The SardiNIA study population cohort comprises over 7,000 subjects, starting at ages from 14-102, from a cluster of four towns in Sardinia. The study has been measuring >600 quantitative traits (endophenotypes or quantitative risk-related genetic or environmental factors) that can be scored on a continuous scale, and is designed as a longitudinal studies, with 4 visits over the first 15 years of its tenure. Traits of special interest include a range of cardiovascular risk factors, anthropometric measurements, blood test values, and facets of personality. Fourth visits have been completed for the study cohort to permit more incisive assessment of longitudinal trends and outcomes, as well as the assessment of additional phenotypes related to bone density and frailty as a function of age. For example, 24 hour blood pressure measurements and ECHOcardiography are extending the analysis of cardiovascular traits; hearing tests and retinograms are extending studies to sensory deficits in aging; and the cohort has been specifically extended to over 250 individuals over 92 years of age to analyze effects of extreme age. With this cohort, a variety of epidemiological and genetic factors have been identified, including recent epidemiological studies have been done of personality traits associated with white coat or masked hypertension, with circadian blood pressure patterns, or with uric acid levels; of the prevalence of chronic kidney disease and unknown thyroid disorders; and of arterial stiffness and influences of the metabolic syndrome. Full-genome DNA sequencing and genotyping with specialized chips (metabochip, immunochip, and exome chip, and a chip designed to give equal coverage across the entire genome). The whole cohort has also been analyzed to yield genetic variation data down to allelic frequencies of 0.1% 23,107,086 single nucleotide polymorphisms (SNP) and 3,053,323 insertions/deletions (indels) available for the analysis of genetic factors in traits and autoimmune diseases. GWAS pointed to genes/variants that determine a significant portion of the genetic contribution to variance for each trait and disease. In conjunction with consortium efforts on other population cohorts, including the Baltimore Longitudinal Study of Aging and the InCHIANTI study supported by the NIA, an increasing number of publications have resulted that identify genes associated with obesity, cardiovascular traits, and levels of lipids and blood components. GWAS consortium studies have also advanced technical approaches, including the usefulness of averaging of quantitative blood pressure traits; quality control; integrative annotation of variants; and mining the human phenome using allelic scores. As for GWAS of genetic factors involved in traits and diseases, Consortium efforts in the last year have discovered variants associated with obesity affected by smoking, and with plasma osmolality. In a new initiative, we are deepening the analysis of sensory capacity, with completed analyses of hearing tests and ongoing studies of microvasculature in retinal photographs. Those have detailed age-related changes that often correlate with disease phenotypes. In recent years, GWAS findings have been reported for several traits in three Nature Genetics papers: Two new gene variants were found to have a significant effect on stature in Sardinians. Together, they appear to reduce height by 6 centimeters. Lipids and Inflammation -- We identified 14 novel genetic variants associated with serum lipid levels, as well as 19 associated with inflammatory markers in the blood. Both lipid levels and inflammatory markers influence risk of heart disease. For the first time, researchers concurrently analyzed gene regulation of A1, A2 and fetal hemoglobin levels, to see if there was any coordination in their regulation. Twenty-three associations were seen at 10 loci, including five new gene candidates. Half the variants showed associations with more than one type of hemoglobin. An auxiliary approach, cohorts of Sardinian patients and controls were assembled and genotyped for GWAS for each of several diseases, Type 1 diabetes, multiple sclerosis (MS), and breast cancer. This has permitted our report in the New England Journal of Medicine an important factor in MS risk. In an ongoing initiative we FACS characterized cell ratios and expression of cell surface markers -- assessed as median fluorescence intensity (MFI) -- of helper T cell and cytotoxic T cells, regulatory T cells, B cells, monocyte cells, and dendritic cells, resulting in 730 quantitative immune cell traits in 3,757 SardiNIA individuals. Correlating the quantitative immune cell traits mentioned above with our ultra-dense genetic map yielded a total of 67 associated loci correlated with autoimmunity. (manuscript in preparation). We have extended the studies to range of related measures, including published data on C-reactive protein monocyte chemotactic protein-1 (MCP-1), interleukin-6 (IL-6), adiponectin, and soluble BAFF. Furthermore, we have measured the circulating levels of the main immunoglobulin types (IgM, IgG and IgA) using both turbidimetric and Luminex assays in individuals from the same cohort, and saw 18 genome-wide associations.
| Luchetti, Martina; Sutin, Angelina R; Delitala, Alessandro et al. (2018) Personality traits and facets linked with self-reported alcohol consumption and biomarkers of liver health. Addict Behav 82:135-141 |
| Olivieri, Anna; Sidore, Carlo; Achilli, Alessandro et al. (2017) Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past. Mol Biol Evol 34:1230-1239 |
| Böger, Carsten A; Gorski, Mathias; McMahon, Gearoid M et al. (2017) NFAT5 andSLC4A10Loci Associate with Plasma Osmolality. J Am Soc Nephrol 28:2311-2321 |
| Hinney, A; Kesselmeier, M; Jall, S et al. (2017) Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Mol Psychiatry 22:321-322 |
| Justice, Anne E (see original citation for additional authors) (2017) Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat Commun 8:14977 |
| Qian, Yong; Butler, Thomas J; Opsahl-Ong, Krista et al. (2017) fastMitoCalc: an ultra-fast program to estimate mitochondrial DNA copy number from whole-genome sequences. Bioinformatics 33:1399-1401 |
| Steri, Maristella; Orrù, Valeria; Idda, M Laura et al. (2017) Overexpression of the Cytokine BAFF and Autoimmunity Risk. N Engl J Med 376:1615-1626 |
| Pala, Mauro; Zappala, Zachary; Marongiu, Mara et al. (2017) Population- and individual-specific regulatory variation in Sardinia. Nat Genet 49:700-707 |
| Hinney, A; Kesselmeier, M; Jall, S et al. (2017) Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Mol Psychiatry 22:192-201 |
| Barban, Nicola (see original citation for additional authors) (2016) Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet 48:1462-1472 |
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