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Biology subjects

Scholtens, D. M.

Publications and source records attributed to Scholtens, D. M..

3 recordsLinked to original sources

SpiderLearner: An ensemble approach to Gaussian graphical model estimation

Multivariate biological data are often modeled using networks in which nodes represent a biological variable (e.g., genes) and edges represent associations (e.g., coexpression). A Gaussian graphical model (GGM), or partial correlation network, is an undirected graphical model in which a weighted edge between two nodes represents the magnitude of their partial correlation, and the absence of an edge indicates zero partial correlation. A GGM provides a roadmap of direct dependencies between variables, providing a valuable systems-level perspective. Many methods exist for estimating GGMs; estimated GGMs are typically highly sensitive to choice of method, posing an outstanding statistical challenge. We address this challenge by developing SpiderLearner, a tool that combines a range of candidate GGM estimation methods to construct an ensemble estimate as a weighted average of results from each candidate. In simulation studies, SpiderLearner performs better than or comparably to the best of the candidate methods. We apply SpiderLearner to estimate a GGM for gene expression in a publicly available dataset of 260 ovarian cancer patients. Using the community structure of the GGM, we develop a network-based risk score which we validate in six independent datasets. The risk score requires only seven genes, each of which has important biological function. Our method is flexible, extensible, and has demonstrated potential to identify de novo biomarkers for complex diseases. An open-source implementation of our method is available at https://github.com/katehoffshutta/SpiderLearner.

bioinformatics↗

Women with isolated fasting hyperglycemia in pregnancy are at a higher genetic risk for type 2 diabetes

BackgroundUsing genetic scores for fasting plasma glucose (FPG GS) and type 2 diabetes (T2D GS), we investigated whether the fasting, 1-hour and 2-hour glucose thresholds from the WHO 2013 criteria for gestational diabetes (GDM) have different implications for genetic susceptibility to raised fasting glucose and type 2 diabetes in women from the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) and Atlantic Diabetes in Pregnancy (DIP) studies. MethodsCases were divided into three subgroups: (i) FPG [&ge;]5.1 mmol/L only, n=222; (ii) 1-hour glucose post 75 g oral glucose load [&ge;]10 mmol/L only, n=154 (iii) 2-hour glucose [&ge;]8.5 mmol/L only, n=73); and (iv) both FPG [&ge;]5.1 mmol/L and either of a 1-hour glucose [&ge;]10 mmol/L or 2-hour glucose [&ge;]8.5 mmol/L, n=172. We compared the FPG and T2D GS of these groups with controls (n=3,091) in HAPO and DIP separately. ResultsIn HAPO and DIP, the mean FPG GS in women with a FPG [&ge;]5.1 mmol/L, either on its own or with 1-hour glucose [&ge;]10 mmol/L or 2-hour glucose [&ge;]8.5 mmol/L, was higher than controls (all P <0.01). Mean T2D GS in women with a raised FPG alone or with either a raised 1-hour or 2-hour glucose was higher than controls (all P <0.05). GDM defined by 1-hour or 2-hour hyperglycaemia only was also associated with a higher T2D GS than controls (all P <0.05). ConclusionsThe different diagnostic categories that are part of the WHO 2013 criteria for GDM identify women with a genetic predisposition to type 2 diabetes as well as a risk for adverse pregnancy outcomes.

genetics↗

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

The duration of pregnancy is influenced by fetal and maternal genetic and non-genetic factors. We conducted a fetal genome-wide association meta-analysis of gestational duration, and early preterm, preterm, and postterm birth in 84,689 infants. One locus on chromosome 2q13 was associated with gestational duration; the association was replicated in 9,291 additional infants (combined P = 3.96 x 10-14). Analysis of 15,536 mother-child pairs showed that the association was driven by fetal rather than maternal genotype. Functional experiments showed that the lead SNP, rs7594852, alters the binding of the HIC1 transcriptional repressor. Genes at the locus include several interleukin 1 family members with roles in pro-inflammatory pathways that are central to the process of parturition. Further understanding of the underlying mechanisms will be of great public health importance, since giving birth either before or after the window of term gestation is associated with increased morbidity and mortality.

genetics↗