0000000000993226

AUTHOR

Luca Deiana

showing 12 related works from this author

Analysis of HLA-DQA, HLA-DQB frequencies in a group of Sardinian centenarians

2006

Human leukocyte antigen (HLA) alleles, regulating type and intensity of the immune response, might influence life expectancy. In previous case-control studies the authors have demonstrated that both HLA-DR and -DQ alleles are not associated with longevity in the Sardinian population. On the other hand, association studies are subjected (as part of the homogeneity of the population in terms of geographic origin) to a number of possible confounding factors. Therefore, the authors typed the HLA-DQA1 and HLA-DQB1 alleles in 24 sibs (age range 85 to 97) of 17 centenarians by PCR-SSP. Sib pair analysis showed non-significant differences between the observed and expected percentage of DQA* or DQB1…

GeneticsAged 80 and overAgingeducation.field_of_studymedia_common.quotation_subjectPopulationConfoundingLongevityLongevityAnalysis of HLA-DQA HLA-DQBHuman leukocyte antigenBiologyHLA-DQ alpha-ChainsHLA-DQ AntigensTraitHLA-DQ beta-ChainsHumansGeriatrics and GerontologyAlleleAllele sharingeducationAllelesmedia_commonGenetic association
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Activity of mannose-binding lectin in centenarians

2012

Summary We analyzed MBL2 gene variants in two cohorts of centenarians, octo-nonagenarians and nonagenarians, and in the general population, one from Sardinia Island (Italy), recruited in the frame of the AKea study, and another from Campania (southern Italy), to search for haplotypes related to longevity. We also assessed in vitro the effect of mannose-binding lectin (MBL) on various human cells at different stage of senescence. The frequency of high and null activity haplotypes was significantly lower, and the frequency of intermediate activity haplotype significantly higher in centenarians and in subjects between 80 and 99 years from both the cohorts as compared each to the general popula…

SenescenceAgingeducation.field_of_studymedia_common.quotation_subjectHaplotypePopulationSerum albuminLongevityLectinCell BiologyBiologybacterial infections and mycosesImmunologybiology.proteineducationGenemedia_commonMannan-binding lectinAging Cell
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Analysis of HLA-DRB1,DQA1,DQB1 haplotypes in Sardinian centenarians

2008

Some genetic determinants of longevity might reside in those polymorphisms for the immune system genes that regulate immune responses. Many longevity association studies focused their attention on HLA (the human MHC) polymorphisms, but discordant results have been obtained. Sardinians are a relatively isolate population and represent a suitable population for association studies. Some HLA-DR and DQ alleles form very stable haplotypes with a strong linkage disequilibrium. In a previous study on Sardinian centenarians we have suggested that HLA-DRB1 *15 allele might be marginally associated to longevity. HLA-DR,DQ haplotypes are in strong linkage disequilibrium and well conserved playing a ro…

musculoskeletal diseasesAgingLinkage disequilibriummedia_common.quotation_subjectGenes MHC Class IILongevityPopulationBiologyBiochemistryArticleHLA-DQ alpha-ChainsLinkage Disequilibrium03 medical and health sciences0302 clinical medicineEndocrinologyGene FrequencyHLA-DQ AntigensGeneticsHLA-DQ beta-ChainsHumansskin and connective tissue diseaseseducationMolecular BiologyHLA-DRB1Allele frequencyComputingMilieux_MISCELLANEOUS030304 developmental biologyGenetic associationmedia_commonAged 80 and overGeneticsLikelihood Functions0303 health scienceseducation.field_of_studyPolymorphism GeneticHLA-DQB1HaplotypeLongevityHLA-DR AntigensCell BiologyHaplotypesItalyHLA Longevity SardiniaMedicineHLA-DRB1 Chains030215 immunologyExperimental Gerontology
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Frequency of the HFE Gene Mutations in Five Italian Populations

2002

Abstract ABSTRACT Genetic hemochromatosis is an autosomal recessive disorder characterized by iron overload and a variety of clinical manifestations such as liver cirrhosis and arthropathy. It is the most common genetic disease of northern European populations. The principal gene responsible for hereditary hemochromatosis, designated HFE, is located on chromosome 6 in the HLA region. The single point mutation 845A, changing cysteine at position 282 to tyrosine (C282Y), in this gene has been identified as the main genetic basis of hereditary hemochromatosis. Two other mutations, 187G, a histidine to aspartate at amino acid 63 (H63D), and 193T, a serine to cysteine at amino acid 65 (S65C), ap…

GeneticsPoint mutationHistocompatibility Antigens Class IHaplotypeMembrane ProteinsChromosomeCell BiologyHematologyBiologyAmino Acid Substitution; Gene Frequency; Hemochromatosis; Hemochromatosis Protein; Histocompatibility Antigens Class I; Humans; Italy; Membrane ProteinsAmino Acid SubstitutionGene FrequencyItalyHereditary hemochromatosisMutation (genetic algorithm)HumansMolecular MedicineHemochromatosisAlleleHemochromatosis ProteinMolecular BiologyAllele frequencyGeneBlood Cells, Molecules, and Diseases
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Association between longevity and cytokine gene polymorphisms. A study in Sardinian centenarians

2004

Background and aims: Human longevity seems to be directly correlated with optimal functioning of the immune system, suggesting that some genetic determinants of longevity reside in those polymorphisms for the immune system genes which regulate immuneinflammatory responses, in particular cytokine gene polymorphisms. The frequency of − 174C single nucleotide polymorphism (SNP) in the promoter region of the interleukin(IL)-6 gene is increased in Italian male centenarians. Moreover, the frequency of − 1082G SNP at the 5′ flanking region of the IL-10 gene coding sequence is increased among male centenarians, and that of +874A SNP at the interferon (IFN)- γ gene was found more frequently in femal…

MaleAgingmedia_common.quotation_subjectLongevityPopulationSingle-nucleotide polymorphismEnvironmentBiologyPolymorphism Single NucleotideInterferon-gammaPolymorphism (computer science)HumansSNPAlleleeducationGeneAgedmedia_commonAged 80 and overeducation.field_of_studyInterleukin-6LongevityMiddle AgedInterleukin-10ItalyImmunologyCytokinesFemaleGene poolGeriatrics and Gerontology
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Association between the HLA-DR alleles and longevity: a study in Sardinian population

2003

Human longevity may be correlated with optimal functioning of the immune system, suggesting that genetic determinants of longevity also resides in those polymorphisms for the immune system genes that regulate immune responses as histocompatibility (HLA) antigens. However, conflicting results have been obtained. Some well planned and designed association studies performed in Caucasians suggest that longevity is associated with positive selection of alleles (i.e. HLA-DR11) or haplotypes (i.e. HLA-B8,DR3) that confer resistance to infectious diseases, respectively, via peptide presentation or via antigen non-specific control of immune response. Association studies are subjected to a number of …

MaleAgingmedia_common.quotation_subjectLongevityPopulationHuman leukocyte antigenBiologyBiochemistryEndocrinologyGeneticsHLA-DRHumansAlleleeducationMolecular BiologyAgedmedia_commonGenetic associationAged 80 and overGeneticseducation.field_of_studyHistocompatibility TestingHaplotypeLongevityHLA-DR AntigensCell BiologyHistocompatibilityItalyFemaleExperimental Gerontology
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Fetuin-A serum levels are not correlated to kidney function in long-lived subjects

2012

Objectives: Serum Fetuin A has been identified as an inhibitor of ectopic calcification. It is reduced in subjects with chronic kidney disease (CKD) and it has been proposed as a potential link between CKD and the higher prevalence of arterial calcification observed in these patients. During ageing both the stiffening of arterial wall due to calcification and a decline in kidney function are frequent. The aim of the study is to investigate if Fetuin A serum levels are associated with ageing and with AHSG T256S polymorphism. Moreover, we aim at investigate whether serum Fetuin A is correlated to kidney function in this setting of senescence. Design and Methods: 256 health long-lived subjects…

MaleSenescenceAgingmedicine.medical_specialtyFetuin Aalpha-2-HS-GlycoproteinClinical BiochemistryGene ExpressionRenal functionKidneyKidney Function TestsPolymerase Chain ReactionPolymorphism Single NucleotideEctopic calcificationElderlyInternal medicinemedicineHumansCystatin Ckidney functionAged 80 and overbiologybusiness.industryCalcinosisGeneral MedicineSerum Fetuin AKidney diseasemedicine.diseaseFetuinArterial calcificationSettore BIO/12 - Biochimica Clinica E Biologia Molecolare ClinicaAHSG T256S polymorphismEndocrinologyFetuin A Cystatin C Elderly Kidney disease AHSGCystatin CAHSGbiology.proteinKidney Failure ChronicFemalebusinessPolymorphism Restriction Fragment LengthCalcificationKidney disease
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Association between the HFE mutations and longevity: a study in Sardinian population

2003

Hereditary hemochromatosis is an HLA-linked inherited disease characterised by inappropriately high absorption of iron by the gastrointestinal mucosa. The cysteine-to-tyrosine substitution at codon 282 of the HFE encoding gene sequence is responsible for the disease, although other variants, as H63D and S65C, may modify the affinity of the protein for transferrin receptors. We have recently reported that C282Y mutation is significantly increased in very old (>90 years) Sicilian women, suggesting a role in attainment of longevity. In addition, an increase of H63D polymorphism was also observed in these women but the difference was not significant. To validate and extend these results we inve…

Malecongenital hereditary and neonatal diseases and abnormalitiesAgingIronLongevityPopulation geneticsTransferrin receptorBiologyPolymorphism (computer science)medicineHumansPoint MutationAlleleHemochromatosis ProteinHemochromatosisAgedAged 80 and overGeneticsPolymorphism GeneticHistocompatibility Antigens Class IMembrane Proteinsnutritional and metabolic diseasesMiddle Agedmedicine.diseaseItalyHereditary hemochromatosisMutation (genetic algorithm)CentenarianDevelopmental BiologyMechanisms of Ageing and Development
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Effect of interleukin-6 polymorphisms on human longevity: a systematic review and meta-analysis.

2008

Udgivelsesdato: 2009-Jan Several studies have assessed changes in frequency of -174 interleukin (IL)-6 single nucleotide polymorphism (SNP) with age. If IL-6 tracks with disability and age-related diseases, then there should be reduction, in the oldest old, of the frequency of homozygous GG subjects, who produce higher IL-6 levels. However, discordant results have been obtained. To explore the relationship between this polymorphism and longevity, we analyzed individual data on long-living subjects and controls from eight case-control studies conducted in Europeans, using meta-analysis. There was no significant difference in the IL-6 genotype between the oldest old and controls (Odds Ratio […

AgingGenotypemedia_common.quotation_subjectLongevityPhysiologySingle-nucleotide polymorphismBiologyEnvironmentBiochemistryPolymorphism Single NucleotideGene FrequencyPolymorphism (computer science)GenotypeOdds RatioSNPHumansMolecular BiologyAllele frequencymedia_commonGeneticsAged 80 and overInterleukin-6LongevityOdds ratioNeurologyMeta-analysismeta-analysis interleukin-6 polymorphismsBiotechnologyAgeing research reviews
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Cellular immune activation in Sardinian middle-aged, older adults and centenarians

2017

In addition to viral infections, malignant disorders, autoimmune diseases, and allograft rejection episodes, neopterin increases in older people where it is found to be predictive of overall mortality. Thus, the serum concentrations of this biomarker of systemic immune and inflammation activation, were measured in a small cohort of Sardinian middle-aged, older adults and centenarians. There was a significant positive correlation between neopterin concentrations and age with the subjects in the 95-year-old group with the highest values. Notably, the group of centenarians had neopterin values comparable to those of 80- and 90-year-old groups, and significantly lower than that of 95-year-old g…

Male0301 basic medicineAgingImmunosenescenceLongevityInflammationBiologyNeopterinBiochemistryMonocytes03 medical and health scienceschemistry.chemical_compoundEndocrinologyImmune systemGeneticCentenariansGeneticsmedicineHumansMacrophageCentenarianCytokineMolecular BiologyAgedSettore MED/04 - Patologia GeneraleAged 80 and overMacrophagesPteridinesMonocyteAge FactorsNeopterinCell BiologyImmunosenescenceMacrophage ActivationMiddle AgedInflammaging030104 developmental biologymedicine.anatomical_structureItalychemistryImmunologyCohortPteridineCytokinesBiomarker (medicine)FemaleInflammation Mediatorsmedicine.symptomBiomarkersExperimental Gerontology
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Carotid restenosis is associated with plasma ADMA concentrations in carotid endarterectomy patients

2011

Abstract Background: The aim of this work has been to study the association between plasma asymmetric dimethylarginine (ADMA) concentrations and carotid stenosis in a group of 64 patients undergoing carotid endarterectomy (CEA). Methods: Arginine, ADMA and symmetric dimethylarginine (SDMA) were measured using capillary electrophoresis with UV detection. An evaluation of plasma concentrations of total cysteine (tCys) and total homocysteine (tHcy) was also performed. Results: Pearson’s analysis show a positive correlation between ADMA and carotid stenosis (r=0.37, p=0.003), which is also confirmed after stepwise multiple linear regression analysis. ADMA plasma concentrations were significantl…

Carotid Artery DiseasesMalemedicine.medical_specialtyArginineHomocysteinemedicine.medical_treatmentClinical BiochemistryCarotid endarterectomyArginineCohort Studiesrestenosischemistry.chemical_compoundRestenosisInternal medicinemedicineHumansCysteineHomocysteineAgedEndarterectomyEndarterectomy Carotidbusiness.industryBiochemistry (medical)General MedicineMiddle Agedmedicine.diseaseADMAStenosisSettore BIO/12 - Biochimica Clinica E Biologia Molecolare ClinicachemistryCardiologyRegression AnalysisFemaleMultiple linear regression analysisAsymmetric dimethylargininebusinesscarotid endarterectomycclm
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Activity of mannose-binding lectin in centenarians

2012

We analyzed MBL2 gene variants in two cohorts of centenarians, octo-nonagenarians and nonagenarians, and in the general population, one from Sardinia Island (Italy), recruited in the frame of the AKea study, and another from Campania (southern Italy), to search for haplotypes related to longevity. We also assessed in vitro the effect of mannose-binding lectin (MBL) on various human cells at different stage of senescence. The frequency of high and null activity haplotypes was significantly lower, and the frequency of intermediate activity haplotype significantly higher in centenarians and in subjects between 80 and 99 years from both the cohorts as compared each to the general population fro…

Aged 80 and overMalehaplotypeshaplotypesenescencemannose binding lectinLongevityagingAge FactorsAGING HAPLOTYPES INNATE IMMUNITY MANNOSE.BINDING LECTIN SENESCENCEbacterial infections and mycosesArticleCohort StudiesMannose-Binding LectinsHaplotypesHumansFemaleinnate immunityCells Cultured
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