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1.
Rev. biol. trop ; 72(supl.1): e59008, Mar. 2024. tab, graf
Article in Spanish | LILACS, SaludCR | ID: biblio-1559334

ABSTRACT

Resumen Introducción: Los equinoideos irregulares se caracterizan por tener una selección del sustrato en fondos blandos principalmente. En El Salvador se han registrado siete especies de equinoideos irregulares en las principales playas arenosas del país, M. stokesii es una de ellas. Objetivo: Determinar la abundancia, densidad y estructura de tallas, en playones de la bocana del estero El Tamarindo, El Salvador. Métodos: La investigación se realizó en época seca en el oriente del país en playones del estero El Tamarindo que se caracteriza por presentar grandes extensiones de arena mezclada con materia orgánica. En cada sitio, se trazaron transectos en banda paralelos a la costa mediante 9 cuadrantes de 10 m2 separados entre sí por 10 m (área total de 90 m2), en donde se contabilizaron y midieron los individuos de M. stokesii que se encontraran dentro del área delimitada. Resultados: Se contabilizaron 958 individuos de M. stokesii con una densidad total de 10.64 ± 13.22 ind/m2. El rango de tamaños fue de 1-6.5 cm. El hábitat se caracterizó por presentar arena con materia orgánica en los primeros mm del sustrato en compañía de otros invertebrados. Conclusiones: La abundancia y densidad de M. stokesii es similar a la registrada en otros estudios de la región.


Abstract Introduction: Irregular echinoids are characterized by having a selection of the substrate mainly on soft bottoms. In El Salvador, seven species of irregular echinoids have been recorded on the main sandy beaches of the country, M. stokesii is one of them. Objective: Determine the abundance, density and size structure of M. stokesii on beaches at the mouth of the El Tamarindo estuary, El Salvador. Methods: The research was carried out in the dry season in the east of the country on the beaches of the El Tamarindo estuary, which is characterized by large extensions of sand mixed with organic matter. At each site, band transects parallel to the coast were plotted by 9 quadrants of 10 m2 separated from each other by 10 m (total area of 90 m2), where individuals of M. stokesii found within the delimited area were counted and measured. Results: 958 individuals of M. stokesii were counted with a total density of 10.64 ± 13.22 ind/m2. The size range was 1-6.5 cm. The habitat was characterized by presenting sand with organic matter in the first mm of the substrate in the company of other invertebrates. Conclusions: The abundance and density of M. stokesii are similar to the ones recorded in other studies in the region.


Subject(s)
Animals , Sea Urchins/classification , Ecosystem , Sampling Studies , El Salvador
2.
J Clin Endocrinol Metab ; 107(9): e3594-e3602, 2022 08 18.
Article in English | MEDLINE | ID: mdl-35789387

ABSTRACT

BACKGROUND: Lipoprotein(a) (Lp(a)) is a significant cardiovascular risk factor. Knowing the mechanisms that regulate its concentration can facilitate the development of Lp(a)-lowering drugs. This study analyzes the relationship between triglycerides (TGs) and Lp(a) concentrations, cross-sectionally and longitudinally, and the influence of the number and composition of TG-rich lipoproteins, and the APOE genotype. METHODS: Data from Aragon Workers Health Study (AWHS) (n = 5467), National Health and Nutrition Examination Survey III phase 2 (n = 3860), and Hospital Universitario Miguel Servet (HUMS) (n = 2079) were used for cross-sectional TG and Lp(a) relationship. Lp(a) intrasubject variation was studied in AWHS participants and HUMS patients with repeated measurements. TG-rich lipoproteins were quantified by nuclear magnetic resonance in a subsample from AWHS. Apolipoproteins B and E were quantified by Luminex in very low-density lipoprotein (VLDL) isolated by ultracentrifugation, from HUMS samples. APOE genotyping was carried in AWHS and HUMS participants. Regression models adjusted for age and sex were used to study the association. RESULTS: The 3 studies showed an inverse relationship between TG and Lp(a). Increased VLDL number, size, and TG content were associated with significantly lower Lp(a). There was an inverse association between the apoE concentration in VLDL and Lp(a). No significant association was observed for apolipoprotein (apo)B. Subjects carrying the apoE2/E2 genotype had significantly lower levels of Lp(a). CONCLUSION: Our results show an inverse relationship Lp(a)-TG. Subjects with larger VLDL size have lower Lp(a), and lower values of Lp(a) were present in patients with apoE-rich VLDL and apoE2/E2 subjects. Our results suggest that bigger VLDLs and VLDLs enriched in apoE are inversely involved in Lp(a) plasma concentration.


Subject(s)
Lipoprotein(a) , Lipoproteins, VLDL , Apolipoprotein E2 , Apolipoproteins B , Apolipoproteins E/genetics , Cross-Sectional Studies , Humans , Nutrition Surveys , Triglycerides/metabolism
3.
Am J Med Genet C Semin Med Genet ; 172(2): 198-205, 2016 06.
Article in English | MEDLINE | ID: mdl-27164022

ABSTRACT

Cornelia de Lange Syndrome (CdLS) is an autosomal dominant (NIPBL, SMC3, and RAD21) or X-linked (SMC1A and HDAC8) disorder, characterized by distinctive craniofacial appearance, growth retardation, intellectual disability, and limb anomalies. In 2005, the Spanish CdLS Reference Center was started and now we have more than 270 cases in our database. In this special issue, we describe some of the unique or atypical patients studied by our group, whose clinical features have contributed to the expansion of the CdLS classical phenotype, helping clinicians to diagnose it. We include the case of a male with unilateral tibial hypoplasia and peroneal agenesis who had a mutation in NIPBL; we also describe one patient with a mutation in NIPBL and somatic mosaicism identified by new generation sequencing techniques; we also include one patient with CdLS and Turner syndrome; and last, an interesting patient with a duplication of the SMC1A gene. Finally, we make a short review of the splicing mutations we have found in NIPBL regarding the new knowledge on the physiological variants of the gene. © 2016 Wiley Periodicals, Inc.


Subject(s)
De Lange Syndrome/genetics , Cell Cycle Proteins , De Lange Syndrome/diagnosis , De Lange Syndrome/pathology , Genetic Association Studies , Humans , Male , Proteins/genetics , Spain
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