Preventing alpelisib-related hyperglycaemia in HR+/HER2-/PIK3CA-mutated advanced breast cancer using metformin (METALLICA): a multicentre, open-label, single-arm, phase 2 trial.

Background: Hyperglycaemia is an early and frequent adverse event during alpelisib treatment. METALLICA aimed to evaluate prophylactic metformin to prevent or reduce hyperglycaemia occurrence in patients with HR+/HER2-/PIK3CA-mutated advanced breast cancer (ABC). Methods: Between August 13th, 2020 and March 23rd, 2022, this 2-cohort, phase 2, multicentre, single-arm trial (NCT04300790) enrolled patients with HR+/HER2-/PIK3CA-mutated ABC: cohort A, normal glycaemia (fasting plasma glucose <100 mg/dL [<5.6 mmol/L] and HbA1c <5.7%), and cohort B, prediabetes (fasting plasma glucose 100-140 mg/dL [5.6-7.8 mmol/L] and/or haemoglobin A1C [HbA1c] 5.7-6.4%). Participants were at least 18 years old, with Eastern Cooperative Oncology Group performance status of 0-1, and up to two prior lines of endocrine therapy (ET) for ABC. Alpelisib plus ET were administered in 28-day cycles after initiation of prophylactic metformin plus ET. Primary endpoint was the incidence of grade 3-4 hyperglycaemia over the first 8 weeks. Secondary endpoints included safety, progression-free survival (PFS), objective response rate (ORR), and clinical benefit rate (CBR). The primary objective for cohort A and B is met with ≤7 (14.6%) and ≤4 (20%) patients with grade 3-4 hyperglycaemia over the first 8 weeks, respectively. Findings: 233 patients were screened, and 68 (20.2%) patients were enrolled in cohorts A (n = 48) and B (n = 20). Median follow-up was 7.8 months (IQR 1.4-19.6). Over the first 8 weeks, one (2.1%) of 48 patients in cohort A (95% CI: 0.5-11.1; P < 0.0001), and three (15.0%) of 20 patients in cohort B (95% CI: 5.6-37.8; P = 0.016) had grade 3-4 hyperglycaemia. Serious treatment-related adverse events occurred in seven patients (10.3%). The most common were rash (two [2.9%]), vomiting (two [2.9%]), and diarrhoea (two [2.9%]). Discontinuation of alpelisib caused by AEs was reported in nine patients (13.2%), none caused by hyperglycaemia. At data cutoff (15 June, 2022), no treatment-related deaths were observed. In the full analysis set, median PFS was 7.3 months (95% CI: 5.9-not reached), ORR was 20.6% (95% CI: 11.7-32.1%), and CBR was 52.9% (95% CI: 40.4-65.2). Interpretation: In HR+/HER2-/PIK3CA-mutated ABC, prophylactic metformin before alpelisib plus endocrine treatment has low incidence and severity of alpelicib-induced hyperglycaemia. Funding: Novartis Pharmaceuticals.

First-Line Ipatasertib, Atezolizumab, and Taxane Triplet for Metastatic Triple-Negative Breast Cancer: Clinical and Biomarker Results.

PURPOSE: To evaluate a triplet regimen combining immune checkpoint blockade, AKT pathway inhibition, and (nab-) paclitaxel as first-line therapy for locally advanced/metastatic triple-negative breast cancer (mTNBC). PATIENTS AND METHODS: The single-arm CO40151 phase Ib study (NCT03800836), the single-arm signal-seeking cohort of IPATunity130 (NCT03337724), and the randomized phase III IPATunity170 trial (NCT04177108) enrolled patients with previously untreated mTNBC. Triplet therapy comprised intravenous atezolizumab 840 mg (days 1 and 15), oral ipatasertib 400 mg/day (days 1-21), and intravenous paclitaxel 80 mg/m2 (or nab-paclitaxel 100 mg/m2; days 1, 8, and 15) every 28 days. Exploratory translational research aimed to elucidate mechanisms and molecular markers of sensitivity and resistance. RESULTS: Among 317 patients treated with the triplet, efficacy ranged across studies as follows: median progression-free survival (PFS) 5.4 to 7.4 months, objective response rate 44% to 63%, median duration of response 5.6 to 11.1 months, and median overall survival 15.7 to 28.3 months. The safety profile was consistent with the known toxicities of each agent. Grade ≥3 adverse events were more frequent with the triplet than with doublets or single-agent paclitaxel. Patients with PFS >10 months were characterized by NF1, CCND3, and PIK3CA alterations and increased immune pathway activity. PFS <5 months was associated with CDKN2A/CDKN2B/MTAP alterations and lower predicted phosphorylated AKT-S473 levels. CONCLUSIONS: In patients with mTNBC receiving an ipatasertib/atezolizumab/taxane triplet regimen, molecular characteristics may identify those with particularly favorable or unfavorable outcomes, potentially guiding future research efforts.

Physical dependence in older adults and job burnout in their informal caregivers in the COVID-19 context, a correlational study / Dependencia física en personas adultas mayores y sobrecarga en sus cuidadores informales en el contexto de la pandemia por COVID-19, un estudio correlacional / Dependência física em idosos e sobrecarga em seus cuidadores informais no contexto da pandemia de COVID-19, um estudo correlacional

Introduction: The functional status of older adults (OA) is usually used as an indicator of their health. Increased dependence raises the need for an informal caregiver (IC), leading to a state of work overload, which was frequently observed during the COVID-19 confinement. Objective: To assess the relationship between physical dependence of OA, job burnout of their IC, and the confinement conditions in the context of the COVID-19 pandemic. Materials and methods: The participants included 77 OA together with their respective IC. The OA filled out a sociodemographic data sheet and a Confinement Conditions Questionnaire. In addition to these two forms, the IC filled out the Zarit Caregiver Burnout Scale and the ABVD Barthel Scale. Results: Statistically significant correlations were found between: physical dependence and job burnout (rho=0.475, p<0.01); physical dependence and confinement degree (rho=0.441, p<0.01); and job burden and confinement degree (rho=0.344, p<0.01). Conclusion: Caregivers develop a greater job burnout as a consequence of the OA's dependence. Furthermore, it seems that this burnout is more related to the confinement conditions experienced by older adults than to the caregiver's own conditions.

Introducción: El estado funcional de las personas adultas mayores (PAM) suele tomarse como indicador de salud; la presencia de dependencia incrementa la necesidad de un cuidador informal (CI) que puede desarrollar sobrecarga, lo cual se agudizó durante el confinamiento por COVID-19. Objetivo: Evaluar la relación de la dependencia física de las PAM, la sobrecarga de su CI y las condiciones de confinamiento en el contexto de la pandemia por COVID-19. Materiales y métodos: Participaron 77 diadas conformadas por una PAM y su CI. Las PAM contestaron una ficha de datos sociodemográficos y Cuestionario de Condiciones de Confinamiento. Los CI, diligenciaron una ficha de datos sociodemográficos, Cuestionario de Condiciones de Confinamiento, Escala de Carga del Cuidador de Zarit y Escala de Barthel de ABVD. Resultados: Se encontró correlaciones estadísticamente significativas entre la dependencia física y la sobrecarga (rho=0,475, p<0,01); la dependencia física y el grado de confinamiento (rho=0,441, p<0,01); y la sobrecarga y el grado de confinamiento (rho=0,344, p<0,01). Conclusión: Los cuidadores de PAM desarrollan mayor sobrecarga frente a su dependencia física; además parece ser que la sobrecarga del cuidador está más relacionada con las condiciones de confinamiento de las personas adultas mayores, que con las propias condiciones de confinamiento del cuidador.

Introdução: O estado funcional do idoso (PAM) é geralmente tomado como um indicador de saúde; A presença de dependência aumenta a necessidade de um cuidador informal (CI) que pode desenvolver sobrecarga, que se agravou durante o confinamento da COVID-19. Objetivo: Avaliar a relação entre a dependência física dos PAM, a sobrecarga do seu CI e as condições de confinamento no contexto da pandemia de COVID-19. Materiais e métodos: Participaram 77 díades compostas por uma PAM e seu CI. O PAM respondeu a uma ficha de dados sociodemográficos e a um Questionário de Condições de Confinamento. Os CI preencheram ficha de dados sociodemográficos, Questionário de Condições de Confinamento, Escala de Sobrecarga do Cuidador de Zarit e Escala Barthel (ABVD). Resultados: Foram encontradas correlações estatisticamente significativas entre dependência física e sobrecarga (rho=0,475, p<0,01); dependência física e grau de confinamento (rho=0,441, p<0,01); e sobrecarga e grau de confinamento (rho=0,344, p<0,01). Conclusão: Os cuidadores do PAM desenvolvem maior sobrecarga diante da dependência física; além disso, parece que a sobrecarga do cuidador está mais relacionada com as condições de confinamento dos idosos do que com as próprias condições de confinamento do cuidador.

Monocyte Activation and Ageing Biomarkers in the Development of Cardiovascular Ischaemic Events or Diabetes in People with HIV.

We investigated whether blood telomere length (TL), epigenetic age acceleration (EAA), and soluble inflammatory monocyte cytokines are associated with cardiovascular events or diabetes (DM) in people living with HIV (PLHIV). This was a case-control study nested in the Spanish HIV/AIDS Cohort (CoRIS). Cases with myocardial infarction, stroke, sudden death, or diabetes after starting antiretroviral therapy were included with the available samples and controls matched for sex, age, tobacco use, pre-ART CD4 cell count, viral load, and sample time-point. TL (T/S ratio) was analysed by quantitative PCR and EAA with DNA methylation changes by next-generation sequencing using the Weidner formula. Conditional logistic regression was used to explore the association with cardiometabolic events. In total, 180 participants (94 cases (22 myocardial infarction/sudden death, 12 strokes, and 60 DM) and 94 controls) were included. Of these, 84% were male, median (IQR) age 46 years (40-56), 53% were current smokers, and 22% had CD4 count ≤ 200 cells/mm3 and a median (IQR) log viral load of 4.52 (3.77-5.09). TL and EAA were similar in the cases and controls. There were no significant associations between TL, EAA, and monocyte cytokines with cardiometabolic events. TL and EAA were mildly negatively correlated with sCD14 (rho = -0.23; p = 0.01) and CCL2/MCP-1 (rho = -0.17; p = 0.02). We found no associations between TL, EAA, and monocyte cytokines with cardiovascular events or diabetes. Further studies are needed to elucidate the clinical value of epigenetic biomarkers and TL in PLHIV.

Impact of the 21-Gene Assay in Patients with High-Clinical Risk ER-Positive and HER2-Negative Early Breast Cancer: Results of the KARMA Dx Study.

BACKGROUND: The 21-gene Oncotype DX Breast Recurrence Score® assay is prognostic and predictive of chemotherapy benefit for patients with estrogen receptor-positive, HER2- early breast cancer (EBC). The KARMA Dx study evaluated the impact of the Recurrence Score® results (RS) on the treatment decision for patients with EBC and high-risk clinicopathological characteristics for whom chemotherapy (CT) was considered. METHODS: Eligible patients with EBC were candidates for the study if CT was considered standard recommendation by local guidelines. Three high-risk EBC cohorts were predefined: (A) pT1-2, pN0/N1mi, and grade 3; (B) pT1-2, pN1, and grades 1-2; and (C) neoadjuvant cT2-3, cN0, and Ki67 ≤ 30%. Treatment recommendations before and after 21-gene testing were registered, as well as treatment received and physicians' confidence levels in their final recommendations. RESULTS: A total of 219 consecutive patients were included from eight Spanish centers: 30 in cohort A, 158 in cohort B, and 31 in cohort C. Ten patients were excluded from the final analysis as CT was not initially recommended. After 21-gene testing, treatment decisions changed from CT + endocrine therapy (ET) to ET alone for 67% of the whole group. In total, 30% (95% confidence interval [CI] 15% to 49%), 73% (95% CI 65% to 80%), and 76% (95% CI 56% to 90%) of patients ultimately received ET alone in cohorts A, B, and C, respectively. Physicians' confidence in their final recommendations increased in 34% of cases. CONCLUSIONS: Use of the 21-gene test resulted in an overall 67% reduction in CT recommendation in patients considered candidates for CT. Our findings indicate the substantial potential of the 21-gene test to guide CT recommendations in patients with EBC considered to be at high risk of recurrence based on clinicopathological parameters, regardless of nodal status or treatment setting.

A Strategy for Magnetic and Electric Stimulation to Enhance Proliferation and Differentiation of NPCs Seeded over PLA Electrospun Membranes.

Neural progenitor cells (NPCs) have been shown to serve as an efficient therapeutic strategy in different cell therapy approaches, including spinal cord injury treatment. Despite the reported beneficial effects of NPC transplantation, the low survival and differentiation rates constrain important limitations. Herein, a new methodology has been developed to overcome both limitations by applying a combination of wireless electrical and magnetic stimulation to NPCs seeded on aligned poly(lactic acid) nanofibrous scaffolds for in vitro cell conditioning prior transplantation. Two stimulation patterns were tested and compared, continuous (long stimulus applied once a day) and intermittent (short stimulus applied three times a day). The results show that applied continuous stimulation promotes NPC proliferation and preferential differentiation into oligodendrocytic and neuronal lineages. A neural-like phenotypic induction was observed when compared to unstimulated NPCs. In contrast, intermittent stimulation patterns did not affect NPC proliferation and differentiation to oligodendrocytes or astrocytes morphology with a detrimental effect on neuronal differentiation. This study provides a new approach of using a combination of electric and magnetic stimulation to induce proliferation and further neuronal differentiation, which would improve therapy outcomes in disorders such as spinal cord injury.

Primary Chemoradiotherapy Treatment (PCRT) for HER2+ and Triple Negative Breast Cancer Patients: A Feasible Combination.

Primary systemic treatment (PST) downsizes the tumor and improves pathological response. The aim of this study is to analyze the feasibility and tolerance of primary concurrent radio−chemotherapy (PCRT) in breast cancer patients. Patients with localized TN/HER2+ tumors were enrolled in this prospective study. Radiation was delivered concomitantly during the first 3 weeks of chemotherapy, and it was based on a 15 fractions scheme, 40.5 Gy/2.7 Gy per fraction to whole breast and nodal levels I-IV. Chemotherapy (CT) was based on Pertuzumab−Trastuzumab−Paclitaxel followed by anthracyclines in HER2+ and CBDCA-Paclitaxel followed by anthracyclines in TN breast cancers patients. A total of 58 patients were enrolled; 25 patients (43%) were TN and 33 patients HER2+ (57%). With a median follow-up of 24.2 months, 56 patients completed PCRT and surgery. A total of 35 patients (87.5%) achieved >90% loss of invasive carcinoma cells in the surgical specimen. The 70.8% and the 53.1% of patients with TN and HER-2+ subtype, respectively, achieved complete pathological response (pCR). This is the first study of concurrent neoadjuvant treatment in breast cancer in which three strategies were applied simultaneously: fractionation of RT (radiotherapy) in 15 sessions, adjustment of CT to tumor phenotype and local planning by PET. The pCR rates are encouraging.

NPC transplantation rescues sci-driven cAMP/EPAC2 alterations, leading to neuroprotection and microglial modulation.

Neural progenitor cell (NPC) transplantation represents a promising treatment strategy for spinal cord injury (SCI); however, the underlying therapeutic mechanisms remain incompletely understood. We demonstrate that severe spinal contusion in adult rats causes transcriptional dysregulation, which persists from early subacute to chronic stages of SCI and affects nearly 20,000 genes in total tissue extracts. Functional analysis of this dysregulated transcriptome reveals the significant downregulation of cAMP signalling components immediately after SCI, involving genes such as EPAC2 (exchange protein directly activated by cAMP), PKA, BDNF, and CAMKK2. The ectopic transplantation of spinal cord-derived NPCs at acute or subacute stages of SCI induces a significant transcriptional impact in spinal tissue, as evidenced by the normalized expression of a large proportion of SCI-affected genes. The transcriptional modulation pattern driven by NPC transplantation includes the rescued expression of cAMP signalling genes, including EPAC2. We also explore how the sustained in vivo inhibition of EPAC2 downstream signalling via the intrathecal administration of ESI-05 for 1 week impacts therapeutic mechanisms involved in the NPC-mediated treatment of SCI. NPC transplantation in SCI rats in the presence and absence of ESI-05 administration prompts increased rostral cAMP levels; however, NPC and ESI-05 treated animals exhibit a significant reduction in EPAC2 mRNA levels compared to animals receiving only NPCs treatment. Compared with transplanted animals, NPCs + ESI-05 treatment increases the scar area (as shown by GFAP staining), polarizes microglia into an inflammatory phenotype, and increases the magnitude of the gap between NeuN + cells across the lesion. Overall, our results indicate that the NPC-associated therapeutic mechanisms in the context of SCI involve the cAMP pathway, which reduces inflammation and provides a more neuropermissive environment through an EPAC2-dependent mechanism.

Genomic and Transcriptomic Analyses of Breast Cancer Primaries and Matched Metastases in AURORA, the Breast International Group (BIG) Molecular Screening Initiative.

AURORA aims to study the processes of relapse in metastatic breast cancer (MBC) by performing multi-omics profiling on paired primary tumors and early-course metastases. Among 381 patients (primary tumor and metastasis pairs: 252 targeted gene sequencing, 152 RNA sequencing, 67 single nucleotide polymorphism arrays), we found a driver role for GATA1 and MEN1 somatic mutations. Metastases were enriched in ESR1, PTEN, CDH1, PIK3CA, and RB1 mutations; MDM4 and MYC amplifications; and ARID1A deletions. An increase in clonality was observed in driver genes such as ERBB2 and RB1. Intrinsic subtype switching occurred in 36% of cases. Luminal A/B to HER2-enriched switching was associated with TP53 and/or PIK3CA mutations. Metastases had lower immune score and increased immune-permissive cells. High tumor mutational burden correlated to shorter time to relapse in HR+/HER2- cancers. ESCAT tier I/II alterations were detected in 51% of patients and matched therapy was used in 7%. Integration of multi-omics analyses in clinical practice could affect treatment strategies in MBC. SIGNIFICANCE: The AURORA program, through the genomic and transcriptomic analyses of matched primary and metastatic samples from 381 patients with breast cancer, coupled with prospectively collected clinical data, identified genomic alterations enriched in metastases and prognostic biomarkers. ESCAT tier I/II alterations were detected in more than half of the patients.This article is highlighted in the In This Issue feature, p. 2659.

Comparative transcriptome analysis identifies CARM1 and DNMT3A as genes associated with osteoporosis.

To identify new candidate genes in osteoporosis, mainly involved in epigenetic mechanisms, we compared whole gene-expression in osteoblasts (OBs) obtained from women undergoing hip replacement surgery due to fragility fracture and severe osteoarthritis. Then, we analyzed the association of several SNPs with BMD in 1028 women. Microarray analysis yielded 2542 differentially expressed transcripts belonging to 1798 annotated genes, of which 45.6% (819) were overexpressed, and 54.4% (979) underexpressed (fold-change between - 7.45 and 4.0). Among the most represented pathways indicated by transcriptome analysis were chondrocyte development, positive regulation of bone mineralization, BMP signaling pathway, skeletal system development and Wnt signaling pathway. In the translational stage we genotyped 4 SNPs in DOT1L, HEY2, CARM1 and DNMT3A genes. Raw data analyzed against inheritance patterns showed a statistically significant association between a SNP of DNMT3A and femoral neck-(FN) sBMD and primarily a SNP of CARM1 was correlated with both FN and lumbar spine-(LS) sBMD. Most of these associations remained statistically significant after adjusting for confounders. In analysis with anthropometric and clinical variables, the SNP of CARM1 unexpectedly revealed a close association with BMI (p = 0.000082), insulin (p = 0.000085), and HOMA-IR (p = 0.000078). In conclusion, SNPs of the DNMT3A and CARM1 genes are associated with BMD, in the latter case probably owing to a strong correlation with obesity and fasting insulin levels.

Optogenetic Modulation of Neural Progenitor Cells Improves Neuroregenerative Potential.

Neural progenitor cell (NPC) transplantation possesses enormous potential for the treatment of disorders and injuries of the central nervous system, including the replacement of lost cells or the repair of host neural circuity after spinal cord injury (SCI). Importantly, cell-based therapies in this context still require improvements such as increased cell survival and host circuit integration, and we propose the implementation of optogenetics as a solution. Blue-light stimulation of NPCs engineered to ectopically express the excitatory light-sensitive protein channelrhodopsin-2 (ChR2-NPCs) prompted an influx of cations and a subsequent increase in proliferation and differentiation into oligodendrocytes and neurons and the polarization of astrocytes from a pro-inflammatory phenotype to a pro-regenerative/anti-inflammatory phenotype. Moreover, neurons derived from blue-light-stimulated ChR2-NPCs exhibited both increased branching and axon length and improved axon growth in the presence of axonal inhibitory drugs such as lysophosphatidic acid or chondroitin sulfate proteoglycan. Our results highlight the enormous potential of optogenetically stimulated NPCs as a means to increase neuroregeneration and improve cell therapy outcomes for enhancing better engraftments and cell identity upon transplantation in conditions such as SCI.

Ribociclib plus letrozole versus chemotherapy for postmenopausal women with hormone receptor-positive, HER2-negative, luminal B breast cancer (CORALLEEN): an open-label, multicentre, randomised, phase 2 trial.

BACKGROUND: In hormone receptor-positive, HER2-negative early stage breast cancer, cyclin-dependent kinases 4 and 6 (CDK4/6) inhibition in combination with endocrine therapy could represent an alternative to multiagent chemotherapy. We aimed to evaluate the biological and clinical activity of neoadjuvant ribociclib plus letrozole in the luminal B subtype of early stage breast cancer. METHODS: CORALLEEN is a parallel-arm, multicentre, randomised, open-label, phase 2 trial completed across 21 hospitals in Spain. We recruited postmenopausal women (≥18 years) with stage I-IIIA hormone receptor-positive, Eastern Cooperative Oncology Group Performance Status 0-1, HER2-negative breast cancer and luminal B by PAM50 with histologically confirmed, operable primary tumour size of at least 2 cm in diameter as measured by MRI. Patients were randomly assigned (1:1) using a web-based system and permuted blocks of 25 to receive either six 28-days cycles of ribociclib (oral 600 mg once daily for 3 weeks on, 1 week off) plus daily letrozole (oral 2·5 mg/day) or four cycles of doxorubicin (intravenous 60 mg/m2) and cyclophosphamide (intravenous 600 mg/m2) every 21 days followed by weekly paclitaxel (intravenous 80 mg/m2) for 12 weeks. The total duration of the neoadjuvant therapy was 24 weeks. Randomisation was stratified by tumour size and nodal involvement. Samples were prospectively collected at baseline (day 0), day 15, and surgery. The primary endpoint was to evaluate the proportion of patients with PAM50 low-risk-of-relapse (ROR) disease at surgery in the modified intention-to-treat population including all randomly assigned patients who received study drug and had a baseline and at least one post-baseline measurement of ROR score. The PAM50 ROR risk class integrated gene expression data, tumour size, and nodal status to define prognosis. This trial was registered at ClinicalTrials.gov, NCT03248427. FINDINGS: Between July 27, 2017 to Dec 7, 2018, 106 patients were enrolled. At baseline, of the 106 patients, 92 (87%) patients had high ROR disease (44 [85%] of 52 in the ribociclib and letrozole group and 48 [89%] of 54 in the chemotherapy group) and 14 (13%) patients had intermediate-ROR disease (eight [15%] and six [11%]). Median follow-up was 200·0 days (IQR 191·2-206·0). At surgery, 23 (46·9%; 95% CI 32·5-61·7) of 49 patients in the ribociclib plus letrozole group and 24 (46·1%; 32·9-61·5) of 52 patients in the chemotherapy group were low-ROR. The most common grade 3-4 adverse events in the ribociclib plus letrozole group were neutropenia (22 [43%] of 51 patients) and elevated alanine aminotransferase concentrations (ten [20%]). The most common grade 3-4 adverse events in the chemotherapy group were neutropenia (31 [60%] of 52 patients) and febrile neutropenia (seven [13%]). No deaths were observed during the study in either group. INTERPRETATION: Our results suggest that some patients with high-risk, early stage, hormone receptor-positive, HER2-negative breast cancer could achieve molecular downstaging of their disease with CDK4/6 inhibitor and endocrine therapy. FUNDING: Novartis, Nanostring, Breast Cancer Research Foundation-AACR Career Development Award.

Effect of roasting conditions on pigment composition and some quality parameters of pistachio oil.

Pistachio roasting before oil extraction increases consumer preference but may cause changes in the oil composition. In this work, the effect of different roasting conditions on the physical parameters, oxidative stability, and pigment composition of pistachio oil extracted by pressure was studied. Density value of pistachio oil was reduced with severe roasting conditions (125 °C), while viscosity increased slightly. This adverse effect was compensated by a significant increase in both oxidative stability and, especially, in the content of chlorophyll and carotenoid pigments. Pistachio roasting temperature had a clear impact on the color of the pistachio oils, changing from yellow in oils from raw or minimally roasted pistachios (50-75 °C) to brilliant green in oils from pistachios subjected to higher temperature treatments (100-125 °C). An increase in temperature favored the pigment transfer to the oil. The green oils had a total pigment content between 2.3 and 4 times higher than the yellow oils.

Composition of pigments and colour changes in green table olives related to processing type.

Brownish colourations in Natural green table olives (non-treated with alkali) make this product less attractive to consumers than Spanish-style green table olives (treated with alkali), which develop a more appreciated bright golden-yellow colour. These colour differences were studied in relation to changes in the composition of chlorophyll and carotenoid pigments, as well as polyphenolic compounds and polyphenol oxidase enzyme (PPO) activity. Natural green olives showed a different chlorophyll profile than Spanish-style. However, all the chlorophyll pigments formed in both processing types were Mg-free derivatives (mostly pheophytins) with similar colourations, ranging from grey to green brownish. In the carotenoid fraction no appreciable differences were found between both processing types. The fruit's brownish colour was mainly due to polymeric substances with a size of >1000 daltons and polyphenolic nature, resulting from an enzymatic oxidation by PPO of the o-diphenolic compounds present in the fresh fruits.

Factor de riesgo para suicidio según dos cuestionarios y factores asociados en población estudiantil de la Universidad de Manizales (Colombia), 2011 / Risk factor for suicide according to two questionnaires and factors linked to the student population of a university in Manizales (Colombia), 2011

El suicidio es una conducta producto de la interacción de muchas variables que llevan al ser humano a tratar de terminar con su vida por sus propios medios. Este estudio pretende identificar el factor de riesgo suicida; además de factores asociados en los estudiantes de pregrado de la Universidad de Manizales. Es un estudio de corte transversal, en el cual se seleccionó una muestra probabilística de 355 alumnos de programas de dicha universidad y se aplicaron los cuestionarios de Beck y Plutchik para riesgo suicida y factores asociados. El estudio mostró un factor de riesgo para suicidio según la Escala de Plutchik de 13,5% y según la Escala de Desesperanza de Beck entre riesgo suicida alto y moderado de un 16,7%. Y como factores asociados se encontraron significativos, según la Escala de Plutchik, el estrato socioeconómico (p= 0,005), presencia de un diagnóstico psiquiátrico (p=0,000), consumo de alcohol (p=0,000) y sustancias psicoactivas (p=0,000), antecedentes familiares de suicidio (p=0,034), funcionalidad familiar (p=0,000), nivel de autoestima (p=0,000), ansiedad (p=0,000) y depresión (p=0,000); según la Escala de Beck, además de los anteriores factores asociados, se encontró la asociación significativa con raza (p=0,003), estado civil (p=0,007), espiritualidad (p=0,000) y el programa de pregrado que se encuentre cursando el estudiante (p=0,000). El Factor de Riesgo para Suicidio, según Escala de Plutchik, es parecido al encontrado en otras poblaciones análogas. Las escalas de Plutchik y de Beck, aunque relacionadas, no son equivalentes.

Suicide is a conduct as a result of the interaction of many variables that lead a human being to end with his/her life through their own means. This study pretends to identify the suicidal risk factor and associated factors in undergraduate students of the Universidad de Manizales. This is a Cross-sectional study, of a probabilistic sample of 355 student of the undergraduate programs of the Universidad de Manizales. The student population that was studied consisted of three hundred and fifty five students. The Plutchik's Scale and Beck's Hopelessness Scale for suicide risk were employed, the associated factors also were measured. This study showed, according to Plutchik's Scale, a suicide risk factor of 13.5%, and a 16.7% of a high and moderate suicide risk factor according to Beck's Scale. The study also threw out important associated factors on the Plutchik's Scale: socioeconomic stratum (p= 0,005), psychiatric diagnosis (p= 0,000), intake of alcohol (p= 0,000) and psychoactive substances consumption (p=0,000), family members with suicidal background (p=0,034), family functionality (p= 0,000), self-esteem levels (p= 0,000), anxiety (p= 0,000) and depression (p= 0,000). In relation to Beck's Scale, besides the factors that were previously mentioned, the following were found race (p=0,003), marital status (p= 0,007), spirituality (p= 0,000), and the undergraduate program that each student is part of (p= 0,000). Plutchik Risk factor for suicide, is similar to that found in others similar populations. Plutchik and Beck scales are not equivalent but related.

Mathematical model to predict the formation of pyropheophytin a in virgin olive oil during storage.

A mathematical model has been developed that describes the changes of pyropheophytin a (pyphya) in virgin olive oil (VOO). The model has been created using multivariate statistical procedures and is used in the prediction of the stability and loss of freshness of VOO. An earlier thermokinetic study (Aparicio-Ruiz, R.; Mínguez-Mosquera, M. I.; Gandul-Rojas, B. Thermal degradation kinetics of chlorophyll pigments in virgin olive oils. 1. Compounds of series a. J. Agric. Food Chem.2010, 58, 6200-6208) that looked at the characterization of the degradation of pheophytin a (phya), the main chlorophyll compound in VOO and a precursor of pyphya, allowed the authors to obtain the kinetic parameters necessary for mathematically expressing the percentage of pyphya, according to the time and temperature of storage using the Arrhenius model. Data regarding the percentage of pyphya obtained during the actual degradation of VOO in darkness, at room temperature and with a limited supply of oxygen, has allowed the mathematical prediction model to be validated. Using average monthly temperatures in the calculation of kinetic constants, theoretical data are obtained that are generally found to be within 95% confidence levels of experimental data.

Control of olive oil adulteration with copper-chlorophyll derivatives.

The present work proposes an analytical method able to detect in an adulterated olive oil sample the addition of the copper complexes of chlorophylls (E 141i). The method consists of a pigment extraction in liquid phase and subsequent analysis by HPLC-DAD. The profile of chlorophyll pigments of an olive oil is determined essentially by its content in pheophytins (a and b), but in no case any copper derivative. Different samples of colorant E 141i have been analyzed, the natural coloring additives used to adulterate vegetable oils. The 99.59+/-0.52% of the chlorophyll pigments present in the different samples of E 141i colorant are not those of an olive oil (more than 75% are cupro-derivatives). Thus, the simple detection of one of the compounds in an olive oil indicates adulteration. The major chlorophyll derivative in all the E 141i colorants samples is Cu-pyropheophytin a and its limit of detection (LOD) defined at a signal-to-noise ratio of about 3 was 6.58 ng/g.

Experiencia clínica con Telbivudina en Hepatitis crónica B en Venezuela

De acuerdo a consensos científicos a nivel internacional el objetivo primordial en el tratamiento de la hepatitis crónica B (HCB) es actualmete lograr la supresión de la replicación viral de manera potente y en el menor tiempo posible. A continuación presentamos la experiencia clínica acumulada en Venezuela empleando el análogo nucleosido telbivudina en pacientes con HCB. Se analizaron 29 portadores con HCB, promedio de edad 44±17 años, con una proporción 2/1 sexo masculino/sexo femenino, 23 con HCB antígeno e positivo y 6 con HCB antígeno e negativo. Las variables escogidas de evaluación fueron la viremia (ADN VHB), el valor de ALT y la tolerancia al tratamiento. Durante un período promedio de tratamiento de 7,3 meses cada paciente recibió 600 mg diarios de telbivudina. 86,2% de ellos disminuyó significativamente la carga circulante de ADN VHB de 7,3±1,2 log10 copias/mL a 1,9±1,0 log10 copias/mL (p= 0,0001). Adicionalmente, se demostró disminución significativa de los valores de ALT, de un promedio de 4,3 veces a una media de 1,4 veces el límite superior normal (p=0,01). Exceptuando un paciente con elevación importante de creatin-quinasa y otro que se quejó de sensación de acidez, la tolerancia reportada fue muy buena. Es concluyente que la telbivudina indujo supresión de la carga viral en forma potente y temprana tanto en pacientes con HCB antígeno e positivo como antígeno e negativo, mejoró los valores de ALT y fue bien tolerada la dosis por la mayoría. La reducción de la carga viral a niveles incluso indetectables durante el primer año de tratamiento, debería contribuir a prevenir la emergencia temprana de cepas del VHB resistentes a esta droga antiviral.

According to international scientific consensus, the fundamental goal in the treatment of chronic hepatitis B (CHB) is currently to achieve suppression of the viral replication in a very potent way at the shortest possible time. It follows our clinical experience accomplished in Venezuela by using the nucleoside analog telbivudine in patients with CHB. We studied twenty-nine carriers with CHB, mean age of 44±17 years old, male/female ratio 2/1, 23 of them with e antigen positive CHB and the remaining 6 with e antigen negative CHB. We selected the viral load (HBV DNA), the ALT value and the treatment tolerance as the parameters to be assessed. During an average treatment period of 7,3 months each patient received 600 mg daily of telbivudine. 86.2% of them showed significant decreased of the circulating HBV DNA load, from 7.3±1.2 log10 copies/mL to 1.9±1.0 log10 copies/mL (p= 0.0001). In addition, a significant decrease of ALT values from a mean of 4.3 fold to 1.4 fold (p=0.01) was also demonstrated. The group of patients showed very good tolerance of the doses, except one who presented increased creatine kinase value and another one who complained from peptic symptoms. It is conclusive that Telbivudine induced early and potent viral suppression, either in e antigen positive or e antigen negative CHB, improved the ALT values and was very well-tolerated by the majority. The viral load reduction, even undetectable during the first year of treatment, should contribute to prevent the early emergency of resistant strains to this antiviral drug.

Transplante hepático pediátrico en Venezuela experiencia preliminar

Introducción y objetivos: el transplante hepático es uno de los tratamientos adecuados en pacientes pediátricos con enfermedades hepáticas en fase terminal. El objetivo del presente trabajo es presentar la experiencia preliminar del programa de transplante hepático pediátrico llevada a cabo en nuestro país. Pacientes y métodos: se incluyeron niños que fueron evaluados en la consulta de pretransplante pediátrico del programa metropolitano de transplante por presentar enfermedades hepáticas en fase terminal Resultados: se incluyeron pacientes a los que se les realizó transplante hepático entre abril de 2005 y marzo de 2007; 9 pacientes en edades comprendidas entre 5 años y 15 años, 3 del sexo masculino y 6 del sexo femenino. Todos los pacientes presentaban serología para CMV positiva previo al transplante y 5 presentaban serología positiva para EBV previa al transplante. Todos los individuos tenían una calificación PELD entre 9 y 17. La enfermedad hepática crónica que los llevó a la necesidad de realizarles transplante hepático incluyó los siguientes diagnósticos: atresia de vías biliares extrahepáticas4, colestasis intrahepática familiar progresiva² y hepatitis autoinmune¹, hepatocarcinoma¹ y fibrosis hepática congénita¹. A 7 de los pacientes se les realizó transplante hepático de donante vivo, 1 de donante cadavérico y 1 autotransplante. El tiempo de estadía en terapia intensiva fue de 11 a 30 días, y el tiempo posterior en hospitalización fue de 3 a 15 días. El esquema de inmunosupresión inicial fue ciclosporina, prednisona, micofenolato a 4 pacientes y 5 tacrolimus y prednisona. Dos pacientes presentaron rechazo agudo el cual fue tratado con bolus de esteroides por 3 días con resolución completa de la disfunción del injerto. Todos los pacientes presentaron complicaciones infecciosas en los primeros 6 meses del postransplante, entre ellas: 4 pacientes infecciones urinarias documentadas por urocultivo por Proteus Mirabilis 2 y E. Coli 2, 5 pacientes presentaron infecciones por CMV a los cuales se les administró valganciclovir por vía oral obteniendo una respuesta adecuada. Dos de los pacientes presentaron complicaciones neurológicas, 1 presentó convulsiones tónico clónicas generalizadas sin déficit neurológico, se le realizó TAC y EEG los cuales resultaron normales con niveles elevados de ciclosporina y niveles bajos de magnesio que fueron corregidos. Un paciente presentó alucinaciones, se le realizó TAC cerebral y EEG normal, recibió haloperidol durante un período de 3 meses, con evolución satisfactoria. Uno de los pacientes presentó complicación biliar a los 9 meses postransplante, demostrada por ecografía abdominal y colangioresonancia (estenosis de la vía biliar), se colocó prótesis biliar con mejoría completa del funcionalismo hepático. Un paciente con síndrome hepatopulmonar previo al transplante, amerito para su corrección final, después del trasplante de tratamiento endovascular del shunt AV, arteria pulmonar lóbulo inferior izquierdo con colocación de espirales de titanium con resolución de la hipoxemia persistente. Posteriormente, ese mismo paciente presentó vasoespasmo de la arteria hepática documentado por perdida del registro arterial durante evaluación doppler y acompañado de elevación de las aminotranferasas recibiendo tratamiento con nitroglicerina intrarterial y colocación de stent con mejoría completa del funcionalismo hepático. La sobrevida del injerto y de los pacientes es en la actualidad de un 100%. Conclusión: el transplante hepático constituye hoy en día en Venezuela una posibilidad terapéutica para los pacientes pediátricos con enfermedad hepática terminal, progresiva e irreversible, que no está exento de complicaciones pero que al ser diagnosticadas y tratadas a tiempo, alcanza un 100% de sobrevida tanto del injerto como de los pacientes.

Introduction and Objectives: Liver transplantation is the treatment of choice for pediatrics patients that suffer end stage liver disease (ESLD). The goal of this essay is to introduce the first national experience with the modality of liver pediatric transplantation programs in the treatment of ESLD in pediatrics patients. Patients and Methods: 9 children suffering ESLD and their respective donors were seen between April 2005 and May 2007, each patient and its donor underwent a complete transplant evaluation (cardiac, respiratory, renal evaluation, imaging studies, and blood work up) to determine their candidate for either liver transplant recipient, or liver donor. RESULTS: 9 patients in ages between 5 years and 15 years, 3 male and 6 were included. All the patients had positive serology for CMV before transplant and 5 had positive serology for EBV before transplant. All the patients had score PELD 9 and 17. Diagnoses of the recipients were as follow: 4 Atresias of extrahepatic biliary tract, 2 progressive familiar intrahepatic cholestasis, 1 autoimmune hepatitis, 1 congenital fibrosis and 1 hepatocarcinoma. 7 live donor liver transplants, 1 deceased donor and 1 autologous liver transplant were performed. Operative mortality was 0%. Patient and graft survival were 100% at 1 and 2 years follow up. Patients presented various complications that included: acute rejection, CMV infection, acute urinary tract infections, hepatic artery spasm, and seizures among others. All the previous mentioned complications were successfully treated. Conclusion: Liver transplant constitutes the best option for the patient with ESLD, early referral is critical in the outcome of pediatric patients that need liver transplant.

Manejo endoscópio de las complicaciones biliares post-transplante hepático experiencia en Venezuela / Biliary complications are present in 13% to 35% of patients who undergo liver transplantation. ERCP has been used as the endoscopic method to solve these problems. Objective: To show Venezuela's experience, using endoscopic therapy in biliary complications post orthotopic liver transplantation (OLT) including anastomotic stricture, fistula and anatomic distortion. Patients and methods: Since 2003, (16) orthotopic liver transplantations have been performed, 7 patients (43,75%) had biliary complications. ERCP was performed in all patients. Results: 3 of them presented biliary fistulas, 1 supra- anastomotic stricture, 1 anastomotic stricture and 2 cases with biliary anatomic distortion. Endoscopic sphincterotomy with biliary stenting was performed in 5 patients, sphincterotomy with balloon dilation and stenting in 1 patient and only sphincterotomy in 1 patient. There were no complications for the procedure and all the patients had good clinical outcome. Conclusions: Early diagnosis and early endoscopic therapy through ERCP are the most important tools to solve biliary complications following liver transplantation.

Las complicaciones biliares se presentan en 13 a 35% de los pacientes en quienes se realiza transplante hepático,siendo la CPRE un método endoscópico utilizado para su resolución. Objetivo: mostrar la experiencia en Venezuela del manejo endoscópico de las complicaciones biliares postransplante hepático ortotópico incluyendo estenosis anastomótica, fístula biliar y distorsión anatómica (acodamiento de la vía biliar). Pacientes y métodos: desde el año 2003 se realizaron 16 transplantes hepáticos ortotópicos presentándose complicaciones biliares en 7 de ellos (43,75%). Se realizó la CPRE en su totalidad. Resultados: se encontraron 3 casos de fístula biliar, 1 estenosis supraanastomótica, 1 casos de estenosis anastomótica y 2 casos de acodamiento de la vía biliar. Se realizó esfinterotomía endoscópica más colocación de prótesis biliar en 5 pacientes, esfinterotomía más dilatación con balón y colocación de prótesis en 1 paciente y esfinterotomía sola en 1 paciente. No hubo complicaciones por el procedimiento y los pacientes presentaron evolución satisfactoria. Conclusión: el diagnóstico y la realización precoz de procedimientos terapéuticos endoscópicos como la CPRE, constituyen herramientas fundamentales para la resolución de las complicaciones biliares postransplante hepático.