Almudena Sánchez Villegas

Almudena Sánchez Villegas


Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 January 2010 in Nature Genetics
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Journal Article
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JDJosée Dupuis
Josée Dupuis
CLClaudia Langenberg
Claudia Langenberg
IPInga Prokopenko
Inga Prokopenko
RSRicha Saxena
Richa Saxena
NSNicole Soranzo
Nicole Soranzo
IBInês Barroso
Inês Barroso
The MAGIC investigators report results of a large genome-wide association study meta-analysis to identify common variants influencing fasting glucose homeostasis. They further show that several of the newly discovered loci influencing glycemic traits are also associated with risk of type 2 diabetes. Levels of circulating glucose are tightly regulated. To identify new loci influencing glycemic traits, we performed meta-analyses of 21 genome-wide association studies informative for fasting glucose, fasting insulin and indices of beta-cell function (HOMA-B) and insulin resistance (HOMA-IR) in up to 46,186 nondiabetic participants. Follow-up of 25 loci in up to 76,558 additional subjects identified 16 loci associated with fasting glucose and HOMA-B and two loci associated with fasting insulin and HOMA-IR. These include nine loci newly associated with fasting glucose (in or near ADCY5, MADD, ADRA2A, CRY2, FADS1, GLIS3, SLC2A2, PROX1 and C2CD4B) and one influencing fasting insulin and HOMA-IR (near IGF1). We also demonstrated association of ADCY5, PROX1, GCK, GCKR and DGKB-TMEM195 with type 2 diabetes. Within these loci, likely biological candidate genes influence signal transduction, cell proliferation, development, glucose-sensing and circadian regulation. Our results demonstrate that genetic studies of glycemic traits can identify type 2 diabetes risk loci, as well as loci containing gene variants that are associated with a modest elevation in glucose levels but are not associated with overt diabetes.

13 January 2008 in Nature Genetics
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Journal Article
Closed access
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CWCristen J Willer
Cristen J Willer
SSSerena Sanna
Serena Sanna
AJAnne U Jackson
Anne U Jackson
ASAngelo Scuteri
Angelo Scuteri
LBLori L Bonnycastle
Lori L Bonnycastle
GAGonçalo R Abecasis
Gonçalo R Abecasis

1 September 1997 in Osteoporosis International
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Journal Article
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MCM.-C. Chapuy
M.-C. Chapuy
PPP. Preziosi
P. Preziosi
MMM. Maamer
M. Maamer
SAS. Arnaud
S. Arnaud
PGPilar Galan
Pilar Galan
PMP.J. Meunier
P.J. Meunier

10 May 2009 in Nature Genetics
Verified
Journal Article
Open access
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WCWellcome Trust Case Control Consortium
Wellcome Trust Case Control Consortium
CNChristopher Newton-Cheh
Christopher Newton-Cheh
TJToby Johnson
Toby Johnson
VGVesela Gateva
Vesela Gateva
MTMartin D Tobin
Martin D Tobin
PMPatricia B Munroe
Patricia B Munroe
Christopher Newton-Cheh and colleagues report a genome-wide association study for blood pressure traits as part of the Global BPgen consortium. They report eight loci with replicated association to systolic and/or diastolic blood pressure, with each also showing association to hypertension. Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood pressure has proven challenging. We tested 2.5 million genotyped and imputed SNPs for association with systolic and diastolic blood pressure in 34,433 subjects of European ancestry from the Global BPgen consortium and followed up findings with direct genotyping (N ≤ 71,225 European ancestry, N ≤ 12,889 Indian Asian ancestry) and in silico comparison (CHARGE consortium, N = 29,136). We identified association between systolic or diastolic blood pressure and common variants in eight regions near the CYP17A1 (P = 7 × 10−24), CYP1A2 (P = 1 × 10−23), FGF5 (P = 1 × 10−21), SH2B3 (P = 3 × 10−18), MTHFR (P = 2 × 10−13), c10orf107 (P = 1 × 10−9), ZNF652 (P = 5 × 10−9) and PLCD3 (P = 1 × 10−8) genes. All variants associated with continuous blood pressure were associated with dichotomous hypertension. These associations between common variants and blood pressure and hypertension offer mechanistic insights into the regulation of blood pressure and may point to novel targets for interventions to prevent cardiovascular disease.

13 May 2012 in Nature Genetics
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AMAlisa K Manning
Alisa K Manning
MHMarie-France Hivert
Marie-France Hivert
RSRobert A Scott
Robert A Scott
JGJonna L Grimsby
Jonna L Grimsby
NBNabila Bouatia-Naji
Nabila Bouatia-Naji
CLClaudia Langenberg
Claudia Langenberg

26 September 2018 in Molecular Psychiatry
Verified
Journal Article
Open access
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CLCamille Lassale
Camille Lassale
GBG. David Batty
G. David Batty
ABAmaria Baghdadli
Amaria Baghdadli
FJFelice Jacka
Felice Jacka
AVAlmudena Sánchez Villegas
Almudena Sánchez Villegas
TATasnime Akbaraly
Tasnime Akbaraly
With depression being the psychiatric disorder incurring the largest societal costs in developed countries, there is a need to gather evidence on the role of nutrition in depression, to help develop recommendations and guide future psychiatric health care. The aim of this systematic review was to synthesize the link between diet quality, measured using a range of predefined indices, and depressive outcomes. Medline, Embase and PsychInfo were searched up to 31st May 2018 for studies that examined adherence to a healthy diet in relation to depressive symptoms or clinical depression. Where possible, estimates were pooled using random effect meta-analysis with stratification by observational study design and dietary score. A total of 20 longitudinal and 21 cross-sectional studies were included. These studies utilized an array of dietary measures, including: different measures of adherence to the Mediterranean diet, the Healthy Eating Index (HEI) and Alternative HEI (AHEI), the Dietary Approaches to Stop Hypertension, and the Dietary Inflammatory Index. The most compelling evidence was found for the Mediterranean diet and incident depression, with a combined relative risk estimate of highest vs. lowest adherence category from four longitudinal studies of 0.67 (95% CI 0.55–0.82). A lower Dietary Inflammatory Index was also associated with lower depression incidence in four longitudinal studies (relative risk 0.76; 95% CI: 0.63–0.92). There were fewer longitudinal studies using other indices, but they and cross-sectional evidence also suggest an inverse association between healthy diet and depression (e.g., relative risk 0.65; 95% CI 0.50–0.84 for HEI/AHEI). To conclude, adhering to a healthy diet, in particular a traditional Mediterranean diet, or avoiding a pro-inflammatory diet appears to confer some protection against depression in observational studies. This provides a reasonable evidence base to assess the role of dietary interventions to prevent depression. This systematic review was registered in the PROSPERO International Prospective Register of Systematic Reviews under the number CRD42017080579.