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54. Effects of prenatal exposure to the 1944–45 Dutch famine and glucocorticoid receptor polymorphisms on later life PTSD susceptibility

Author

Gultig, Kayleigh D., de Rooij, Susanne R., Hilberdink, Charlotte E., Olff, Miranda, Roseboom, Tessa J., and van Zuiden, Mirjam

Abstract

Background: Exposure to adversity in utero is thought to increase susceptibility to develop posttraumatic stress disorder (PTSD) following later life trauma, due to neurobiological programming effects during critical developmental periods. It remains unknown whether effects of prenatal adversity on PTSD susceptibility are modulated by genetic variations in neurobiological pathways implicated in PTSD susceptibility. Objective: We investigated whether genetic variation in the glucocorticoid receptor (GR) modulated effects of prenatal famine exposure on late adulthood PTSD symptom severity after trauma exposure in childhood and mid-to-late adulthood. Method: We included N = 439 term-born singleton adults (mean age: 72 years, 54.2% women) from the Dutch Famine Birth Cohort, born around the time of the Dutch Famine of 1944/1945, divided into exposure and control groups based on timing of the famine during gestation. Participants filled out self-report questionnaires on childhood (Childhood Trauma Questionnaire) and mid-to-late adulthood (Life Events Checklist for DSM-5) trauma, and current PTSD symptom severity (PTSD Checklist for DSM-5). GR haplotypes were determined from four functional GR single nucleotide polymorphisms (ER22/23EK, N363S, BclI and exon 9β) in previously collected DNA. Linear regression analyses were performed to investigate associations of GR haplotype and prenatal famine exposure in conjunction with later life trauma on PTSD symptom severity. Results: We observed a significant three-way interaction between the GR Bcll haplotype, famine exposure during early gestation, and adulthood trauma exposure on PTSD symptom severity in late adulthood. Only participants exposed to famine during early gestation without the GR Bcll haplotype showed a significantly stronger positive association between adulthood trauma and PTSD symptom severity than non-exposed participants, indicating increased PTSD susceptibility. Conclusions: Our results illustrate the importance of integrated approaches considering genetics and environmental contexts throughout various life periods, including the rarely investigated prenatal environment, to elucidate how PTSD susceptibility evolves throughout life. HIGHLIGHTSAdversity during pregnancy is thought to increase offspring’s PTSD risk following later life trauma, but exact neurobiological mechanisms underlying this process remain unknown.We found that effects of prenatal famine exposure on PTSD symptom severity were influenced by genetic variation in the glucocorticoid receptor, which signals effects of the stress hormone cortisol.Integrated approaches considering genetics and environmental contexts throughout both early and later life are important to understand how PTSD risk evolves throughout life. Adversity during pregnancy is thought to increase offspring’s PTSD risk following later life trauma, but exact neurobiological mechanisms underlying this process remain unknown. We found that effects of prenatal famine exposure on PTSD symptom severity were influenced by genetic variation in the glucocorticoid receptor, which signals effects of the stress hormone cortisol. Integrated approaches considering genetics and environmental contexts throughout both early and later life are important to understand how PTSD risk evolves throughout life.

Published
2023
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59. Long-term outcomes following antenatal exposure to low-dose aspirin: study protocol for the 4-year follow-up of the APRIL randomised controlled trial

Author

Landman, Anadeijda J E M C, Van limburg stirum, Emilie V J, Van 't hooft, Janneke, Leemhuis, Aleid G, Finken, Martijn J J, Van baar, Anneloes L, Roseboom, Tessa J, Ravelli, Anita C J, Van wely, Madelon, Oosterlaan, Jaap, Painter, Rebecca C, Pajkrt, Eva, Oudijk, Martijn A, De boer, Marjon A, Leerstoel Baar, Development and Treatment of Psychosocial Problems, Graduate School, Obstetrics and Gynaecology, Neonatology, Other Research, Epidemiology and Data Science, APH - Aging & Later Life, APH - Health Behaviors & Chronic Diseases, Amsterdam Reproduction & Development (AR&D), Medical Informatics, APH - Methodology, Center for Reproductive Medicine, APH - Personalized Medicine, General Paediatrics, APH - Quality of Care, Paediatrics, Obstetrics and gynaecology, Pediatrics, Amsterdam Gastroenterology Endocrinology Metabolism, Leerstoel Baar, and Development and Treatment of Psychosocial Problems

Subjects
Medicine(all), Aspirin, Tumor Necrosis Factor Ligand Superfamily Member 13, Infant, Newborn, PAEDIATRICS, General Medicine, Fetal medicine, Maternal medicine, PERINATOLOGY, Pregnancy, Child, Preschool, Humans, Premature Birth, EPIDEMIOLOGY, Female, Child, Follow-Up Studies, Randomized Controlled Trials as Topic
Abstract

IntroductionThe use of low-dose aspirin by pregnant women to prevent preterm pre-eclampsia is gradually increasing. The administration of aspirin during pregnancy improves perinatal outcome, which could translate into improved child outcome in the long term. However, antenatal exposure to aspirin could have adverse effects on child development that may manifest later in life. The aim of this follow-up study is to assess the long-term effects of antenatal exposure to low-dose aspirin compared with placebo on survival, (neuro)development, behaviour and general health at 4 years corrected age.Methods and analysisThis is a follow-up study of the Dutch double-blind randomised controlled APRIL trial which assessed the effectiveness of treatment with aspirin (80 mg daily) compared with placebo for the prevention of preterm birth in women with a previous spontaneous preterm birth. Treatment was initiated before 16 weeks of gestation and continued until 36 weeks or birth. We aim to follow-up all 379 children born to women who participated in the APRIL trial and survived the neonatal period, at the corrected age of 4 years. The main outcomes are (neuro)development as assessed by the Ages and Stages Questionnaire, and behaviour as assessed by the Strength and Difficulties Questionnaire. Additional outcomes include mortality, growth and general health from birth up to 4 years, and a composite outcome including mortality, abnormal (neuro)development and problem behaviour. Analyses will be performed by intention-to-treat using a superiority design.Ethics and disseminationInstitutional Review Board approval was obtained from the Medical Research Ethics Committee from Amsterdam Medical Center (no. W20 289#20.325). The results will be published in a peer-reviewed journal and presented at conferences.Trial registration numberThe APRIL trial (NTR5675, NL5553; EudraCT number 2015-003220-31) and the APRIL follow-up study (NL8950) are registered in the Dutch trial register. The study is funded by the Amsterdam Reproduction & Development research institute.

Published
2022
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60. Sex-dependence and comorbidities of the early-life adversity induced mental and metabolic disease risks: where are we at?

Author

Reemst, Kitty, Ruigrok, Silvie R., Bleker, Laura, Naninck, Eva F.G., Ernst, Tiffany, Kotah, Janssen M., Lucassen, Paul J., Roseboom, Tessa J., Pollux, Bart J.A., de Rooij, Susanne R., Korosi, Aniko, Structural and Functional Plasticity of the nervous system (SILS, FNWI), Epidemiology and Data Science, Obstetrics and Gynaecology, APH - Aging & Later Life, APH - Health Behaviors & Chronic Diseases, ARD - Amsterdam Reproduction and Development, and Paediatrics

Subjects
Male, Cognitive Neuroscience, Metabolic health, Placenta, Rodentia, Comorbidity, Maternal milk, Comorbidities, Behavioral Neuroscience, Metabolic Diseases, Adverse Childhood Experiences, Pregnancy, Risk Factors, Animals, Humans, Experimental Zoology, Rodent, Sex-differences, Early-life adversity, Neuropsychology and Physiological Psychology, Experimentele Zoologie, WIAS, Female, Mental health, Human
Abstract

Early-life adversity (ELA) is a major risk factor for developing later-life mental and metabolic disorders. However, if and to what extent ELA contributes to the comorbidity and sex-dependent prevalence/presentation of these disorders remains unclear. We here comprehensively review and integrate human and rodent ELA (pre- and postnatal) studies examining mental or metabolic health in both sexes and discuss the role of the placenta and maternal milk, key in transferring maternal effects to the offspring. We conclude that ELA impacts mental and metabolic health with sex-specific presentations that depend on timing of exposure, and that human and rodent studies largely converge in their findings. ELA is more often reported to impact cognitive and externalizing domains in males, internalizing behaviors in both sexes and concerning the metabolic dimension, adiposity in females and insulin sensitivity in males. Thus, ELA seems to be involved in the origin of the comorbidity and sex-specific prevalence/presentation of some of the most common disorders in our society. Therefore, ELA-induced disease states deserve specific preventive and intervention strategies.

Published
2022

65. Long-term outcomes following antenatal exposure to low-dose aspirin: study protocol for the 4-year follow-up of the APRIL randomised controlled trial

Author

Leerstoel Baar, Development and Treatment of Psychosocial Problems, Landman, Anadeijda J E M C, Van limburg stirum, Emilie V J, Van 't hooft, Janneke, Leemhuis, Aleid G, Finken, Martijn J J, Van baar, Anneloes L, Roseboom, Tessa J, Ravelli, Anita C J, Van wely, Madelon, Oosterlaan, Jaap, Painter, Rebecca C, Pajkrt, Eva, Oudijk, Martijn A, De boer, Marjon A, Leerstoel Baar, Development and Treatment of Psychosocial Problems, Landman, Anadeijda J E M C, Van limburg stirum, Emilie V J, Van 't hooft, Janneke, Leemhuis, Aleid G, Finken, Martijn J J, Van baar, Anneloes L, Roseboom, Tessa J, Ravelli, Anita C J, Van wely, Madelon, Oosterlaan, Jaap, Painter, Rebecca C, Pajkrt, Eva, Oudijk, Martijn A, and De boer, Marjon A

Published
2022

66. Development of a core outcome set for school-based intervention studies on preventing childhood overweight and obesity:study protocol

Author

De Vries, Lotte W., Harrington, Deirdre, Grooten, Iris, Van 'T Hooft, Janneke, Deutekom, Arend Van, Roseboom, Tessa J., Salmon, Jo, Chinapaw, Mai, Altenburg, Teatske M., De Vries, Lotte W., Harrington, Deirdre, Grooten, Iris, Van 'T Hooft, Janneke, Deutekom, Arend Van, Roseboom, Tessa J., Salmon, Jo, Chinapaw, Mai, and Altenburg, Teatske M.

Abstract

Introduction Prevention of childhood overweight is an important health priority. Evidence synthesis from studies evaluating school-based overweight preventive interventions is hampered by the wealth of different outcomes across studies. Therefore, consensus on a core set of outcomes for school-based overweight prevention studies is needed. This paper presents the protocol for the development of a core outcome set (COS) for school-based intervention studies aimed at childhood overweight prevention. Methods and analysis First, a scoping review will be performed to identify outcomes included in studies evaluating school-based overweight prevention interventions in 6-12 year-old children. Additionally, child focus groups will be organised in three countries to list the outcomes children consider important in school-based interventions. Next, an expert panel will identify all unique outcomes (eg, body composition) from the results of the scoping review and focus groups, ruling out how outcomes were defined and measured (eg, body mass index, body fat). In the next phase, a group of international stakeholders will participate in a Delphi study in which they will rate all unique outcomes on a 9-point Likert scale over three rounds to reach consensus on a COS. Participants will include healthcare professionals, policymakers, teachers, school leaders and parents of 6-12 year-olds. All rated outcomes will be presented to stakeholders in two online consensus meetings. Ethics and dissemination The Medical Ethics Committee of the VU Medical Center approved the child focus group study in the Netherlands (nr. 2020.071) and the Delphi study-including the consensus meeting (nr. 2022.0295). Other sites will obtain ethics approval for focus groups in their country. The University of Strathclyde School of Psychological Sciences ethics committee approved the Delphi study-including consensus meeting (nr. 72.27.04.2022.A). The final COS will be disseminated through the diverse networks

Published
2022

67. Which factors play a role in the decision of mothers to participate in child follow-up examinations after participation in an RCT?:a semi-quantitative study

Author

den Harink, Tamara, Hoek, Annemieke, Groen, Henk, Roseboom, Tessa J., Deutekom, Arend van, den Harink, Tamara, Hoek, Annemieke, Groen, Henk, Roseboom, Tessa J., and Deutekom, Arend van

Abstract

OBJECTIVES: To determine which factors contribute to the decision of mothers to participate with their child in follow-up (FU) examinations after participation in a randomised controlled trial (RCT) prior to conception. DESIGN: A cross-sectional survey, including Likert-scale items. Comparisons will be made between respondents who participated in all FU rounds of data collection and those who did not participate in any FU round with their child. PARTICIPANTS: Women who participated in an RCT investigating the effect of a preconception lifestyle intervention (LIFEstyle study: Netherlands Trial Register: NTR1530) were invited to participate with their child in three FU data collections when the child had a mean age of 4.2 years, 4.6 years and 6.5 years, respectively. FU rounds included a health questionnaire, physical examination and cardiac assessment, successively. RESULTS: Sixty-seven respondents were included, of whom 7 (10%) did not participate in any FU round and 24 (36%) participated in all FU rounds. Women who participated with their child in all 3 FU data collection rounds felt more involved in the FU research (95.8%) and agreed more often that the FU was introduced well (91.7%) as compared with women that did not participate in any FU data collection round with their child (14.3% and 28.6%, respectively). Participants of FU rounds more often agreed that participation felt like a health check for their child as compared with non-participants. In addition, participants of the physical examination and cardiac assessment more often let their decision to participate depend fully on their child, as compared with non-participants (39.4% vs 17.7% and 52.5% vs 24%, respectively). CONCLUSIONS: To increase participation rates in future FU studies of children after maternal participation in an RCT, we suggest to involve women in the design of the FU study, to emphasise possible perceived benefits of participation and to encourage women to actively involve their child

Published
2022

68. Depression, anxiety, and post-traumatic stress disorder symptoms after hyperemesis gravidarum: a prospective cohort study

Author

Nijsten, Kelly, van der Minnen, Loïs M., Dean, Caitlin, Bais, Joke M.J., Ris-Stalpers, Carrie, van Eekelen, Rik, Bremer, Henk A., van der Ham, David P., Heidema, Wieteke M., Huisjes, Anjoke, Kleiverda, Gunilla, Kuppens, Simone M., van Laar, Judith O.E.H., Langenveld, Josje, van der Made, Flip, Papatsonis, Dimitri, Pelinck, Marie José, Pernet, Paula J., van Rheenen-Flach, Leonie, Rijnders, Robbert J., Scheepers, Hubertina C.J., Vogelvang, Tatjana, Mol, Ben W., Olff, Miranda, Roseboom, Tessa J., Koot, Marjette H., Grooten, Iris J., Painter, Rebecca C., Nijsten, Kelly, van der Minnen, Loïs M., Dean, Caitlin, Bais, Joke M.J., Ris-Stalpers, Carrie, van Eekelen, Rik, Bremer, Henk A., van der Ham, David P., Heidema, Wieteke M., Huisjes, Anjoke, Kleiverda, Gunilla, Kuppens, Simone M., van Laar, Judith O.E.H., Langenveld, Josje, van der Made, Flip, Papatsonis, Dimitri, Pelinck, Marie José, Pernet, Paula J., van Rheenen-Flach, Leonie, Rijnders, Robbert J., Scheepers, Hubertina C.J., Vogelvang, Tatjana, Mol, Ben W., Olff, Miranda, Roseboom, Tessa J., Koot, Marjette H., Grooten, Iris J., and Painter, Rebecca C.

Abstract

Objective: To determine the prevalence of depression, anxiety, and posttraumatic stress disorder (PTSD) years after hyperemesis gravidarum (HG) and its association with HG severity. Material and methods: This prospective cohort study consisted of a follow-up of 215 women admitted for HG, who were eligible to participate in a randomized controlled trial and either declined or agreed to be randomized between 2013 and 2016 in 19 hospitals in the Netherlands. Participants completed the Hospital Anxiety and Depression Scale (HADS) six weeks postpartum and during follow-up and the PTSD checklist for DSM-5 (PCL-5) during follow-up. An anxiety or depression score ≥8 is indicative of an anxiety or depression disorder and a PCL-5 ≥ 31 indicative of PTSD. Measures of HG severity were symptom severity (PUQE-24: Pregnancy Unique Quantification of Emesis), weight change, duration of admissions, readmissions, and admissions after the first trimester. Results: About 54/215 participants completed the HADS six weeks postpartum and 73/215 participants completed the follow-up questionnaire, on average 4.5 years later. Six weeks postpartum, 13 participants (24.1%) had an anxiety score ≥8 and 11 participants (20.4%) a depression score ≥8. During follow-up, 29 participants (39.7%) had an anxiety score ≥8, 20 participants (27.4%) a depression score ≥8, and 16 participants (21.9%) a PCL-5 ≥ 31. Multivariable logistic regression analysis showed that for every additional point of the mean PUQE-24 three weeks after inclusion, the likelihood of having an anxiety score ≥8 and PCL-5 ≥ 31 at follow-up increased with OR 1.41 (95% CI: 1.10;1.79) and OR 1.49 (95% CI: 1.06;2.10) respectively. Conclusion: Depression, anxiety, and PTSD symptoms are common years after HG occurred.

Published
2022

69. Maternal obesity in pregnancy and children's cardiac function and structure:A systematic review and meta-analysis of evidence from human studies

Author

Den Harink, Tamara, Roelofs, Manouck J.M., Limpens, Jacqueline, Painter, Rebecca C., Roseboom, Tessa J., Van Deutekom, Arend W., Den Harink, Tamara, Roelofs, Manouck J.M., Limpens, Jacqueline, Painter, Rebecca C., Roseboom, Tessa J., and Van Deutekom, Arend W.

Abstract

The prevalence of obesity is increasing worldwide. Experimental animal studies demonstrate that maternal obesity during pregnancy directly affects cardiac structure and function in their offspring, which could contribute to their increased cardiovascular disease (CVD) risk. Currently, a systematic overview of the available evidence regarding maternal obesity and alterations in cardiac structure and function in human offspring is lacking. We systematically searched the electronic databases Embase, MEDLINE and NARCIS from inception to June 29, 2022 including human studies comparing cardiac structure and function from fetal life onwards in offspring of women with and without obesity. The review protocol was registered with PROSPERO International Prospective Register of Systematic Reviews (identifier: CRD42019125071). Risk of bias was assessed using a modified Newcastle-Ottawa scale. Results were expressed using standardized mean differences (SMD). The search yielded 1589 unique publications, of which thirteen articles were included. Compared to offspring of women without obesity, fetuses of women with obesity had lower left ventricular strain, indicative of reduced systolic function, that persisted in infancy (SMD -2.4, 95% confidence interval (CI) -4.4 standard deviation (SD) to -0.4 SD during fetal life and SMD -1.0, 95% CI -1.6 SD to -0.3 SD in infancy). Furthermore, infants born to women with obesity had a thicker interventricular septum (SMD 0.6 SD, 95% CI 0.0 to 1.2 SD) than children born to women without obesity. In conclusion, cardiac structure and function differs between fetuses and children of women with and without obesity. Some of these differences were present in fetal life, persisted in childhood and are consistent with increased CVD risk. Long-term follow-up research is warranted, as studies in offspring of older age are lacking.

Published
2022

70. Mediterranean-style diet in pregnant women with metabolic risk factors (ESTEEM): A pragmatic multicentre randomised trial

Author

H. Al Wattar, Bassel, Dodds, Julie, Placzek, Anna, Beresford, Lee, Spyreli, Eleni, Moore, Amanda, Gonzalez Carreras, Francisco J., Austin, Frances, Murugesu, Nilaani, Roseboom, Tessa J., Bes-Rastrollo, Maira, Hitman, Graham A., Hooper, Richard, Khan, Khalid S., and Thangaratinam, Shakila

Subjects
Metabolic diseases -- Risk factors -- Demographic aspects, Mediterranean diet -- Health aspects, Pregnancy complications -- Risk factors, Pregnant women -- Food and nutrition -- Health aspects, Stillbirth, Hypertension, Biological markers, Preeclampsia, Newborn infants, Gestational diabetes, Legumes, Beverages, Meat, Obesity, Olive oil, Vegetables, Diet, Fruits (Food), Biological sciences
Abstract

Background Pregnant women with metabolic risk factors are at high risk of complications. We aimed to assess whether a Mediterranean-style diet reduces adverse pregnancy outcomes in high-risk women. Methods and findings We conducted a multicentre randomised trial in 5 maternity units (4 in London and 1 in Birmingham) between 12 September 2014 and 29 February 2016. We randomised inner-city pregnant women with metabolic risk factors (obesity, chronic hypertension, or hypertriglyceridaemia) to a Mediterranean-style diet with high intake of nuts, extra virgin olive oil, fruits, vegetables, nonrefined grains, and legumes; moderate to high consumption of fish; low to moderate intake of poultry and dairy products; low intake of red and processed meat; and avoidance of sugary drinks, fast food, and food rich in animal fat versus usual care. Participants received individualised dietary advice at 18, 20, and 28 weeks' gestation. The primary endpoints were composite maternal (gestational diabetes or preeclampsia) and composite offspring (stillbirth, small for gestational age, or admission to neonatal care unit) outcomes prioritised by a Delphi survey. We used an intention-to-treat (ITT) analysis with multivariable models and identified the stratification variables and prognostic factors a priori. We screened 7,950 and randomised 1,252 women. Baseline data were available for 593 women in the intervention (93.3% follow-up, 553/593) and 612 in the control (95.6% follow-up, 585/612) groups. Over a quarter of randomised women were primigravida (330/1,205; 27%), 60% (729/1,205) were of Black or Asian ethnicity, and 69% (836/1,205) were obese. Women in the intervention arm consumed more nuts (70.1% versus 22.9%; adjusted odds ratio [aOR] 6.8, 95% confidence interval [CI] 4.3-10.6, p [less than or equal to] 0.001) and extra virgin olive oil (93.2% versus 49.0%; aOR 32.2, 95% CI 16.0-64.6, p [less than or equal to] 0.001) than controls; increased their intake of fish (p < 0.001), white meat (p < 0.001), and pulses (p = 0.05); and reduced their intake of red meat (p < 0.001), butter, margarine, and cream (p < 0.001). There was no significant reduction in the composite maternal (22.8% versus 28.6%; aOR 0.76, 95% CI 0.56-1.03, p = 0.08) or composite offspring (17.3% versus 20.9%; aOR 0.79, 95% CI 0.58-1.08, p = 0.14) outcomes. There was an apparent reduction in the odds of gestational diabetes by 35% (aOR 0.65, 95% CI 0.47-0.91, p = 0.01) but not in other individual components of the composite outcomes. Mothers gained less gestational weight (mean 6.8 versus 8.3 kg; adjusted difference -1.2 Kg, 95% CI -2.2 to -0.2, p = 0.03) with intervention versus control. There was no difference in any of the other maternal and offspring complications between both groups. When we pooled findings from the Effect of Simple, Targeted Diet in Pregnant Women With Metabolic Risk Factors on Pregnancy Outcomes (ESTEEM) trial with similar trials using random effects meta-analysis, we observed a significant reduction in gestational diabetes (odds ratio [OR] 0.67, 95% CI 0.53-0.84, I.sup.2 = 0%), with no heterogeneity (2 trials, 2,397 women). The study's limitations include the use of participant reported tools for adherence to the intervention instead of objective biomarkers. Conclusions A simple, individualised, Mediterranean-style diet in pregnancy did not reduce the overall risk of adverse maternal and offspring complications but has the potential to reduce gestational weight gain and the risk of gestational diabetes. Trial registration ClinicalTrials.gov NCT02218931., Author(s): Bassel H. Al Wattar 1,2, Julie Dodds 1, Anna Placzek 1, Lee Beresford 3, Eleni Spyreli 1, Amanda Moore 4, Francisco J. Gonzalez Carreras 1, Frances Austin 5, Nilaani [...]

Published
2019
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73. Survival effects of prenatal famine exposure

Author

van Abeelen, Annet FM, Veenendaal, Marjolein VE, Painter, Rebecca C, de Rooij, Susanne R, Dijkgraaf, Marcel GW, Bossuyt, Patrick MM, Elias, Sjoerd G, Grobbee, Diederick E, Uiterwaal, Cuno SPM, and Roseboom, Tessa J

Published
2012
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75. Depression, anxiety, and post-traumatic stress disorder symptoms after hyperemesis gravidarum: a prospective cohort study

Author

Nijsten, Kelly, primary, van der Minnen, Loïs M., additional, Dean, Caitlin, additional, Bais, Joke M. J., additional, Ris-Stalpers, Carrie, additional, van Eekelen, Rik, additional, Bremer, Henk A., additional, van der Ham, David P., additional, Heidema, Wieteke M., additional, Huisjes, Anjoke, additional, Kleiverda, Gunilla, additional, Kuppens, Simone M., additional, van Laar, Judith O. E. H., additional, Langenveld, Josje, additional, van der Made, Flip, additional, Papatsonis, Dimitri, additional, Pelinck, Marie-José, additional, Pernet, Paula J., additional, van Rheenen-Flach, Leonie, additional, Rijnders, Robbert J., additional, Scheepers, Hubertina C. J., additional, Vogelvang, Tatjana, additional, Mol, Ben W., additional, Olff, Miranda, additional, Roseboom, Tessa J., additional, Koot, Marjette H., additional, Grooten, Iris J., additional, and Painter, Rebecca C., additional

Published
2022
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76. Gelijk goed beginnen

Author

Roseboom, Tessa J., Epidemiology and Data Science, Amsterdam Reproduction & Development (AR&D), APH - Health Behaviors & Chronic Diseases, and APH - Aging & Later Life

Published
2022

77. Shaping the risk for late-life neurodegenerative disease: A systematic review on prenatal risk factors for Alzheimer’s disease-related volumetric brain biomarkers

Author

Boots, A, Wiegersma, A.M., Vali , Y, van den Hof, M, Langendam, Miranda W., Limpens, Juul, Backhouse, EV, Shenkin, Susan Deborah, Wardlaw, Joanna M., Roseboom, Tessa J., and de Rooij, Susanne R.

Subjects
Behavioral Neuroscience, Neuropsychology and Physiological Psychology, Brain reserve, Cognitive Neuroscience, Systematic review, Alzheimer's disease, Developmental programming, MRI
Abstract

Environmental exposures including toxins and nutrition may hamper the developing brain in utero, limiting the brain's reserve capacity and increasing the risk for Alzheimer's disease (AD). The purpose of this systematic review is to summarize all currently available evidence for the association between prenatal exposures and AD-related volumetric brain biomarkers. We systematically searched MEDLINE and Embase for studies in humans reporting on associations between prenatal exposure(s) and AD-related volumetric brain biomarkers, including whole brain volume (WBV), hippocampal volume (HV) and/or temporal lobe volume (TLV) measured with structural magnetic resonance imaging (PROSPERO; CRD42020169317). Risk of bias was assessed using the Newcastle Ottawa Scale. We identified 79 eligible studies (search date: August 30th, 2020; Ntotal=24,784; median age 10.7 years) reporting on WBV (N = 38), HV (N = 63) and/or TLV (N = 5) in exposure categories alcohol (N = 30), smoking (N = 7), illicit drugs (N = 14), mental health problems (N = 7), diet (N = 8), disease, treatment and physiology (N = 10), infections (N = 6) and environmental exposures (N = 3). Overall risk of bias was low. Prenatal exposure to alcohol, opioids, cocaine, nutrient shortage, placental dysfunction and maternal anemia was associated with smaller brain volumes. We conclude that the prenatal environment is important in shaping the risk for late-life neurodegenerative disease.

Published
2023
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81. Hyperemesis gravidarum severity, enteral tube feeding and cardiometabolic markers in offspring cord blood

Author

Nijsten, Kelly, primary, Koot, Marjette H., additional, Bais, Joke M. J., additional, Ris-Stalpers, Carrie, additional, van Eekelen, Rik, additional, Bremer, Henk A., additional, van der Ham, David P., additional, Heidema, Wieteke M., additional, Huisjes, Anjoke, additional, Kleiverda, Gunilla, additional, Kruizenga, Hinke, additional, Kuppens, Simone M., additional, van Laar, Judith O. E. H., additional, Langenveld, Josje, additional, van der Made, Flip, additional, Papatsonis, Dimitri, additional, Pelinck, Marie-José, additional, Pernet, Paula J., additional, van Rheenen-Flach, Leonie, additional, Rijnders, Robbert J., additional, Scheepers, Hubertina C. J., additional, Vogelvang, Tatjana, additional, Mol, Ben W., additional, Grooten, Iris J., additional, Roseboom, Tessa J., additional, and Painter, Rebecca C., additional

Published
2022
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94. Early life predictors of late life cerebral small vessel disease in four prospective cohort studies

Author

Backhouse, Ellen V, primary, Shenkin, Susan D, additional, McIntosh, Andrew M, additional, Bastin, Mark E, additional, Whalley, Heather C, additional, Valdez Hernandez, Maria, additional, Muñoz Maniega, Susana, additional, Harris, Mathew A, additional, Stolicyn, Aleks, additional, Campbell, Archie, additional, Steele, Douglas, additional, Waiter, Gordon D, additional, Sandu, Anca-Larisa, additional, Waymont, Jennifer M J, additional, Murray, Alison D, additional, Cox, Simon R, additional, de Rooij, Susanne R, additional, Roseboom, Tessa J, additional, and Wardlaw, Joanna M, additional

Published
2021
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95. Effectiveness of a 6-Month Lifestyle Intervention on Diet, Physical Activity, Quality of Life, and Markers of Cardiometabolic Health in Women with PCOS and Obesity and Non-PCOS Obese Controls: One Size Fits All?

Author

Wang, Zheng, primary, Groen, Henk, additional, Cantineau, Astrid E. P., additional, van Elten, Tessa M., additional, Karsten, Matty D. A., additional, van Oers, Anne M., additional, Mol, Ben W. J., additional, Roseboom, Tessa J., additional, and Hoek, Annemieke, additional

Published
2021
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96. The Effect of Lifestyle Intervention on Systemic Oxidative Stress in Women with Obesity and Infertility: A Post-Hoc Analysis of a Randomized Controlled Trial

Author

Wang, Zheng, primary, Bourgonje, Arno R., additional, Groen, Henk, additional, Abdulle, Amaal E., additional, Cantineau, Astrid E. P., additional, van Oers, Anne M., additional, van Dammen, Lotte, additional, Bulthuis, Marian L. C., additional, Wekker, Vincent, additional, Mol, Ben W. J., additional, Roseboom, Tessa J., additional, van Goor, Harry, additional, and Hoek, Annemieke, additional

Published
2021
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97. Long-term follow-up of children exposed in-utero to progesterone treatment for prevention of preterm birth: study protocol of the AMPHIA follow-up

Author

Simons, Noor E, primary, van Limburg Stirum, Emilie V J, additional, van Wassenaer-Leemhuis, Aleid G, additional, Finken, Martijn J J, additional, Aarnoudse-Moens, Cornelieke S H, additional, Oosterlaan, Jaap, additional, van Baar, Anneloes, additional, Roseboom, Tessa J, additional, Lim, Arianne C, additional, van Wely, Madelon, additional, de Boer, Marjon A, additional, Painter, Rebecca C, additional, Pajkrt, Eva, additional, Oudijk, Martijn A, additional, and van t Hooft, Janneke, additional

Published
2021
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99. Long-term follow-up of children exposed in-utero to progesterone treatment for prevention of preterm birth: study protocol of the AMPHIA follow-up

Author

Leerstoel Baar, Development and Treatment of Psychosocial Problems, Leerstoel Bogt, Simons, Noor E, Van Limburg Stirum, Emilie V J, Van Wassenaer-leemhuis, Aleid G, Finken, Martijn J J, Aarnoudse-moens, Cornelieke S H, Oosterlaan, Jaap, Van Baar, Anneloes, Roseboom, Tessa J, Lim, Arianne C, Van Wely, Madelon, De Boer, Marjon A, Painter, Rebecca C, Pajkrt, Eva, Oudijk, Martijn A, Van T Hooft, Janneke, Leerstoel Baar, Development and Treatment of Psychosocial Problems, Leerstoel Bogt, Simons, Noor E, Van Limburg Stirum, Emilie V J, Van Wassenaer-leemhuis, Aleid G, Finken, Martijn J J, Aarnoudse-moens, Cornelieke S H, Oosterlaan, Jaap, Van Baar, Anneloes, Roseboom, Tessa J, Lim, Arianne C, Van Wely, Madelon, De Boer, Marjon A, Painter, Rebecca C, Pajkrt, Eva, Oudijk, Martijn A, and Van T Hooft, Janneke

Published
2021

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