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Adipositas und die damit verbundenen Begleiterkrankungen zeigen einen deutlichen Anstieg der Prävalenz in der Bevölkerung. Auch für die Schwangerschaft gilt starkes Übergewicht als Risikofaktor für metabolische und vaskuläre Komplikationen wie Gestationsdiabetes mellitus (GDM) und Präeklampsie (PE). In den letzten 20 Jahren wurde eindrücklich nachgewiesen, dass eine Dysregulation von Fettzell-sezernierten Proteinen, sogenannten Adipokinen, ursächlich zu GDM und PE beitragen könnte. Zu Beginn der Dissertation lagen jedoch nur unzureichende Daten über die Regulation des Insulinresistenz-induzierenden, anti-adipogenen und anti-angiogenen Adipokins Preadipocyte factor-1 (Pref-1) bei GDM und PE vor. Die vorliegende Arbeit untersucht daher die Regulation von zirkulierendem Pref-1 bei GDM und PE sowie seine Expression in der Plazenta. Bei 74 Patientinnen mit GDM konnte kein signifikanter Unterschied der Pref-1 Konzentrationen (0.40 µg/l) verglichen zu 74 Gesunden (0.42 µg/l) (p = 0.655) festgestellt werden (Wurst U et al., Cytokine 2015; 71: 161–164). Es zeigte sich in der Kohorte eine unabhängige Assoziation zwischen Pref-1 und Schwangerschaftsalter bei der Blutentnahme, Triglyzeriden, Kreatinin, Body Mass Index und C reaktivem Protein (p < 0.05). In einer Studienkohorte von 51 Schwangeren mit PE wurden signifikant niedrigere Serumspiegel von Pref-1 (0.49 µg/l) im Vergleich zu 51 gesunden Schwangeren (0.68 µg/l) (p < 0.001) gemessen (Schrey S, Wurst U, et al., Cytokine 2015; 75: 338–343). In der multiplen Regressionsanalyse waren PE, Schwangerschaftsalter zum Zeitpunkt der Blutentnahme sowie zirkulierendes Leptin unabhängige Prädiktoren für Pref-1. Im peripartalen Zeitraum zeigte sich ein akuter und deutlicher Abfall von zirkulierendem Pref-1 im mütterlichen Blut und das Adipokin wurde immunhistochemisch im Plazentagewebe nachgewiesen. Die Daten dieser Studien sind vereinbar mit den Hypothesen, dass Pref-1 mit fortschreitender Schwangerschaft zunehmend produziert wird, die Plazenta zur Sekretion des Adipokins aktiv beiträgt sowie das Adipokin bei PE dysreguliert ist. Weiterführende Untersuchungen im Tiermodell sowie prospektive Studien sind notwendig, um die Signifikanz von Pref-1 bei GDM und PE näher zu untersuchen.

MicroRNA (miRNA) are short non-coding RNA molecules that regulate gene expression at the post-transcriptional level. Many miRNAs are involved in the pathogenesis of cardiovascular diseases, which is associated with altered gene expression. This work compares miRNA gene expression profiles among various biological sources - whole peripheral venous blood (whole PB), plasma and plasma exosomes. For all tested groups combined, the expression levels of miRNA were maximal in whole PB and lowered in plasma and plasma exosomes, and the expression levels of miRNA were higher in plasma than in plasma exosomes, except miR-126-3p, which had a higher level detected in plasma exosomes compared to plasma. This work also compares expression levels of cardiovascular miRNA between women with anamnesis of gestational diabetes mellitus (GDM) and physiological gravidity 3-11 years postpartum in whole PB, plasma and plasma exosomes. In whole PB, 12 of 29 tested miRNAs were up-regulated in women with prior exposure to GDM. MiR-181a-5p was up-regulated in plasma exosomes and miR-499a-5p in plasma in women with prior exposure to GDM. The changes in whole peripheral venous blood seem to reflect the complex systemic response to the changes that occurred during the onset of GDM. Women with aberrant epigenetic profiles may...

Gestational diabetes mellitus (GDM), a pregnancy-induced metabolic disorder that affects 2-10% of pregnancies poses future risk for diabetes mellitus (DM) and cardiovascular disease in mother and child. However, few prospective studies have examined the effect of GDM on altered maternal and cord blood lipids, specifically HDL, LDL, triglycerides, and total cholesterol, both during and after pregnancy. We have evaluated the association between GDM and lipid metabolism in pregnant mothers and their infants using data from a prospective cohort study conducted at Baystate Medical Center’s Wesson Women and Infant’s Unit. GDM was assessed prenatally by 3-hr GTT blood samples and was confirmed by obstetrician review. Lipids were assessed via fasting and non-fasting blood samples obtained during 3-hr GTTs performed at 24-28 weeks of gestation and 6-8 weeks post-partum. Data for covariates were collected via an interview form administered at the time of recruitment. We used multivariable linear regression to evaluate the association between GDM status and maternal lipids during and after pregnancy as well as cord lipids. These study results inform future research on GDM as a risk factor for future metabolic disorders in mother and child.

Aim:  The present study aimed to determine if foreign-born women from different countries of birth have a greater risk of GDM compared to Swedish-born women and to what extent income might mediate this relationship. Methods: This cross-sectional type study included 835279 women, of which 151,642 were foreign-born and 683637 were Swedish-born women who gave birth to their first singleton child in Sweden between 1997 to 2016. Register data from the Swedish Medical Birth Register, the Swedish Total Population Register, and the Longitudinal Integrated Database for Health Insurance and Labour Market Studies was used. Multiple Logistic Regression analysis and the Karlson-Holm-Breen methods were used to explore the relationship between GDM and country of birth and to estimate the proportion of the association explained by income. Results:  Foreign-born women demonstrated higher odds ratios for developing GDM than Swedish-born women. South East Asian women showed the highest risk of GDM (OR: 4.40, CI: 4.01-4.81) followed by Africa (OR: 3.42, CI: 3.07-3.81) and Middle East &amp; North Africa (OR: 2.92, CI: 2.67-3.20) respectively. Income partially explained the risk of GDM differences between foreign-born and Swedish-born women, accounting for 26% of the association. However, the proportion explained by income varies from 8.9% to 23.0% by country of birth. Conclusions:  A disparity exists in the risk of GDM based on country of birth, and Foreign-born women are more likely to have GDM and need additional support, including prenatal care and treatment. Since income only partially explains this association, other factors that may explain the association need to be explored.

Background: Although lifestyle modification is the cornerstone of GDM management, the evidence base on which dietary recommendations to prevent GDM is diverse and has not been synthesized in a consistent fashion. Objectives: The overall objective of this thesis is to assess the relationship of diet patterns, foods, and nutrients with GDM risk. Specifically, we seek to: 1) Quantify the relationship between dietary factors and GDM and metabolic disorders of pregnancy; 2) Compare the effects of dietary factors on markers of glycemic control, such as fasting glucose, fasting insulin, HbA1c, and the homeostatic model assessment for insulin resistance (HOMA-IR); 3) Assess the association and interaction between carbohydrate quality, and genetic load on the risk of developing GDM using data from 2 prospective birth cohort studies. Methods: We follow the approach set by the Cochrane Group’s Handbook for Systematic Review of Interventions to conduct meta-analyses and assess the quality of the evidence using the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach. We analyze prospective cohort data of 2,504 women from the CHILD and START studies, which enrolled women of White-Caucasian and South Asian ethnicity. We quantify carbohydrate quality by deriving the glycemic index and load (GL), and total and added sugar intake. We construct a gene score using 102 loci that were previously associated with type 2 diabetes in genome-wide association studies. Results: 1) The meta-analysis identified high-quality evidence that red meat increases GDM risk; however, most associations of foods and nutrients with GDM and other metabolic disorders of pregnancy are of low-quality; 2) The network meta-analysis identified that most dietary interventions given with gestational weight gain advice will lower fasting glucose; 3) In South Asians, a high GL coupled with a high genetic load increased GDM risk six fold, but a high total sugar intake in the presence of a high genetic load reduced GDM risk. This paradoxical finding may be explained by a high correlation between total sugars and other healthy foods. Conclusions: Few valid associations between dietary factors and GDM risk exist. GL and total sugars may modify the genetic risk of GDM in South Asians but not in White-Caucasians. Further research is needed to determine effective interventions that can assist women in adopting healthier eating habits during pregnancy. / Thesis / Doctor of Philosophy (PhD) / Gestational diabetes mellitus (GDM) is glucose intolerance that first appears during pregnancy. Although lifestyle modification is the cornerstone of GDM management, dietary recommendations for GDM prevention are sparse. The overarching objective of this thesis is to describe the relationships between diets, foods, and nutrients and GDM and metabolic disorders of pregnancy and to understand whether carbohydrate quality can modify a genetic predisposition to diabetes. In the systematic literature reviews, high-quality evidence showed that red meat increases GDM risk. Moderate-quality evidence showed that several dietary factors also influence the risk of GDM and metabolic disorders of pregnancy, but most of the existing evidence is of low-quality. More high-quality studies are needed before dietary interventions can be implemented In our genetic study, we observed that carbohydrate quality may modify the genetic risk of diabetes in South Asians but not in White-Caucasians and conclude that carbohydrate quality may provide only a limited assessment of overall diet quality.

O diabetes mellitus (DM) é definido como doença metabólica, caracterizado pela hiperglicemia, causada pela disfunção da secreção de insulina, atividade da insulina ou ambas. É classificado em quatro classes clínicas i) diabetes mellitus tipo 1 (DM1), ii) diabetes mellitus tipo 2 (DM2), iii) diabetes mellitus gestacional (DMG), iv) outros tipos específicos. Dentre os genes conhecidos por influenciarem o mecanismo de produção e liberação de insulina no organismo humano, o gene da insulina (INS) é o mais bem caracterizado nas classes clínicas do DM. A região promotora do gene INS tem sido alvo de estudo em diversas amostras populacionais do mundo, devido a sua capacidade de modular os níveis de expressão de insulina no timo e no pâncreas, de acordo, com a classe alélica que compõe o genótipo do indivíduo. Localizada a 596pb acima do sítio de transcrição do gene da insulina, é estruturada em alelos minissatélites distribuídos in tandem (ACAGGGGTGTGGGG). O alelo classe I (30 - 60 repetições) tem sido associado com predisposição ao DM1, enquanto o alelo classe III (120 - 170 repetições) tem efeito de proteção ao DM1, no entanto, esse alelo tem apresentado correlação ao DM2, à obesidade em crianças e jovens e, aumento de riscos cardiovasculares. O presente trabalho tem como objetivo analisar o polimorfismo da região promotora do gene da insulina sobre os fenótipos do DM e a possível influência desse em características demográficas, clínicas e laboratoriais desses pacientes. Foram analisados 189 pacientes com DM1, 116 pacientes com DM2, 68 pacientes com DMG e 339 indivíduos controle da região de Ribeirão Preto, SP. O DNA genômico foi extraído por salting-out, seguido da amplificação e digestão enzimática do fragmento referente a região promotora do gene INS, o qual contém na sequência downstream, o polimorfismo -23HphI, cujo desequilíbrio de ligação (r2 1) com o polimorfismo INSVNTR, permite inferir os genótipos por intermédio da análise do polimorfismo -23HphI. Observamos que o alelo classe I e o genótipo classe I : classe I estão relacionados à predisposição ao DM1, enquanto o alelo classe III, predominantemente em homozigose, está associado à proteção ao DM1. Em relação ao DM2, o genótipo classe I : classe III foi associado à susceptibilidade a doença e, nenhum genótipo foi correlacionado ao DMG. De acordo com os dados demográficos, clínicos e laboratoriais, variáveis como gênero e pigmentação da pele têm influenciado na frequência do polimorfismo INSVNTR em pacientes com DM1, como por exemplo, a maior frequência de homens com genótipo classe I : classe I no conjunto DM1. Em contrapartida, nesse mesmo grupo de pacientes, o genótipo classe III : classe III evidenciou maior susceptibilidade ao desenvolvimento de retinopatia (p=0,0020; OR= 0,05333; 95% I.C. 0,007839 - 0,3629). Em pacientes com DM2, a comparação entre gêneros evidenciou maior frequência do genótipo classe III : classe III em mulheres. E, em relação ao DMG, os genótipos de classe I : classe I e classe I : classe III estavam associados ao menor nível de glicose no plasma sanguíneo em relação as pacientes que exibiam o genótipo classe III : classe III. Esse é o primeiro estudo de associação do polimorfismo INS-VNTR comparando as três principais classes clínicas de DM oriundas de uma mesma amostra geográfica, sendo evidenciado um perfil genotípico padrão de susceptibilidade de acordo com o tipo de DM. / Diabetes mellitus (DM) is defined as a metabolic disorder characterized by hyperglycemia caused by impaired insulin secretion, insulin activity or both. It is classified into four clinical classes i) type 1 diabetes mellitus (T1DM), ii) type 2 diabetes mellitus (T2DM), iii) gestational diabetes mellitus (GDM), iv) other specific types. Among the genes known to influence the mechanism of production and release of insulin, the insulin gene (INS) has been well characterized in disease susceptibility. The INS promoter has been studied in different worldwide populations due to its ability to modulate expression levels of insulin in the thymus and pancreas, in accordance with the type of diabetes. The major polymorphic site is located 596bp upstream from the translation initiation site of the INS gene and it is structured into minisatellite alleles (ACAGGGGTGTGGGG). The shorter class I alleles (30 60 repeats) confers predisposition to DM1 and the longer class III (120 170 repeats) confers protection to DM1; however, the latter allele has also shown to be correlated with DM2, obesity in children and juvenile individuals, and increased cardiovascular risks. This study aims to analyze the association of a polymorphic site at promoter region of the INS gene with diabetes phenotypes, with the purpose of evaluating this region as a possible genetic marker of the disease, and the possible influence on demographic, clinical and laboratory features in a sample of the urban Brazilian population. We analyzed 189 T1DM patients, 116 T2DM patients, 68 GDM patients and 339 healthy individuals from the region of Ribeirão Preto, SP. DNA extraction was performed using a salting-out procedure, followed by amplification and restriction enzyme digestion of the fragment relating to INS gene promoter, which contains another polymorphism, -23HphI, which is in perfect linkage disequilibrium (r2 1) with the INS-VNTR, making it an useful genetic marker. We observed that the class I allele and class I : class I genotype are associated with predisposition to T1DM, whereas, class III allele, predominantly in homozygosity, is associated to T1DM protection. In relation to T2DM, the class I : class III genotype has been associated with susceptibility to disease. Finally, no genotype was correlated with GDM. Data stratification according to demographical, clinical and laboratory variables, indicated that gender, skin color seemed to influence the frequency of the INS-VNTR polymorphism; i. e., the class I : class I genotype was more frequent in male T1DM patients. On the other hand, the presence of the class III : class III genotype was associated with susceptibility the development of retinopathy (p=0,0020; OR= 0,05333; 95% I.C. 0,007839 - 0,3629). In T2DM patients, a trend association was observed between the class III : class III genotype with female diabetic patients. In relation to GDM, the genotypes class I : class I and class I : class III were associated with decreased glucose levels in relation to patients exhibiting the class III : class III genotype. This is the first study of the INS-VNTR polymorphism encompassing the major types if DM patients from the same geographical region, which showed a differential pattern of susceptibility according to the underlying type of DM.

O diabetes mellitus tipo 1 (DM1) tem etiologia autoimune, enquanto o diabetes mellitus tipo 2 (DM2) e o diabetes mellitus gestacional (DMG) são considerados como distúrbios metabólicos. Neste trabalho, foi realizada análise do transcriptoma das células mononucleares do sangue periférico (do inglês, peripheral mononuclear blood cells - PBMCs), obtidas de pacientes com DM1, DM2 e DMG, realizando análises por module maps a fim de comparar características patogênicas e aspectos gerais do tratamento com anotações disponíveis de genes modulados, tais como: a) análises disponíveis a partir de estudos de associação em larga escala (do inglês genome-wide association studies GWAS); b) genes associados ao diabetes em estudos clássicos de ligação disponíveis em bancos de dados públicos; c) perfis de expressão de células imunológicas fornecidos pelo grupo ImmGen (Immunological Project). Foram feitos microarrays do transcriptoma total da plataforma Agilent (Whole genome onecolor Agilent 4x44k) para 56 pacientes (19 DM1, 20 DM2 e 17 DMG). Para a compreensão dos resultados foram aplicados filtros não-informativos e as listas de genes diferencialmente expressos foram obtidas por análise de partição e análise estatística não-paramétrica (rank products), respectivamente. Posteriormente, análises de enriquecimento funcional foram feitas pelo DAVID e os module maps construídos usando a ferramenta Genomica. As análises funcionais contribuíram para discriminar os pacientes a partir de genes envolvidos na inflamação, em especial DM1 e DMG. Os module maps de genes diferencialmente expressos revelaram: a) genes modulados exibiram perfis de transcrição típicos de macrófagos e células dendríticas, b) genes modulados foram associados com genes previamente descritos como genes de complicação ao diabetes a partir de estudos de ligação e de meta-análises; c) a duração da doença, obesidade, número de gestações, níveis de glicose sérica e uso de medicações, tais como metformina, influenciaram a expressão gênica em pelo menos um tipo de diabetes. Esse é o primeiro estudo de module maps mostrando a influência de padrões epidemiológicos, clínicos, laboratoriais, imunopatogênicos e de tratamento na modulação dos perfis transcricionais em pacientes com os três tipos clássicos de diabetes: DM1, DM2 e DMG. / Type 1 diabetes (T1D) is an autoimmune disease while type 2 (T2D) and gestational diabetes (GDM) are considered as metabolic disturbances. We performed a transcriptome analysis of peripheral mononuclear blood cells obtained from T1D, T2D and GDM patients, and we took advantage of the module map approach to compare pathogenic and treatment features of our patient series with available annotation of modulated genes from i) genome-wide association studies; ii) genes provided by diabetes meta-analysis in public databases, iii) immune cell gene expression profiles provided by the ImmGen project. Whole genome one-color Agilent 4x44k microarray was performed for 56 (19 T1D, 20 T2D, 17 GDM) patients. Noninformative filtered and differentially expressed genes were obtained by partitioning and rank product analysis, respectively. Functional analyses were carried out using the DAVID software and module maps were constructed using the Genomica tool. Functional analyses contributed to discriminate patients on the basis of genes involved in inflammation, primarily for T1D and GDM. Module maps of differentially expressed genes revealed that: i) modulated genes exhibited transcription profiles typical of macrophage and dendritic cells, ii) modulated genes were associated with previously reported diabetes complication genes disclosed by association and meta-analysis studies, iii) disease duration, obesity, number of gestations, glucose serum levels and the use of medications, such as metformin, influenced gene expression profiles in at least one type of diabetes. This is the first module map study to show the influence of epidemiological, clinical, laboratory, immunopathogenic and treatment features on the modulation of the transcription profiles of T1D, T2D and GDM patients.

Introdução e objetivos – A finalidade prioritária no tratamento do diabetes mellitus gestacional (DMG) é alcançar níveis de glicemia materna tão próximos da normalidade quanto possível, a fim de reduzir os efeitos adversos associados à hiperglicemia na gestação. A auto verificação da glicemia capilar (perfil glicêmico) é o método mais usado para a monitorização do controle metabólico na gestação complicada por diabetes. Nosso objetivo foi analisar as associações entre os perfis glicêmicos maternos com os principais desfechos da gestação numa população de mulheres com DMG acompanhadas em ambulatório de pré-natal especializado em hospital universitário no sul do Brasil, Hospital de Clínicas de Porto Alegre (HCPA). Desenho e metodotologia – conduzimos um estudo de coorte prospectiva de gestantes referidas da rede de atenção primária de saúde pública para tratamento do DMG no HCPA, acompanhadas do diagnóstico ao parto. Pesquisamos associações entre os resultados dos perfis glicêmicos com o peso de nascimento e com o risco de recém-nascidos grandes para idade gestacional e de desfechos adversos perinatais. Resultados – acompanhamos 440 mulheres com DMG. A média do índice de massa corporal (IMC) foi 33.3kg/m2. 351 bebês (79.8%) mostraram peso adequado à idade gestacional no nascimento. As médias de glicemia nos perfis pré e pósprandiais aumentaram com o avanço na categoria de peso nascimento. Três ou mais perfis glicêmicos anormais foram o fator de risco mais robusto para o nascimento de bebês grandes (OR 3.15 1.51-6.55) e para o desenvolvimento de desfechos adversos perinatais (OR 2.28 1.59-3.29). O ganho de peso materno durante o tratamento associou-se ao risco de recém-nascido grande para idade gestacional, assim como o IMC pré-gestacional, esse último também fator de risco independente para eventos perinatais adversos. Conclusão – perfis glicêmicos anormais em mais de 2 ocasiões foram o fator de risco mais relacionado ao nascimento de um bebê grande para a idade gestacional e para o desenvolvimento de complicações neonatais. Efeito benéfico do tratamento do DMG, guiado pelos perfis glicêmicos, foi a maioria de recém-nascidos com peso adequado à idade gestacional nessa coorte, apesar da incidência de desfechos perinatais adversos não ter sido diferente entre as categorias de peso fetal de nascimento. / Background and objective – a priority target in the treatment of gestational diabetes mellitus (GDM) is attaining maternal glucose levels as close as possible to euglycemia, in order to decrease the adverse outcomes linked to hyperglycemia. Self-performed capillary glucose (glycemic profile) is the most widely used method for metabolic monitoring in pregnancy complicated by diabetes. We intended to analyze the associations of maternal glycemic profile to main pregnancy outcomes in a population of GDM women treated in a specialized prenatal clinic at a university hospital in South Brazil, Hospital de Clínicas de Porto Alegre (HCPA). Research design and methodology – we conducted a prospective cohort study of pregnant women, referred from public primary health care for treatment of GDM at HCPA, between 2008 and 2015. We searched associations of glycemic profiles to birth weight, large for gestational age newborn and adverse neonatal outcomes. Results – we followed 440 GDM women from diagnosis to delivery. Mean prepregnancy body mass index (BMI) was 33.3kg/m2; 351 babies (79.8%) had appropriate birth weight for gestational age. Mean glucose in pre-prandial and postprandial profiles increased with raising birth weight category. Three or more abnormal glycemic profiles showed the strongest association to a large baby (OR 3.15 1.51-6.55) and to a composite of adverse neonatal outcomes (OR 2.28 1.59- 3.29). Gestational weight gain in the course of treatment was associated to large babies, as pre-pregnancy BMI, the latter also an independent risk factor for adverse neonatal outcome. Conclusion – abnormal maternal glycemic profiles in more than two occasions were the stronger risk factor for delivering a large baby and for developing neonatal complications. A beneficial effect of GDM treatment, guided by glycemic profiles, was that most of our newborns had birth weight appropriate for gestational age, although incidence of adverse neonatal outcomes had been no different across birth weight categories.

Diss. (sammanfattning) Umeå : Umeå universitet, 2009. / Härtill 4 uppsatser. Även tryckt utgåva.