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Neurotensin Gene rs2234762 C>G Variant Associates with Reduced Circulating Pro-NT Levels and Predicts Lower Insulin Resistance in Overweight/Obese Children

Sentinelli, Federica (författare)
University of L'Aquila,Sapienza University of Rome
Barchetta, Ilaria (författare)
Sapienza University of Rome
Cimini, Flavia Agata (författare)
Sapienza University of Rome
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Dule, Sara (författare)
Sapienza University of Rome
Bailetti, Diego (författare)
Sapienza University of Rome,University of L'Aquila
Cossu, Efisio (författare)
University of Cagliari
Barbonetti, Arcangelo (författare)
University of L'Aquila
Totaro, Maria (författare)
University of L'Aquila
Melander, Olle (författare)
Lund University,Lunds universitet,Kardiovaskulär forskning - hypertoni,Forskargrupper vid Lunds universitet,Cardiovascular Research - Hypertension,Lund University Research Groups,Skåne University Hospital
Cavallo, Maria Gisella (författare)
Sapienza University of Rome
Baroni, Marco Giorgio (författare)
University of L'Aquila,Istituto Neurologico Mediterraneo Neuromed
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 (creator_code:org_t)
2023-03-30
2023
Engelska.
Ingår i: International Journal of Molecular Sciences. - : MDPI AG. - 1661-6596 .- 1422-0067. ; 24:7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Neurotensin (NT) is a small protein implicated in the regulation of energy balance which acts as both a neurotransmitter in the central nervous system and as a gastrointestinal peptide. In the gut, NT is secreted after fat ingestion and promotes the absorption of fatty acids. The circulating levels of its precursor, pro-NT, predicts the presence and development of metabolic and cardiovascular diseases. Despite the extensive knowledge on the dynamic changes that occur to pro-NT = after fat load, the determinants of fasting pro-NT are unknown. The aim of this study was to determine the possible genetic regulation of plasma pro-NT. The NT gene (NTS) was sequenced for potential functional variants, evaluating its entire genomic and potentially regulatory regions, in DNA from 28 individuals, stratified by low and high pro-NT levels. The identified variant differently distributed in the two pro-NT subgroups was genotyped in a cohort of nine hundred and thirty-two overweight/obese children and adolescents. A total of seven sequence variations across the NTS gene, none of them located in coding regions, were identified. The rs2234762 polymorphism, sited in the NTS gene promoter, was statistically more frequent in the lowest pro-NTS level group. Carriers of the rs2234762 variant showed lower pro-NT levels, after adjusting for sex, age, BMI, triglycerides and the Tanner stage. Having NTS rs2234762 predicted less pronounced insulin resistance at the 6.5-year follow-up with OR: 0.46 (0.216–0.983), at the logistic regression analysis adjusted for age, sex and BMI. In conclusion, the NTS rs2234762 gene variant is a determinant of reduced circulating pro-NT levels in overweight and obese children, which predisposes this group to a more favorable metabolic profile and a reduced insulin resistance later in life, independently from metabolic confounders.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

blood lipids
children
gastrointestinal peptides
gene
insulin resistance
neurotensin
obesity
single nucleotide polymorphism

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art (ämneskategori)
ref (ämneskategori)

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