capabilities of the gut microbiota in the inflammatory process, obesity, and its roles in cancer; however, the intricate balance that exists within the microbiota may not only affect the host directly, it can also disrupt the entire microbial community. CONCLUSIONS Cancer is a prothrombotic and inflammatory state in which the activation of coagulation is related to tumor growth, angiogenesis, and metastasis. It is important to identify the relationship between body mass index with these processes and clarify their importance in cancer prognosis. Future research should answer the question if manipulation of resident microbial communities could potentially improve prognosis and treatment outcome.
Gaceta Mexicana de Oncolog�a | 2017
Samuel Agredano-Pérez; Ignacio Mariscal-Ramírez; Carlos Ronquillo-Carreón; Tomas Pineda-Razo; Arnulfo Hernán Nava-Zavala
Worldwide, colorectal cancer is the third cause of death in men and the second leading cause of death in women, with about 1.2 million new cases diagnosed and 600,000 estimated deaths. A significant proportion of patients are diagnosed with metastatic disease at diagnosis. Angiogenesis is the formation of new blood vessels from existing ones, which play an important role in tumor growth and progression. Factors related to endothelial growth, including vascular endothelial growth factor, have been identified. Several studies have shown the PALABRAS CLAVE Angiogénesis; Cáncer colorrectal; Estado protrombótico; Pronóstico; Trombosis; Factor de crecimiento endotelial vascular (VEGF)
Case reports in infectious diseases | 2017
Stefania Petarra-del Rio; Adrian Rodriguez-Hernandez; Luis Anguiano-Landa; Georgina Aguilar-Portillo; Isidro Zavala-Trujillo; Arnulfo Hernán Nava-Zavala; María Guadalupe Zavala-Cerna
Background Cytomegalovirus (CMV) pulmonary involvement is rarely associated with IRIS; therefore, limited information is available. Case Presentation Here, we describe the case of a 43-year-old HIV-infected male who developed an unusual case of IRIS after cytomegalovirus (CMV) pneumonia. Clinically there was a progressive and paradoxical worsening of respiratory distress, despite being treated for CMV after initiation with antiretroviral therapy. Chest X-ray revealed disseminated infiltrates in both lungs; chest CT-scan showed generalized lung involvement and mediastinal adenopathy. Pulmonary biopsy confirmed CMV pneumonia with the observation of typical viral inclusions on pneumocytes. Conclusions CMV pneumonia can be associated with the development of IRIS requiring treatment with immunosuppressants and immunomodulatory drugs.
Clinical Lymphoma, Myeloma & Leukemia | 2015
Benjamín Rubio-Jurado; Alejandra Tello-González; Lili Bustamante-Chávez; Aurora de la Peña; Carlos Riebeling-Navarro; Arnulfo Hernán Nava-Zavala
BACKGROUND Patients with cancer exhibit changes in their hemostatic mechanisms. The D-dimer (D-D) is the most important subproduct of fibrinolysis, and urokinase plasminogen activator receptor (uPAR) is related to invasiveness and metastases, and is overexpressed in neoplastic cells. The objective of this study was to identify in patients with hematological neoplasia, the serum levels of uPAR and D-D, and to determine their effects on outcome. PATIENTS AND METHODS A cross-sectional study was performed. Clinical and demographic data were obtained from the clinical chart. Determination of uPAR in serum (pg/L) was performed using an enzyme-linked immunosorbent assay, and D-D (μg/dL) using nephelometry. RESULTS We included 42 patients (35 with lymphomas). Statistically significant differences were found in D-D (P < .001) and uPAR (P < .01) between patients and control participants. Response was an accumulated clinical outcome. We observed statistical differences between groups (P < .001). D-D was positive in 70% of cases. CONCLUSION We found differences in D-D serum levels and soluble uPAR between control participants and patients with lymphoma. These results indicate that D-D serum levels and soluble uPAR should be considered biomarkers of response and survival in patients with lymphoma.
Clinical & Developmental Immunology | 2015
Alberto Daniel Rocha-Muñoz; Aniel Jessica Leticia Brambila-Tapia; María Guadalupe Zavala-Cerna; José Clemente Vásquez-Jiménez; Liliana Faviola De la Cerda-Trujillo; Mónica Vázquez-Del Mercado; Norma Alejandra Rodriguez-Jimenez; Valeria Diaz-Rizo; Viviana Díaz-González; Ernesto Germán Cardona-Muñoz; Ingrid Patricia Dávalos-Rodríguez; Mario Salazar-Páramo; Jorge I. Gamez-Nava; Arnulfo Hernán Nava-Zavala; Laura Gonzalez-Lopez
Objective. To evaluate the effect of anti-TNF agents plus synthetic disease modifying antirheumatic drugs (DMARDs) versus DMARDs alone for ankylosing spondylitis (AS) with reduced pulmonary function vital capacity (FVC%). Methods. In an observational study, we included AS who had FVC% <80% at baseline. Twenty patients were taking DMARDs and 16 received anti-TNF + DMARDs. Outcome measures: changes in FVC%, BASDAI, BASFI, 6-minute walk test (6MWT), Borg scale after 6MWT, and St. Georges Respiratory Questionnaire at 24 months. Results. Both DMARDs and anti-TNF + DMARDs groups had similar baseline values in FVC%. Significant improvement was achieved with anti-TNF + DMARDs in FVC%, at 24 months, when compared to DMARDs alone (P = 0.04). Similarly, patients in anti-TNF + DMARDs group had greater improvement in BASDAI, BASFI, Borg scale, and 6MWT when compared to DMARDs alone. After 2 years of follow-up, 14/16 (87.5%) in the anti-TNF + DMARDs group achieved the primary outcome: FVC% ≥80%, compared with 11/20 (55%) in the DMARDs group (P = 0.04). Conclusions. Patients with anti-TNF + DMARDs had a greater improvement in FVC% and cardiopulmonary scales at 24 months compared with DMARDs. This preliminary study supports the fact that anti-TNF agents may offer additional benefits compared to DMARDs in patients with AS who have reduced FVC%.