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      Interaction between rs10830962 polymorphism in MTNR1B and lifestyle intervention on maternal and neonatal outcomes: secondary analyses of the DALI lifestyle randomized controlled trial

      1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 8 , 9 , 9 , , , , , , , , , , , , , , , , , , , , , , , DALI Core Investigator Group
      The American Journal of Clinical Nutrition
      Oxford University Press (OUP)

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          ABSTRACT

          Background

          Interactions between polymorphisms of the melatonin receptor 1B (MTNR1B) gene and lifestyle intervention for gestational diabetes have been described. Whether these are specific for physical activity or the healthy eating intervention is unknown.

          Objectives

          The aim was to assess the interaction between MTNR1B rs10830962 and rs10830963 polymorphisms and lifestyle interventions during pregnancy.

          Methods

          Women with a BMI (in kg/m2) of ≥29 (n = 436) received counseling on healthy eating (HE), physical activity (PA), or both. The control group received usual care. This secondary analysis had a factorial design with comparison of HE compared with no HE and PA compared with no PA. Maternal outcomes at 24–28 wk were gestational weight gain (GWG), maternal fasting glucose, insulin, insulin resistance (HOMA-IR), disposition index, and development of GDM. Neonatal outcomes were cord blood leptin and C-peptide and estimated neonatal fat percentage. The interaction between receiving either the HE or PA intervention and genotypes of both rs10830962 and rs10830963 was assessed using multilevel regression analysis.

          Results

          GDM risk was increased in women homozygous for the G allele of rs10830962 (OR: 2.60; 95% CI: 1.34, 5.06) or rs10830963 (OR: 2.83; 95% CI: 1.24, 6.47). Significant interactions between rs10830962 and interventions were found: in women homozygous for the G allele but not in the other genotypes, the PA intervention reduced maternal fasting insulin (β: –0.16; 95% CI: –0.33, 0.02; P = 0.08) and HOMA-IR (β: –0.17; 95% CI: –0.35, 0.01; P = 0.06), and reduced cord blood leptin (β: –0.84; 95% CI: –1.42, –0.25; P = 0.01) and C-peptide (β: –0.62; 95% CI: –1.07, –0.17; P = 0.01). In heterozygous women, the HE intervention had no effect, whereas in women homozygous for the C allele, HE intervention reduced GWG (β: −1.6 kg; 95% CI: −2.4, −0.8 kg). No interactions were found.

          Conclusions

          In women homozygous for the risk allele of MTNR1B rs10830962, GDM risk was increased and PA intervention might be more beneficial than HE intervention for reducing maternal insulin resistance, cord blood C-peptide, and cord blood leptin.

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          Most cited references39

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          Variants in MTNR1B influence fasting glucose levels.

          To identify previously unknown genetic loci associated with fasting glucose concentrations, we examined the leading association signals in ten genome-wide association scans involving a total of 36,610 individuals of European descent. Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten studies. The strongest signal was observed at rs10830963, where each G allele (frequency 0.30 in HapMap CEU) was associated with an increase of 0.07 (95% CI = 0.06-0.08) mmol/l in fasting glucose levels (P = 3.2 x 10(-50)) and reduced beta-cell function as measured by homeostasis model assessment (HOMA-B, P = 1.1 x 10(-15)). The same allele was associated with an increased risk of type 2 diabetes (odds ratio = 1.09 (1.05-1.12), per G allele P = 3.3 x 10(-7)) in a meta-analysis of 13 case-control studies totaling 18,236 cases and 64,453 controls. Our analyses also confirm previous associations of fasting glucose with variants at the G6PC2 (rs560887, P = 1.1 x 10(-57)) and GCK (rs4607517, P = 1.0 x 10(-25)) loci.
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            Association of Gestational Diabetes With Maternal Disorders of Glucose Metabolism and Childhood Adiposity

            The sequelae of gestational diabetes (GD) by contemporary criteria that diagnose approximately twice as many women as previously used criteria are unclear.
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              Is Open Access

              A Genome-Wide Association Study of Gestational Diabetes Mellitus in Korean Women

              Knowledge regarding the genetic risk loci for gestational diabetes mellitus (GDM) is still limited. In this study, we performed a two-stage genome-wide association analysis in Korean women. In the stage 1 genome scan, 468 women with GDM and 1,242 nondiabetic control women were compared using 2.19 million genotyped or imputed markers. We selected 11 loci for further genotyping in stage 2 samples of 931 case and 783 control subjects. The joint effect of stage 1 plus stage 2 studies was analyzed by meta-analysis. We also investigated the effect of known type 2 diabetes variants in GDM. Two loci known to be associated with type 2 diabetes had a genome-wide significant association with GDM in the joint analysis. rs7754840, a variant in CDKAL1, had the strongest association with GDM (odds ratio 1.518; P = 6.65 × 10−16). A variant near MTNR1B, rs10830962, was also significantly associated with the risk of GDM (1.454; P = 2.49 × 10−13). We found that there is an excess of association between known type 2 diabetes variants and GDM above what is expected under the null hypothesis. In conclusion, we have confirmed that genetic variants in CDKAL1 and near MTNR1B are strongly associated with GDM in Korean women. There seems to be a shared genetic basis between GDM and type 2 diabetes.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                The American Journal of Clinical Nutrition
                Oxford University Press (OUP)
                0002-9165
                1938-3207
                February 2022
                February 09 2022
                December 04 2021
                February 2022
                February 09 2022
                December 04 2021
                : 115
                : 2
                : 388-396
                Affiliations
                [1 ]Institute of Human Movement Science, Sport and Health, University of Graz, Graz, Austria
                [2 ]Institut de Recerca de l´Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
                [3 ]CIBER Bioengineering, Biomaterials and Nanotechnology, Instituto de Salud Carlos III, Madrid, Spain
                [4 ]Recherche en Santé Lawson SA, Bronschhofen, Switzerland
                [5 ]Lawson Health Research Institute, London, Ontario, Canada
                [6 ]Western Sydney University, Campbelltown, New South Wales, Australia
                [7 ]Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, United Kingdom
                [8 ]Patia Europe, San Sebastian, Spain
                [9 ]Department of Obstetrics and Gynecology, Medical University Graz, Graz, Austria
                Article
                10.1093/ajcn/nqab347
                34669935
                59d98d6f-a78e-434a-aeac-11429f010943
                © 2021

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