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1.
Eur J Cancer ; 136: 149-158, 2020 09.
Article in English | MEDLINE | ID: mdl-32688208

ABSTRACT

BACKGROUND: Enhanced recovery after surgery (ERAS) programs include multiple perioperative elements designed to achieve early recovery after surgery and a shorter length of stay (LOS) in hospital. The PROFAST trial aimed to expand the evidence base for implementing ERAS in advanced gynaecologic oncology surgery. METHODS: This prospective, interventional randomised clinical trial enrolled women undergoing surgery for either suspected or diagnosed advanced ovarian cancer, at a reference hospital in gynaecologic oncology in Barcelona (Spain) and who were treated after either an ERAS protocol or conventional management (CM) protocol. All enrolled women who underwent cytoreductive surgery were included in the primary analysis. The primary outcome was reduction in LOS, and secondary outcomes were incidence and type of intraoperative and postoperative complications, rate of readmission and mortality within a 30-d follow-up period. This trial is registered at ClinicalTrials.gov, number NCT02172638. FINDINGS: From June 2014 to March 2018, 110 women were recruited, of which eleven were excluded. The ERAS group comprised 50 patients, and the CM group, 49 patients. Both groups were comparable with respect to baseline characteristics and complexity of the cytoreductive surgery, with an overall medium/high Aletti surgical complexity score of 7.4. Overall compliance to the ERAS protocol was 92%. As compared with the patients in the CM group, patients in the ERAS group had a decreased median of LOS of two days (7 versus 9 days; p = 0.0099) and a decreased rate of readmission (6% versus 20%, p = 0.0334). No further significant differences were detected with respect to incidence of intraoperative or postoperative complications, severe (Clavien-Dindo grade IIIB-IV) complications, Comprehensive Complication Index, reoperation during primary stay, or mortality. INTERPRETATION: Patients with advanced ovarian cancer in the ERAS program had a decreased LOS and decreased rate of readmission as compared with those in CM, with no increased morbidity or mortality. This study provides important evidence for the benefits of ERAS management even for gynaecologic surgeries of medium/high complexity and suggests that ERAS should be a standard practice for cytoreductive surgeries for peritoneal carcinomatosis.


Subject(s)
Adenocarcinoma/surgery , Enhanced Recovery After Surgery , Gynecologic Surgical Procedures/methods , Ovarian Neoplasms/surgery , Adenocarcinoma/epidemiology , Adenocarcinoma/pathology , Adult , Aged , Cytoreduction Surgical Procedures/adverse effects , Cytoreduction Surgical Procedures/methods , Cytoreduction Surgical Procedures/statistics & numerical data , Disease Progression , Feasibility Studies , Female , Gynecologic Surgical Procedures/adverse effects , Gynecologic Surgical Procedures/statistics & numerical data , Humans , Implementation Science , Length of Stay/statistics & numerical data , Middle Aged , Morbidity , Mortality , Ovarian Neoplasms/epidemiology , Ovarian Neoplasms/pathology , Patient Readmission/statistics & numerical data , Perioperative Care/methods , Perioperative Care/statistics & numerical data , Peritoneal Neoplasms/epidemiology , Peritoneal Neoplasms/secondary , Peritoneal Neoplasms/surgery , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Reoperation/statistics & numerical data , Treatment Outcome
2.
PLoS One ; 10(12): e0145162, 2015.
Article in English | MEDLINE | ID: mdl-26695515

ABSTRACT

Iberian ham production includes both purebred (IB) and Duroc-crossbred (IBxDU) Iberian pigs, which show important differences in meat quality and production traits, such as muscle growth and fatness. This experiment was conducted to investigate gene expression differences, transcriptional regulation and genetic polymorphisms that could be associated with the observed phenotypic differences between IB and IBxDU pigs. Nine IB and 10 IBxDU pigs were slaughtered at birth. Morphometric measures and blood samples were obtained and samples from Biceps femoris muscle were employed for compositional and transcriptome analysis by RNA-Seq technology. Phenotypic differences were evident at this early age, including greater body size and weight in IBxDU and greater Biceps femoris intramuscular fat and plasma cholesterol content in IB newborns. We detected 149 differentially expressed genes between IB and IBxDU neonates (p < 0.01 and Fold-Change > 1. 5). Several were related to adipose and muscle tissues development (DLK1, FGF21 or UBC). The functional interpretation of the transcriptomic differences revealed enrichment of functions and pathways related to lipid metabolism in IB and to cellular and muscle growth in IBxDU pigs. Protein catabolism, cholesterol biosynthesis and immune system were functions enriched in both genotypes. We identified transcription factors potentially affecting the observed gene expression differences. Some of them have known functions on adipogenesis (CEBPA, EGRs), lipid metabolism (PPARGC1B) and myogenesis (FOXOs, MEF2D, MYOD1), which suggest a key role in the meat quality differences existing between IB and IBxDU hams. We also identified several polymorphisms showing differential segregation between IB and IBxDU pigs. Among them, non-synonymous variants were detected in several transcription factors as PPARGC1B and TRIM63 genes, which could be associated to altered gene function. Taken together, these results provide information about candidate genes, metabolic pathways and genetic polymorphisms potentially involved in phenotypic differences between IB and IBxDU pigs associated to meat quality and production traits.


Subject(s)
Adiposity/physiology , Genotype , Muscle Proteins , Muscle, Skeletal , Swine , Transcriptome/physiology , Animals , Muscle Proteins/biosynthesis , Muscle Proteins/genetics , Muscle, Skeletal/growth & development , Muscle, Skeletal/metabolism , Species Specificity , Swine/genetics , Swine/growth & development , Swine/metabolism
3.
Genet Sel Evol ; 47: 81, 2015 Oct 16.
Article in English | MEDLINE | ID: mdl-26475049

ABSTRACT

BACKGROUND: The increasing availability of DNA markers provides new metrics of inbreeding based on single nucleotide polymorphisms (SNPs), i.e. molecular inbreeding or the proportion of runs of homozygosity (ROH), as alternatives to traditional pedigree-based inbreeding coefficients. However, none of these metrics incorporate the length of ROH as an indicator of recent inbreeding. Novel inbreeding coefficients that incorporate length of ROH as a random variable with an associated density are investigated. METHODS: New inbreeding metrics based on the distribution of the length of ROH are proposed: (1) the Kolmolgorov-Smirnov test, (2) a function of the quantiles of the cumulative distribution function of an individual versus the population, and (3) fitting of an exponential distribution to ROH lengths (mean, variance, and the probability of drawing at random a ROH larger than a given threshold). The new inbreeding and pedigree-based metrics were compared using 217 sows of an Iberian line that belong to three groups: C1 (conservation), C2 (conservation derived from C1), and S (selected and derived from C1), with complete pedigrees and genotyped for 35,023 SNPs. RESULTS: Correlations between pedigree-based and the new genomic inbreeding coefficients ranged from 0.22 to 0.72 but most ranged from 0.60 to 0.70. The correlation between quantile chromosomal inbreeding coefficients (using molecular information of just one chromosome at the time) and chromosomal length was 0.84 (SE = 0.14), supporting the hypothesis that these coefficients incorporate information on ROH length as an indication of recent inbreeding. Kolmogorov-Smirnov and exponential chromosomal inbreeding coefficients were also correlated with chromosomal length (0.57). Chromosome 1 had the largest quantile ROH inbreeding coefficient (largest ROH sizes), whereas chromosome 10 had the lowest (shortest ROH sizes). Selection for lean growth increased ROH-based inbreeding coefficients for group S when compared to unselected groups C1 and C2. At the chromosomal level, this comparison showed that the level of autozygosity and the length of ROH for most of the autosomes increased in the selection line. CONCLUSIONS: Quantile and exponential probability inbreeding coefficients using ROH length as a random variable provide additional information about recent inbreeding compared to existing inbreeding coefficients such as molecular, pedigree-based or total ROH content inbreeding coefficients.


Subject(s)
Chromosomes, Mammalian/genetics , Swine/genetics , Algorithms , Animals , Homozygote , Inbreeding , Pedigree , Polymorphism, Single Nucleotide
4.
Genet Sel Evol ; 47: 1, 2015 Jan 17.
Article in English | MEDLINE | ID: mdl-25595431

ABSTRACT

BACKGROUND: The current availability of genotypes for very large numbers of single nucleotide polymorphisms (SNPs) is leading to more accurate estimates of inbreeding coefficients and more detailed approaches for detecting inbreeding depression. In the present study, genome-wide information was used to detect inbreeding depression for two reproductive traits (total number of piglets born and number of piglets born alive) in an ancient strain of Iberian pigs (the Guadyerbas strain) that is currently under serious danger of extinction. METHODS: A total of 109 sows with phenotypic records were genotyped with the PorcineSNP60 BeadChip v1. Inbreeding depression was estimated using a bivariate animal model in which the inbreeding coefficient was included as a covariate. We used two different measures of genomic inbreeding to perform the analyses: inbreeding estimated on a SNP-by-SNP basis and inbreeding estimated from runs of homozygosity. We also performed the analyses using pedigree-based inbreeding. RESULTS: Significant inbreeding depression was detected for both traits using all three measures of inbreeding. Genome-wide information allowed us to identify one region on chromosome 13 associated with inbreeding depression. This region spans from 27 to 54 Mb and overlaps with a previously detected quantitative trait locus and includes the inter-alpha-trypsin inhibitor gene cluster that is involved with embryo implantation. CONCLUSIONS: Our results highlight the value of high-density SNP genotyping for providing new insights on where genes causing inbreeding depression are located in the genome. Genomic measures of inbreeding obtained on a SNP-by-SNP basis or those based on the presence/absence of runs of homozygosity represent a suitable alternative to pedigree-based measures to detect inbreeding depression, and a useful tool for mapping studies. To our knowledge, this is the first study in domesticated animals using the SNP-by-SNP inbreeding coefficient to map specific regions within chromosomes associated with inbreeding depression.


Subject(s)
Genetic Fitness , Inbreeding , Reproduction/genetics , Sus scrofa/genetics , Animals , Female , Genome-Wide Association Study , Homozygote , Male , Polymorphism, Single Nucleotide , Quantitative Trait Loci , Swine
5.
Br J Nutr ; 111(4): 735-46, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24528940

ABSTRACT

Maternal energy restriction during pregnancy predisposes to metabolic alterations in the offspring. The present study was designed to evaluate phenotypic and metabolic consequences following maternal undernutrition in an obese pig model and to define the potential role of hypothalamic gene expression in programming effects. Iberian sows were fed a control or a 50 % restricted diet for the last two-thirds of gestation. Newborns were assessed for body and organ weights, hormonal and metabolic status, and hypothalamic expression of genes implicated in energy homeostasis, glucocorticoid function and methylation. Weight and adiposity were measured in adult littermates. Newborns of the restricted sows were lighter (P <0·01), but brain growth was spared. The plasma concentration of TAG was lower in the restricted newborns than in the control newborns of both the sexes (P <0·01), while the concentration of cortisol was higher in females born to the restricted sows (P <0·04), reflecting a situation of metabolic stress by nutrient insufficiency. A lower hypothalamic expression of anorexigenic peptides (LEPR and POMC, P <0·01 and P <0·04, respectively) was observed in females born to the restricted sows, but no effect was observed in the males. The expression of HSD11B1 gene was down-regulated in the restricted animals (P <0·05), suggesting an adaptive mechanism for reducing the harmful effects of elevated concentrations of cortisol. At 4 and 7 months of age, the restricted females were heavier and fatter than the controls (P< 0·01). Maternal feed restriction induces asymmetrical growth retardation and metabolic alterations in the offspring. Differences in gene expression at birth and higher growth and adiposity in adulthood suggest a female-specific programming effect for a positive energy balance, possibly due to overexposure to endogenous stress-induced glucocorticoids.


Subject(s)
Fetal Growth Retardation/metabolism , Hypothalamus/metabolism , Malnutrition/complications , Obesity/etiology , Pregnancy Complications , Prenatal Exposure Delayed Effects , Prenatal Nutritional Physiological Phenomena , 11-beta-Hydroxysteroid Dehydrogenase Type 1/genetics , 11-beta-Hydroxysteroid Dehydrogenase Type 1/metabolism , Adiposity , Animals , Birth Weight , Brain/growth & development , Down-Regulation , Energy Intake , Female , Fetal Growth Retardation/etiology , Fetal Growth Retardation/genetics , Growth , Hydrocortisone/metabolism , Male , Obesity/genetics , Obesity/metabolism , Pregnancy , Pregnancy Complications/genetics , Pregnancy Complications/metabolism , Pro-Opiomelanocortin/metabolism , Receptors, Leptin/metabolism , Sex Factors , Stress, Physiological/genetics , Swine , Triglycerides/blood , Weight Gain/genetics
6.
PLoS One ; 8(10): e78314, 2013.
Article in English | MEDLINE | ID: mdl-24205195

ABSTRACT

Maintaining genetic variation and controlling the increase in inbreeding are crucial requirements in animal conservation programs. The most widely accepted strategy for achieving these objectives is to maximize the effective population size by minimizing the global coancestry obtained from a particular pedigree. However, for most natural or captive populations genealogical information is absent. In this situation, microsatellites have been traditionally the markers of choice to characterize genetic variation, and several estimators of genealogical coefficients have been developed using marker data, with unsatisfactory results. The development of high-throughput genotyping techniques states the necessity of reviewing the paradigm that genealogical coancestry is the best parameter for measuring genetic diversity. In this study, the Illumina PorcineSNP60 BeadChip was used to obtain genome-wide estimates of rates of coancestry and inbreeding and effective population size for an ancient strain of Iberian pigs that is now in serious danger of extinction and for which very accurate genealogical information is available (the Guadyerbas strain). Genome-wide estimates were compared with those obtained from microsatellite and from pedigree data. Estimates of coancestry and inbreeding computed from the SNP chip were strongly correlated with genealogical estimates and these correlations were substantially higher than those between microsatellite and genealogical coefficients. Also, molecular coancestry computed from SNP information was a better predictor of genealogical coancestry than coancestry computed from microsatellites. Rates of change in coancestry and inbreeding and effective population size estimated from molecular data were very similar to those estimated from genealogical data. However, estimates of effective population size obtained from changes in coancestry or inbreeding differed. Our results indicate that genome-wide information represents a useful alternative to genealogical information for measuring and maintaining genetic diversity.


Subject(s)
Swine/genetics , Animals , Female , Genealogy and Heraldry , Genetics, Population/methods , Genome/genetics , Genome-Wide Association Study/methods , Genotype , Inbreeding/methods , Male , Microsatellite Repeats/genetics , Pedigree , Polymorphism, Single Nucleotide/genetics , Population Density
7.
PLoS One ; 8(6): e66398, 2013.
Article in English | MEDLINE | ID: mdl-23824082

ABSTRACT

The leptin (LEP) and its receptor (LEPR) regulate food intake and energy balance through hypothalamic signaling. However, the LEP-LEPR axis seems to be more complex and its expression regulation has not been well described. In pigs, LEP and LEPR genes have been widely studied due to their relevance. Previous studies reported significant effects of SNPs located in both genes on growth and fatness traits. The aim of this study was to determine the expression profiles of LEP and LEPR across hypothalamic, adipose, hepatic and muscle tissues in Iberian x Landrace backcrossed pigs and to analyze the effects of gene variants on transcript abundance. To our knowledge, non porcine LEPR isoforms have been described rather than LEPRb. A short porcine LEPR isoform (LEPRa), that encodes a protein lacking the intracellular residues responsible of signal transduction, has been identified for the first time. The LEPRb isoform was only quantifiable in hypothalamus while LEPRa appeared widely expressed across tissues, but at higher levels in liver, suggesting that both isoforms would develop different roles. The unique LEP transcript showed expression in backfat and muscle. The effects of gene variants on transcript expression revealed interesting results. The LEPRc.1987C>T polymorphism showed opposite effects on LEPRb and LEPRa hypothalamic expression. In addition, one out of the 16 polymorphisms identified in the LEPR promoter region revealed high differential expression in hepatic LEPRa. These results suggest a LEPR isoform-specific regulation at tissue level. Conversely, non-differential expression of LEP conditional on the analyzed polymorphisms could be detected, indicating that its regulation is likely affected by other mechanisms rather than gene sequence variants. The present study has allowed a transcriptional characterization of LEP and LEPR isoforms on a range of tissues. Their expression patterns seem to indicate that both molecules develop peripheral roles apart from their known hypothalamic signal transduction function.


Subject(s)
Leptin/genetics , Receptors, Leptin/genetics , Transcription, Genetic , Animals , Gene Expression , Polymorphism, Single Nucleotide , Promoter Regions, Genetic , Swine
8.
BMC Genet ; 13: 41, 2012 May 20.
Article in English | MEDLINE | ID: mdl-22607048

ABSTRACT

BACKGROUND: The traditional strategy to map QTL is to use linkage analysis employing a limited number of markers. These analyses report wide QTL confidence intervals, making very difficult to identify the gene and polymorphisms underlying the QTL effects. The arrival of genome-wide panels of SNPs makes available thousands of markers increasing the information content and therefore the likelihood of detecting and fine mapping QTL regions. The aims of the current study are to confirm previous QTL regions for growth and body composition traits in different generations of an Iberian x Landrace intercross (IBMAP) and especially identify new ones with narrow confidence intervals by employing the PorcineSNP60 BeadChip in linkage analyses. RESULTS: Three generations (F3, Backcross 1 and Backcross 2) of the IBMAP and their related animals were genotyped with PorcineSNP60 BeadChip. A total of 8,417 SNPs equidistantly distributed across autosomes were selected after filtering by quality, position and frequency to perform the QTL scan. The joint and separate analyses of the different IBMAP generations allowed confirming QTL regions previously identified in chromosomes 4 and 6 as well as new ones mainly for backfat thickness in chromosomes 4, 5, 11, 14 and 17 and shoulder weight in chromosomes 1, 2, 9 and 13; and many other to the chromosome-wide signification level. In addition, most of the detected QTLs displayed narrow confidence intervals, making easier the selection of positional candidate genes. CONCLUSIONS: The use of higher density of markers has allowed to confirm results obtained in previous QTL scans carried out with microsatellites. Moreover several new QTL regions have been now identified in regions probably not covered by markers in previous scans, most of these QTLs displayed narrow confidence intervals. Finally, prominent putative biological and positional candidate genes underlying those QTL effects are listed based on recent porcine genome annotation.


Subject(s)
Body Composition/genetics , Genetic Linkage , Growth/genetics , Quantitative Trait Loci , Swine/genetics , Animals , Chromosomes, Mammalian , Genetic Association Studies , Oligonucleotide Array Sequence Analysis , Phenotype , Polymorphism, Single Nucleotide
9.
Rev cuba salud trabajo ; 13(2)mayo- ago. 2012. tab, graf
Article in Spanish | CUMED | ID: cum-52593

ABSTRACT

Introducción: La calidad de vida laboral se relaciona con la percepción que el trabajador tiene de su salud, bienestar y satisfacción a través de todo lo relacionado con su entorno laboral. Objetivo: Identificar el nivel de satisfacción de la calidad de vida laboral percibida por los conductores de pasaje foráneo. Material y método: Estudio descriptivo transversal; se realizó un censo en una empresa de autotransporte de pasaje foráneo, con 18 conductores postureros masculinos, aplicando cuestionarios sociodemográficos y laborales, y el CVT-GOHISALO, instrumento empleado para medir la calidad de vida en el trabajo. Resultados: La edad promedio de los conductores fue de 45,11 (±8,88) años, antigüedad profesional 23,89 (±10,82) años y antigüedad laboral en la empresa 14 (±7,66) años. De acuerdo al instrumentos, las dimensiones percibidas con baja satisfacción fueron: soporte institucional para el trabajo, 72,22 por ciento (13); integración al puesto de trabajo, 61,11 por ciento (11); satisfacción por el trabajo, 55,56 por ciento (10); bienestar logrado a través del trabajo, 83,33 por ciento (15); desarrollo personal, 50 por ciento (9); y administración del tiempo libre, 94,44 por ciento (17). Sólo la de seguridad en el trabajo obtuvo un nivel de satisfacción media con 50 por ciento (9). Conclusiones: Encontramos una satisfacción baja en la calidad de vida laboral en los conductores postureros, resultado contrario al esperado, ya que la mayoría de las personas que se dedican a esta actividad es porque les gusta. No se encontró ninguna asociación significativa con las condiciones laborales. Los hallazgos sugieren realizar estudios comparativos entre conductores de base y postureros(AU)


Subject(s)
Adult , Middle Aged , Occupational Health , Working Conditions , Quality of Life , Job Satisfaction
10.
BMC Genomics ; 10: 636, 2009 Dec 29.
Article in English | MEDLINE | ID: mdl-20040109

ABSTRACT

BACKGROUND: Prolificacy is the most important trait influencing the reproductive efficiency of pig production systems. The low heritability and sex-limited expression of prolificacy have hindered to some extent the improvement of this trait through artificial selection. Moreover, the relative contributions of additive, dominant and epistatic QTL to the genetic variance of pig prolificacy remain to be defined. In this work, we have undertaken this issue by performing one-dimensional and bi-dimensional genome scans for number of piglets born alive (NBA) and total number of piglets born (TNB) in a three generation Iberian by Meishan F(2) intercross. RESULTS: The one-dimensional genome scan for NBA and TNB revealed the existence of two genome-wide highly significant QTL located on SSC13 (P < 0.001) and SSC17 (P < 0.01) with effects on both traits. This relative paucity of significant results contrasted very strongly with the wide array of highly significant epistatic QTL that emerged in the bi-dimensional genome-wide scan analysis. As much as 18 epistatic QTL were found for NBA (four at P < 0.01 and five at P < 0.05) and TNB (three at P < 0.01 and six at P < 0.05), respectively. These epistatic QTL were distributed in multiple genomic regions, which covered 13 of the 18 pig autosomes, and they had small individual effects that ranged between 3 to 4% of the phenotypic variance. Different patterns of interactions (a x a, a x d, d x a and d x d) were found amongst the epistatic QTL pairs identified in the current work. CONCLUSIONS: The complex inheritance of prolificacy traits in pigs has been evidenced by identifying multiple additive (SSC13 and SSC17), dominant and epistatic QTL in an Iberian x Meishan F(2) intercross. Our results demonstrate that a significant fraction of the phenotypic variance of swine prolificacy traits can be attributed to first-order gene-by-gene interactions emphasizing that the phenotypic effects of alleles might be strongly modulated by the genetic background where they segregate.


Subject(s)
Genome/genetics , Quantitative Trait Loci/genetics , Swine/genetics , Animals , Chromosome Mapping , Genotype , Humans , Male , Microsatellite Repeats/genetics , Polymorphism, Single Nucleotide/genetics
11.
Mamm Genome ; 14(9): 650-6, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14629115

ABSTRACT

We present a QTL genome scan for fatty acid composition in pigs. An F2 cross between Iberian x Landrace pigs and a regression approach fitting the carcass weight as a covariate for QTL identification was used. Chromosomes (Chrs) 4, 6, 8, 10, and 12 showed highly significant effects. The Chr 4 QTL influenced the linoleic content and both the fatty acid double-bond index and peroxidability index. In Chr 6 we found significant associations with the double-bond index and the unsaturated index of fatty acids. Chr 8 showed clear effects on the percentages of palmitic and palmitoleic fatty acids as well as the average chain length of fatty acids. In Chr 10 we detected a significant QTL for the percentage of myristic fatty acid, with an F value that was slightly above the genomewide threshold. The percentage of linolenic fatty acid was affected by a region on Chr 12. A nearly significant QTL for the content of gadoleic fatty acid was also detected in Chr 12. We also analyzed the genomic QTL distribution by a regression model that fits the backfat thickness as a covariate. Some of the QTL that were detected in our analysis could not be detected when the data were corrected by backfat thickness. This work shows how critical the selection of a covariate can be in the interpretation of results. This is the first report of a genome scan detection of QTL directly affecting fatty acid composition in pigs.


Subject(s)
Fatty Acids/analysis , Quantitative Trait Loci , Sus scrofa/genetics , Sus scrofa/metabolism , Animals , Chromosome Mapping , Fatty Acids/chemistry , Female , Genotype , Male , Phenotype
12.
Genet Sel Evol ; 34(4): 465-79, 2002.
Article in English | MEDLINE | ID: mdl-12270105

ABSTRACT

One QTL affecting backfat thickness (BF), intramuscular fat content (IMF) and eye muscle area (MA) was previously localized on porcine chromosome 6 in an F2 cross between Iberian and Landrace pigs. This work was done to study the effect of two positional candidate genes on these traits: H-FABP and LEPR genes. The QTL mapping analysis was repeated with a regression method using genotypes for seven microsatellites and two PCR-RFLPs in the H-FABP and LEPR genes. H-FABP and LEPR genes were located at 85.4 and 107 cM respectively, by linkage analysis. The effects of the candidate gene polymorphisms were analyzed in two ways. When an animal model was fitted, both genes showed significant effects on fatness traits, the H-FABP polymorphism showed significant effects on IMF and MA, and the LEPR polymorphism on BF and IMF. But when the candidate gene effect was included in a QTL regression analysis these associations were not observed, suggesting that they must not be the causal mutations responsible for the effects found. Differences in the results of both analyses showed the inadequacy of the animal model approach for the evaluation of positional candidate genes in populations with linkage disequilibrium, when the probabilities of the parental origin of the QTL alleles are not included in the model.


Subject(s)
Body Composition/genetics , Carrier Proteins/genetics , Chromosomes/genetics , Neoplasm Proteins , Receptors, Cell Surface , Swine/genetics , Animals , Chromosome Mapping , Fatty Acid-Binding Proteins , Genetic Variation , Genotype , Linkage Disequilibrium/genetics , Lipids/analysis , Microsatellite Repeats/genetics , Models, Genetic , Polymorphism, Restriction Fragment Length , Quantitative Trait, Heritable , Receptors, Leptin , Regression Analysis
13.
Med. interna Méx ; 14(2): 47-50, mar.-abr. 1998. tab
Article in Spanish | LILACS | ID: lil-241441

ABSTRACT

Antecedentes. La hipertensión arterial es un estado de resistencia a la insulina (RI); el metformin mejora la RI y disminuye las concentraciones de la hormona, por lo que el fármaco debe ser útil en el tratamiento de la hipertensión arterial. Material y métodos. Treinta pacientes adultos con hipertensión estadio I se dividieron en dos grupos de 15 pacientes cada uno; el grupo 1 recibió metformin, 850 mg c/12 horas más modificaciones al estilo de vida (MEV), y el grupo 2 solamente recibió indicaciones respecto a este último. En los dos grupos se midió la presión arterial, el peso, la talla, el índice cintura-cadera y se determinaron la glucosa, la urea y la creatinina séricas, así como el colesterol, triglicéridos y las transaminasas al inicio y al final de estudio, 90 días después. Resultados. Todos los pacientes del grupo 1 redujeron la presión arterial (p<0.0002), peso (p<0.005), índice cintura-cadera (p<0.005), colesterol (p<0.005) y triglicéridos (p<0.005). Solamente en 14 pacientes del grupo 2 se redujo la presión arterial (p<0.5), pero no se modificaron peso, índice cintura-cadera, colesterol ni triglicéridos. Cuando se compraron los dos grupos entre sí, se encontró una diferencia significativa de todos los parámetros en el grupo con metformin. Concluisones. Estos datos sugieren que el metformin combinado con modificaciones al estilo de vida es mejor que estas últimas solas en el control de la hipertensión estadio I


Subject(s)
Humans , Male , Female , Adult , Health Behavior , Hypertension/etiology , Insulin Resistance , Metformin/administration & dosage , Obesity/drug therapy , Obesity/physiopathology
14.
La Paz; MDSP/VPPFM; 1998. 317 p. graf.
Monography in Spanish | LILACS, LIBOCS, LIBOSP | ID: lil-231770

ABSTRACT

El objetivo de la investigación consiste en aprender de la experiencia, para mejorar, la ejecución de la LPP, de modo particular en temas considerados como principales; señalar recomendaciones de ajustes y mejoras en su implementación, recogiendo la dinámica que han generado en los municipios algunos temas de la Participación Popular, como la distritación municipal, el proceso social de introducción de las demandas, su programación y ejecución, los comités de vigilancia, el seguro de maternidad y niñez y los consejeros departamentales


Subject(s)
Municipal Management , Politics , /standards , Community Participation/legislation & jurisprudence , Bolivia
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