Ernesto Sosa

ORCID: 0000-0002-3459-923X
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About
Contact & Profiles
Research Areas
  • Pituitary Gland Disorders and Treatments
  • Growth Hormone and Insulin-like Growth Factors
  • Adrenal and Paraganglionic Tumors
  • Ophthalmology and Eye Disorders
  • Glioma Diagnosis and Treatment
  • Cancer, Hypoxia, and Metabolism
  • Adrenal Hormones and Disorders
  • TGF-β signaling in diseases
  • Hormonal Regulation and Hypertension
  • Spanish Literature and Culture Studies
  • Neuroblastoma Research and Treatments
  • Philosophical Thought and Analysis
  • Bariatric Surgery and Outcomes
  • Galician and Iberian cultural studies
  • Social Sciences and Policies
  • Political Dynamics in Latin America
  • Classical Philosophy and Thought
  • Myasthenia Gravis and Thymoma
  • Thyroid Disorders and Treatments
  • Diet and metabolism studies
  • Neuroendocrine Tumor Research Advances
  • Thyroid Cancer Diagnosis and Treatment
  • Respiratory Support and Mechanisms
  • History of Education in Spain
  • Comparative Literary Analysis and Criticism

Centro Medico Nacional Siglo XXI
2015-2025

Mexican Social Security Institute
2015-2025

Hospital de Especialidades
2015-2025

Red de Investigación Cardiovascular
2023

Sociedad Española de Endocrinología y Nutrición
2023

Communauté urbaine de Lyon
2018

Hôpital de la Croix-Rousse
2011-2017

Hospices Civils de Lyon
2017

Université Claude Bernard Lyon 1
2017

Institute of Experimental Endocrinology of the Slovak Academy of Sciences
2009

Acromegaly is usually due to the excessive secretion of GH by a pituitary adenoma. It frequently accompanied comorbidities that compromise quality life and results in elevated mortality rates.To evaluate morbidity patients with acromegaly receiving multimodal care.Tertiary care center.Retrospective evaluation 442 (65.4% women; mean age, 43.5 ± 13.1 y) followed for median 6 years (interquartile range [IQR], 3-10).Twenty-two died during study period (4.9%), representing total standardized...

10.1210/jc.2014-2670 article EN The Journal of Clinical Endocrinology & Metabolism 2014-12-01

Currently, bariatric surgery is the most effective treatment for severe obesity and its metabolic complications; however, 15-35% of patients that undergo do not reach their goal weight loss. The aim this study was to determine proportion didn't an excess loss 50% or more during first 12 months factors associated failure.We obtained demographic, anthropometric biochemical information from 130 with who underwent in our institution between 2012 2017. We used self-reports physical activity,...

10.1186/s12902-020-0499-4 article EN cc-by BMC Endocrine Disorders 2020-02-05

Pituitary adenomas (PA) are the second most common intracranial tumors. These neoplasms classified according to hormone they produce. The majority of PA occur sporadically, and their molecular pathogenesis is incompletely understood. present transcriptomic methylomic analysis revealed that segregate into three clusters transcription factor driving terminal differentiation. First cluster, driven by NR5A1, consists clinically non-functioning (CNFPA), comprising gonadotrophinomas null cell;...

10.1038/s41598-020-76555-8 article EN cc-by Scientific Reports 2020-11-09

Genetic tests are part of the routine clinical approach to syndromic and nonsyndromic phenotypes neuroendocrine neoplasms (NENs). Current data on phenotype-genotype associations in NENs, however, do not accurately represent all populations. To describe frequency, inventory, germline defects associated with multiple types NENs a Mexican cohort. Blood DNA from adults was analyzed 53-gene NGS panel developed ad hoc (n=90) or Sanger sequencing (n=2). Single nucleotide variants, indels structural...

10.1210/clinem/dgaf075 article EN cc-by-nc-nd The Journal of Clinical Endocrinology & Metabolism 2025-02-04

Background: Cardiomyopathy is the leading cause of morbidity and mortality in patients with acromegaly. Pharmacological surgical treatment disease has been associated morphological functional benefits for heart, but other studies have shown that condition its effects may be irreversible. This study aims to uncover most frequent echocardiographic changes cardiomyopathy due Methods: An observational, descriptive, cross-sectional was performed. Patients were referred from Endocrinology...

10.3390/biomedicines13030605 article EN cc-by Biomedicines 2025-03-01

Familial partial lipodystrophy type 2 is a rare disease, particularly when it caused by nonclassical gene variants. A high index of suspicion essential for timely diagnosis. We present the case 32-year-old woman, referred to evaluation possible Cushing syndrome, which was clinically and biochemically ruled out. Yet, due finding rather abnormal fat distribution during physical examination, diagnosis cogitated. Whole-exome sequencing revealed missense variant exon 11 R582H encoding Laminin...

10.20945/2359-4292-2024-0293 article EN PubMed 2025-03-24

Background: Estrogen plays a crucial role in adipose tissue homeostasis, influencing fat distribution, lipid metabolism, and insulin sensitivity. Through estrogen receptor (ER) activation, particularly ERα, estradiol (E2) regulates adipogenesis, inhibits adipocyte hypertrophy, promotes signaling. It enhances oxidation, reduces lipogenesis, suppresses pro-inflammatory cytokine production, thereby maintaining metabolic health. Primary ovarian insufficiency (POI), characterized by deficiency...

10.3390/metabo15040242 article EN cc-by Metabolites 2025-04-02

Lack of exon 3 the GH receptor (d3-GHR) has been associated with increased responsiveness to therapy. By analogy, we hypothesized that patients acromegaly bearing d3-GHR genotype may have a more morbid clinical and biochemical picture.Our objective was determine whether GHR genotype, by modifying tissue sensitivity GH, influences clinical/biochemical expression its outcome after treatment.The study conducted at specialized clinic tertiary care hospital.We prospective investigation...

10.1210/jc.2008-0391 article EN The Journal of Clinical Endocrinology & Metabolism 2008-07-09

Somatostatin analogs (SA) have been used for over 25 years in the treatment of acromegaly. A major disadvantage is need to continue therapy indefinitely.To evaluate feasibility discontinuing well-controlled patients with acromegaly treated chronically SA.Of 205 subjects on octreotide LAR, we selected those who met following criteria: two or more treatment, a stable dose and injection interval 20 mg every 8 weeks longer previous year, no history radiation, cabergoline 6 months, GH <1.5 ng/ml,...

10.1530/eje-11-0738 article EN European Journal of Endocrinology 2011-10-13

Object. According to a recent consensus statement on the treatment of acromegaly, its biochemical cure is defined as normalization age- and sex-adjusted insulin-like growth factor (IGF)—I levels suppression hormone (GH) by glucose lower than 1 ng/ml. The present study was prompted clinical observation that many cases acromegaly can be considered cured according one criterion but not others at different moments in patient's postoperative course. Methods. Fifty-three patients with (30 women 23...

10.3171/jns.2002.97.2.0287 article EN Journal of neurosurgery 2002-08-01

Summary Background The definition of biochemical cure in acromegaly involves both the normalization IGF‐1 and a glucose‐suppressed GH level &lt; 1 ng/ml. These criteria were reached by several consensus meetings, although no evidence‐based recommendations as to optimal time perform evaluations made, nor was fact that patients may change biochemically upon long‐term follow‐up taken into consideration. Objectives To identify characterize changes acromegaly. Patients methods One hundred...

10.1111/j.1365-2265.2006.02430.x article EN Clinical Endocrinology 2006-01-20

&lt;i&gt;Objective:&lt;/i&gt; To analyze clinical-biochemical correlations in newly diagnosed acromegaly, focusing particular on patients with discrepant parameters. &lt;i&gt;Design:&lt;/i&gt; Retrospective study. &lt;i&gt;Methods:&lt;/i&gt; Data from 164 acromegaly seen between 1995 and 2003. Patients were reviewed for the presence of headaches, arthralgias, hypertension, menstrual abnormalities, impotence, glucose intolerance or diabetes. Biochemical evaluation consisted age-...

10.1159/000082032 article EN Hormone Research in Paediatrics 2004-01-01

Abstract Context Acromegaly registries constitute a valuable source of therapeutic outcome information in real-life. Objective The objective this work is to analyze surgical and pharmacological outcomes the Mexican Registry (MAR). Design Methods Data were extracted from MAR informatic platform. Surgical remission was defined by postoperative postglucose (GH) less than 1 ng/mL an insulin-like growth factor (IGF-1) 1.2 × upper limit normal (ULN). Pharmacological basal GH IGF-1 ULN. Results A...

10.1210/clinem/dgaa664 article EN The Journal of Clinical Endocrinology & Metabolism 2020-09-18

Abstract Context The term micromegaly has been used to describe a subset of patients who have elevated IGF-1 levels but apparently normal basal GH (bGH) concentrations and often glucose-suppressed &amp;lt;1 ng/mL. Objective To evaluate the prevalence, clinical spectrum, therapeutic outcome acromegaly with bGH at diagnosis. Design Methods Retrospective analysis cohort diagnosed treated tertiary care center. Results A 528 was stratified according diagnosis: group 1, &amp;lt;2 ng/mL, n = 16; 2,...

10.1210/jc.2018-01113 article EN The Journal of Clinical Endocrinology & Metabolism 2018-07-27

Abstract Background Pituitary adenomas (PA) are the second most common intracranial tumors and classified according to hormone they produce, transcription factors express. The majority of PA occur sporadically, their molecular pathogenesis is incompletely understood. Methods Here we performed transcriptome proteome analysis derived from POU1F1 (GH-, TSH-, PRL-tumors, N = 16), NR5A1 (gonadotropes null cells adenomas, n 17) TBX19 (ACTH-tumors, 6) lineages as well silent ACTH-tumors (n 3)...

10.1186/s12920-022-01206-y article EN cc-by BMC Medical Genomics 2022-03-08
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