Justiina Ronkainen

ORCID: 0000-0001-7375-8099
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About
Contact & Profiles
Research Areas
  • Birth, Development, and Health
  • Epigenetics and DNA Methylation
  • Gestational Diabetes Research and Management
  • Health, Environment, Cognitive Aging
  • Pregnancy and preeclampsia studies
  • Prenatal Substance Exposure Effects
  • Nutritional Studies and Diet
  • Obesity, Physical Activity, Diet
  • Neonatal Respiratory Health Research
  • Iron Metabolism and Disorders
  • Ovarian function and disorders
  • Renal Diseases and Glomerulopathies
  • Adipokines, Inflammation, and Metabolic Diseases
  • Telomeres, Telomerase, and Senescence
  • Cardiovascular Disease and Adiposity
  • Genetic Syndromes and Imprinting
  • RNA modifications and cancer
  • Adipose Tissue and Metabolism
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Hemoglobinopathies and Related Disorders
  • Peroxisome Proliferator-Activated Receptors
  • Diet and metabolism studies
  • Drug Transport and Resistance Mechanisms
  • RNA Research and Splicing
  • Histiocytic Disorders and Treatments

University of Oulu
2015-2025

The Kids Research Institute Australia
2022

The University of Western Australia
2022

Imperial College London
2022

Biocenter Finland
2020

Oulu University Hospital
2015-2016

Ageing is a biological and psychosocial process related to diseases mortality. It correlates with changes in DNA methylation (DNAm) all human tissues. Therefore, epigenetic markers can be used estimate age using DNAm profiling across tissues.We developed Bioconductor package that allows computation of several existing adult/childhood gestational clocks. Functions visualize the prediction versus chronological correlation between clocks are also available as well other features, such missing...

10.1093/bioinformatics/btaa825 article EN Bioinformatics 2020-09-08
Robin N. Beaumont Christopher Flatley Marc Vaudel Xiaoping Wu Jing Chen and 83 more Gunn-Helen Moen Line Skotte Øyvind Helgeland Pol Solé-Navais Karina Banasik Clara Albiñana Justiina Ronkainen João Fadista Sara Stinson Katerina Trajanoska Carol A. Wang David Westergaard Sundararajan Srinivasan Carlos Sánchez-Soriano José Ramón Bilbao Catherine Allard Marika Groleau Teemu Kuulasmaa Daniel J. Leirer Frédérique White Pierre‐Étienne Jacques Haoxiang Cheng Ke Hao Ole A. Andreassen Bjørn Olav Åsvold Mustafa Atalay Laxmi Bhatta Luigi Bouchard Ben Brumpton Søren Brunak Jonas Bybjerg‐Grauholm Cathrine Ebbing Paul Elliott Line Engelbrechtsen Christian Erikstrup Marisa Estarlich Paul W. Franks Romy Gaillard Frank Geller Jakob Grove David M. Hougaard Eero Kajantie Camilla S. Morgen Ellen A. Nøhr Mette Nyegaard Colin N. A. Palmer Ole Birger Pedersen Fernando Rivadeneira Sylvain Sebért Beverley M. Shields Camilla Stoltenberg Ida Surakka Lise Wegner Thørner Henrik Ullum Marja Vääräsmäki Bjarni J. Vilhjálmsson Cristen J. Willer Timo A. Lakka Dorte Jensen Gybel-Brask Mariona Bustamante Torben Hansen Ewan R. Pearson Rebecca M. Reynolds Sisse Rye Ostrowski Craig E. Pennell Vincent W. V. Jaddoe Janine F. Felix Andrew T. Hattersley Mads Melbye Debbie A. Lawlor Kristian Hveem Thomas Werge Henriette Svarre Nielsen Per Magnus David M. Evans Bo Jacobsson Marjo‐Riitta Järvelin Ge Zhang Marie‐France Hivert Stefan Johansson Rachel M. Freathy Bjarke Feenstra Pål R. Njølstad

Abstract A well-functioning placenta is essential for fetal and maternal health throughout pregnancy. Using placental weight as a proxy growth, we report genome-wide association analyses in the ( n = 65,405), 61,228) paternal 52,392) genomes, yielding 40 independent signals. Twenty-six signals are classified fetal, four three maternal. parent-of-origin effect seen near KCNQ1 . Genetic correlation colocalization reveal overlap with birth genetics, but 12 loci predominantly or only affecting...

10.1038/s41588-023-01520-w article EN cc-by Nature Genetics 2023-10-05

The Horizon2020 LifeCycle Project is a cross-cohort collaboration which brings together data from multiple birth cohorts across Europe and Australia to facilitate studies on the influence of early-life exposures later health outcomes. A major product this has been establishment FAIR (findable, accessible, interoperable reusable) resource known as EU Child Cohort Network. Here we focus Network's core variables. These are set basic variables, derivable by majority participating frequently used...

10.1007/s10654-021-00733-9 article EN cc-by European Journal of Epidemiology 2021-04-21

Abstract Common variants of human fat mass- and obesity-associated gene Fto have been linked with higher body mass index, but the biological explanation for link has remained obscure. Recent findings suggest that these affect homeobox protein IRX3. Here we report FTO a role in white adipose tissue which modifies its response to high-fat feeding. Wild type -deficient mice were exposed standard or diet 16 weeks after metabolism, behavior morphology analyzed together adipokine levels relative...

10.1038/srep09233 article EN cc-by Scientific Reports 2015-03-18

Children's biological age does not always correspond to their chronological age. In the case of BMI trajectories, this can appear as phase variation, which be seen shift, stretch, or shrinking between trajectories. With maturation thought a process moving towards final state - adult BMI, we assessed whether children divided into latent groups reflecting similar maturational BMI. The were characterised by early factors and time-related features We used data from two general population birth...

10.1038/s41366-025-01714-8 article EN cc-by International Journal of Obesity 2025-01-16

Genetic variants in the fat mass- and obesity-associated gene Fto are linked to onset of obesity humans. The causal role FTO protein is supported by evidence obtained from transgenic mice; however, underlying molecular pathways pertaining have yet be established. In this study, we investigate mouse brown adipose tissue browning process white tissue. We analyze distinct structural factors depots Fto-deficient mice under normal obesogenic conditions. report significant alterations morphology...

10.3390/ijms17111851 article EN International Journal of Molecular Sciences 2016-11-07

Aging | doi:10.18632/aging.203872. Anna Freni-Sterrantino, Giovanni Fiorito, Angelo D'Errico, Oliver Robinson, Marianna Virtanen, Leena Ala-Mursula, Marjo-Riitta Järvelin, Justiina Ronkainen, Paolo Vineis

10.18632/aging.203872 article IT cc-by Aging 2022-02-02

Abstract Higher birth order is associated with altered risk of many disease states. Changes in placentation and exposures to utero growth factors successive pregnancies may impact later life via persistent DNA methylation alterations. We investigated Illumina array data each 16 cohorts (8164 newborns) European, African, Latino ancestries from the Pregnancy Childhood Epigenetics Consortium. Meta-analyzed demonstrated systematic variation 341 CpGs (FDR adjusted P < 0.05) 1107 regions. Forty...

10.1038/s42003-023-05698-x article EN cc-by Communications Biology 2024-01-09

Objective and methods The impact of the rs9939609 FTO variant on cardiovascular events was investigated in 19-year follow-up subjects recruited to OPERA study.Results A total 212 disease (CVD) 152 coronary heart (CHD) or deaths occurred during follow-up. logistic regression analysis revealed that among AA genotype incidence CHD (OR 1.905; 95% CI 1.250–2.903, p = 0.001) CVD 1.849; 1.265–2.702, 0.003) death significantly higher when adjusted for age, sex, study group. After further adjustment...

10.3109/07853890.2015.1091088 article EN Annals of Medicine 2015-11-11

The current epidemics of cardiovascular and metabolic noncommunicable diseases have emerged alongside dramatic modifications in lifestyle living environments. These correspond to changes our "modern" postwar societies globally characterized by rural-to-urban migration, modernization agricultural practices, transportation, climate change, aging. Evidence suggests that these are related each other, although the social biological mechanisms as well their interactions yet be uncovered....

10.1097/ee9.0000000000000184 article EN cc-by-nc-nd Environmental Epidemiology 2021-12-28

Activation of pregnane X receptor (PXR) elevates circulating 4β-hydroxycholesterol (4βHC), an agonist liver (LXR). PXR may also regulate 25-hydroxycholesterol and 27-hydroxycholesterol. Our aim was to elucidate the roles oxysterols in regulation cholesterol transporters. We measured serum volunteers dosed with rifampicin 600 mg/day versus placebo for a week analysed expression transporters mononuclear cells. The effect 4βHC on transport studied human primary monocyte-derived macrophages foam...

10.3389/fphar.2020.00361 article EN cc-by Frontiers in Pharmacology 2020-03-27

Leucocyte telomere length (LTL) has been associated with nonalcoholic fatty liver disease (NAFLD), but the evidence is imperfect. Furthermore, fibrosis shown to correlate mortality and recent studies have also found associations LTL suggesting that may additional prognostic value in diseases. Our objective was study association of NAFLD evaluate prognosis subjects. Study subjects (n = 847) were middle-aged hypertensive patients. All participants evaluated for their measured at baseline....

10.1080/00365513.2022.2059698 article EN cc-by-nc-nd Scandinavian Journal of Clinical and Laboratory Investigation 2022-04-13

Abstract STUDY QUESTION Can a genome-wide association study (GWAS) meta-analysis, including large sample of young premenopausal women from founder population Northern Finland, identify novel genetic variants for circulating anti-Müllerian hormone (AMH) levels and provide insights into single-nucleotide polymorphism enrichment in different biological pathways tissues involved AMH regulation? SUMMARY ANSWER The meta-analysis identified total six loci associated with at P < 5 × 10−8,...

10.1093/humrep/deae117 article EN cc-by-nc Human Reproduction 2024-05-30

Abstract Background Globally, one in ten babies is born preterm (<37 weeks), and 1–2% at very low birth weight (VLBW, <1500 g). As adults, they are increased risk for a plethora of health conditions, e.g., cardiometabolic disease, which may partly be mediated by epigenetic regulation. We compared blood DNA methylation between young adults VLBW controls. Methods 157 subjects 161 controls term, from the Helsinki Study Very Low Birth Weight Adults, were assessed peripheral venous levels...

10.1038/s41390-024-03354-6 article EN cc-by Pediatric Research 2024-06-19

Abstract Idiopathic Pulmonary Fibrosis (IPF) is a rare disease with poor prognosis. By contrast, cancer common in any elderly population and leading killer, but now often curable. Of note, whereas IPF driven by cellular senescence, characterized uncontrolled cell division. Using data available from two large biobank-based studies (Finnish FinnGen study UK biobank), we conducted comprehensive analysis of the shared genetic background cancer. In sample 218,792 Finns complete longitudinal...

10.1101/2021.05.07.21255988 preprint EN cc-by-nd medRxiv (Cold Spring Harbor Laboratory) 2021-05-10

Abstract Objectives Type 2 diabetes (T2D) and comorbid depression challenges clinical management particularly in individuals with overweight. We aim to explore the shared etiology, via lifecourse adiposity, between T2D depression. Methods used data from birth until 46years Northern Finland Birth Cohort 1966 ( n = 6,372; 53.8% females). conducted multivariate analyses on three outcomes: (4.2%), (19.2%) as comorbidity (1.8%). (i) Path analysis clarify time-dependent body mass index (BMI)...

10.1038/s41366-022-01134-y article EN cc-by International Journal of Obesity 2022-05-13

Telomeres are DNA-protein complexes that protect chromosome ends from DNA damage and surrogate biomarkers of cellular aging. Current evidence, almost entirely cross-sectional observations, supports negative associations between leukocyte telomere length (LTL) adverse lifestyle factors cardiometabolic risk factors. Polycystic ovary syndrome (PCOS), the most common gynecological endocrine disorder, is associated with inflammation oxidative stress, both accelerated attrition. We therefore...

10.1530/eje-22-0462 article EN cc-by European Journal of Endocrinology 2022-09-08

Altered maternal haemoglobin levels during pregnancy are associated with pre-clinical and clinical conditions affecting the fetus. Evidence from animal models suggests that these associations may be partially explained by differential DNA methylation in newborn possible long-term consequences. To test this humans, we meta-analyzed epigenome-wide of offspring 3,967 cord blood 1,534 children 1,962 adolescent whole-blood samples derived 10 cohorts. was measured using Illumina Infinium...

10.1080/15592294.2020.1864171 article EN cc-by-nc-nd Epigenetics 2020-12-17

Understanding the biological mechanisms behind multimorbidity patterns in adolescence is important as they may act intermediary risk factor for long-term health. We aimed to explore relationship between prenatal exposures and adolescent's psycho-cardiometabolic traits mediated through epigenetic biomarkers, using structural equation modeling (SEM). used data from mother-child dyads pregnancy adolescents at 16-17 years two prospective cohorts: Northern Finland Birth Cohort 1986 (NFBC1986)...

10.1007/s00787-024-02390-1 article EN cc-by European Child & Adolescent Psychiatry 2024-02-17
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