Skip to menu Skip to content Skip to footer
Dr James Cuffe
Dr

James Cuffe

Email: 
Phone: 
+61 7 336 53180

Overview

Background

Dr Cuffe is a systems physiologist focused on understanding the complex changes to maternal physiology that occur during pregnancy and the impact of pregnancy dysfunction of programmed cardiovascular, metabolic and renal disease in offspring. Dr Cuffe has a particular focus on understanding the role of the placenta and its hormones in mediating both maternal and offspring disease. He is most recognised for his research investigating how maternal stress, thyroid dysfunction, hypoxia or altered nutrition affect placental development and program disease in the mother after pregnancy as well as her offspring. Dr Cuffe has an exceptional track record and is excited to take new honours and PhD students into his research laboratory.

Availability

Dr James Cuffe is:
Available for supervision

Qualifications

  • Bachelor of Science, The University of Queensland
  • Bachelor (Honours) of Science (Advanced), The University of Queensland
  • Doctor of Philosophy, The University of Queensland

Research interests

  • Placental regulation of pregnancy disorders

    The placenta modulates almost every aspect of human physiology during pregnancy and it is the least understood of all human organs. It is known that placental dysfunction contributes to gestational diabetes, preeclampsia, stillbirth, preterm birth and fetal growth restriction and yet the mechanisms responsible are largely unknown. Much of my work focuses on understanding what goes wrong in the placenta to cause such poor outcomes in pregnancy.

  • Understanding the impact of thyroid disorders on pregnancy outcomes

    Given that thyroid disorders impact 1 in 20 women, it is essential to understand the links between these disorders and poor outcomes in pregnancy. In particular, I want to understand how targeting novel factors may ensure a healthy start to life for babies born to women with a thyroid disorder

  • Effects of maternal adversity on offspring physiology

    I am interested in understanding how stress, hypoxia or other causes of adversity during pregnancy can impair placental function and induce fetal growth restriction. Given that fetal growth restriction is associated with a range of adult onset diseases, I explore the link between these maternal factors and offspring cardiovascular, metabolic, neurological and renal dysfunction.

  • Understanding the role of poorly understood nutrients in pregnancy health and fetal development

    We must obtain a large number of micronutrients in our diet to ensure optimal health. The requirements for many of these micronutrients increase in pregnancy as the placenta actively transports these nutrients to the baby where they are required for essential biological processes or to provide the building blocks of life. This can mean that micronutrient deficiencies can become problematic at a time that the human body is undergoing the most significant changes to its physiology that occur during its lifetime. My research focuses on understand the key biological roles of such micronutrients in pregnancy which may better inform nutrient requirements to ensure a healthy pregnancy. I am currently most interested in understanding the roles of selenium and vitamin B12 in pregnancy in relation to poor pregnancy outcomes and long term disease in offspring.

  • Understanding the impact of metformin on placental formation

    Metformin is frontline medication used for management of endocrine disorders such as diabetes mellitus and polycystic ovary syndrome. Furthermore, it is one of only two treatments used to manage gestational diabetes. Metformin is known to induce its effects by impacting multiple pathways however, how it impacts maternal and fetal physiology in pregnancy is largely unknown. I am currently looking at how metformin impacts placental development and if some of the benefits of this drug are due to changes in placental function.

Works

Search Professor James Cuffe’s works on UQ eSpace

103 works between 2008 and 2025

81 - 100 of 103 works

2016

Conference Publication

Maternal Dexamethasone Exposure in the Mouse Causes Sex Specific Alterations in the Pattern of Glucocorticoid Receptor Isoform Expression

Cuffe, James, Saif, Zarqa, Moritz, Karen and Clifton, Vicki (2016). Maternal Dexamethasone Exposure in the Mouse Causes Sex Specific Alterations in the Pattern of Glucocorticoid Receptor Isoform Expression. Meeting of the International-Federation-of-Placenta-Associations (IFPA) - Placenta-Back to the Basics, Portland OR United States, 13-16 September 2016. United Kingdom: Elsevier. doi: 10.1016/j.placenta.2016.06.186

Maternal Dexamethasone Exposure in the Mouse Causes Sex Specific Alterations in the Pattern of Glucocorticoid Receptor Isoform Expression

2016

Book Chapter

The developmental origins of renal dysfunction

Cuffe, James S. M., Walton, Sarah L. and Moritz, Karen M. (2016). The developmental origins of renal dysfunction. The epigenome and developmental origins of health and disease. (pp. 291-314) edited by Cheryl S. Rosenfeld. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-801383-0.00015-3

The developmental origins of renal dysfunction

2015

Journal Article

Maternal hypomagnesemia causes placental abnormalities and fetal and postnatal mortality

Schlegel, R. N., Cuffe, J. S. M., Moritz, K. M. and Paravicini, T. M. (2015). Maternal hypomagnesemia causes placental abnormalities and fetal and postnatal mortality. Placenta, 36 (7), 750-758. doi: 10.1016/j.placenta.2015.03.011

Maternal hypomagnesemia causes placental abnormalities and fetal and postnatal mortality

2015

Journal Article

Excess prenatal corticosterone exposure results in albuminuria, sex-specific hypotension and altered heart rate responses to restraint stress in aged adult mice

O'Sullivan, Lee, Cuffe, James S. M., Koning, Anselm, Singh, Reetu R., Paravicini, Tamara M. and Moritz, Karen M. (2015). Excess prenatal corticosterone exposure results in albuminuria, sex-specific hypotension and altered heart rate responses to restraint stress in aged adult mice. American Journal of Physiology: Renal Physiology, 308 (10), F1065-F1073. doi: 10.1152/ajprenal.00676.2014

Excess prenatal corticosterone exposure results in albuminuria, sex-specific hypotension and altered heart rate responses to restraint stress in aged adult mice

2015

Journal Article

Differential mRNA expression and glucocorticoid-mediated regulation of TRPM6 and TRPM7 in the heart and kidney throughout murine pregnancy and development

Cuffe, James S. M., Steane, Sarah, Moritz, Karen M. and Paravicini, Tamara M. (2015). Differential mRNA expression and glucocorticoid-mediated regulation of TRPM6 and TRPM7 in the heart and kidney throughout murine pregnancy and development. PLoS One, 10 (2) e0117978, e0117978. doi: 10.1371/journal.pone.0117978

Differential mRNA expression and glucocorticoid-mediated regulation of TRPM6 and TRPM7 in the heart and kidney throughout murine pregnancy and development

2015

Conference Publication

Maternal corticosterone exposure in the mouse causes sex specific alterations in placental OGT and O-linked glycosylation

Cuffe, James, Steane, Sarah, McMahon, Kathryn, Moritz, Karen and Pantaleon, Marie (2015). Maternal corticosterone exposure in the mouse causes sex specific alterations in placental OGT and O-linked glycosylation. International Federation of Placenta Associations Meeting, Brisbane, QLD Australia, 2015. London, United Kingdom: Elsevier. doi: 10.1016/j.placenta.2015.07.199

Maternal corticosterone exposure in the mouse causes sex specific alterations in placental OGT and O-linked glycosylation

2015

Conference Publication

Restraint stress induces distinct changes in redox status within the hippocampus and striatum accompanied by an up-regulation of protective antioxidant genes

Spiers, Jereme, Chen, Hsiao-Jou Cortina, Cuffe, James, Sernia, Conrad and Lavidis, Nickolas (2015). Restraint stress induces distinct changes in redox status within the hippocampus and striatum accompanied by an up-regulation of protective antioxidant genes. 45th Annual Meeting of the International-Society-of-Psychoneuroendocrinology (ISPNE) on Stress and the Brain - From Fertility to Senility, Edinburgh, Scotland, 08-11 September 2015. Kidlington, Oxford, United Kingdom: Pergamon Press. doi: 10.1016/j.psyneuen.2015.07.591

Restraint stress induces distinct changes in redox status within the hippocampus and striatum accompanied by an up-regulation of protective antioxidant genes

2015

Conference Publication

Placental Glycogen Deposition: a Cause or Consequence of Impaired Placental Development Contributing to Fetal Growth Restriction?

Moritz, Karen, Cuffe, James and Simmons, David (2015). Placental Glycogen Deposition: a Cause or Consequence of Impaired Placental Development Contributing to Fetal Growth Restriction?. International Federation of Placenta Associations Meeting, Brisbane, QLD Australia, 2015. London, United Kingdom: Elsevier. doi: 10.1016/j.placenta.2015.07.219

Placental Glycogen Deposition: a Cause or Consequence of Impaired Placental Development Contributing to Fetal Growth Restriction?

2014

Journal Article

The effects of gestational age and maternal hypoxia on the placental renin angiotensin system in the mouse

Cuffe, J. S. M., Walton, S. L., Steane, S. E., Singh, R. R., Simmons, D. G. and Moritz, K. M. (2014). The effects of gestational age and maternal hypoxia on the placental renin angiotensin system in the mouse. Placenta, 35 (11), 953-961. doi: 10.1016/j.placenta.2014.09.004

The effects of gestational age and maternal hypoxia on the placental renin angiotensin system in the mouse

2014

Journal Article

Mid- to late term hypoxia in the mouse alters placental morphology, glucocorticoid regulatory pathways and nutrient transporters in a sex-specific manner

Cuffe, J. S. M., Walton, S. L, Singh, R. R, Spiers, J. G., Bielefeldt-Ohmann, H., Wilkinson, L., Little, M. H. and Moritz, K. M. (2014). Mid- to late term hypoxia in the mouse alters placental morphology, glucocorticoid regulatory pathways and nutrient transporters in a sex-specific manner. The Journal of Physiology, 592 (14), 1-15. doi: 10.1113/jphysiol.2014.272856

Mid- to late term hypoxia in the mouse alters placental morphology, glucocorticoid regulatory pathways and nutrient transporters in a sex-specific manner

2014

Journal Article

Periconceptional alcohol consumption causes fetal growth restriction and increases glycogen accumulation in the late gestation rat placenta

Gardebjer E.M., Cuffe J.S.M., Pantaleon M., Wlodek M.E. and Moritz K.M. (2014). Periconceptional alcohol consumption causes fetal growth restriction and increases glycogen accumulation in the late gestation rat placenta. Placenta, 35 (1), 50-57. doi: 10.1016/j.placenta.2013.10.008

Periconceptional alcohol consumption causes fetal growth restriction and increases glycogen accumulation in the late gestation rat placenta

2013

Journal Article

The effects of low-moderate dose prenatal ethanol exposure on the fetal and postnatal rat lung

Probyn, M. E., Cuffe, J. S. M., Zanini, S. and Moritz, K. M. (2013). The effects of low-moderate dose prenatal ethanol exposure on the fetal and postnatal rat lung. Journal of Developmental Origins of Health and Disease, 4 (5), 358-367. doi: 10.1017/S2040174413000305

The effects of low-moderate dose prenatal ethanol exposure on the fetal and postnatal rat lung

2013

Journal Article

Prenatal exposure to Dexamethasone in the mouse alters cardiac growth patterns and increases pulse pressure in aged male offspring

O'Sullivan, Lee, Cuffe, James S. M., Paravicini, Tamara M., Campbell, Sally, Dickinson, Hayley, Singh, Reetu R., Gezmish, Oksan, Black, M. Jane and Moritz, Karen M. (2013). Prenatal exposure to Dexamethasone in the mouse alters cardiac growth patterns and increases pulse pressure in aged male offspring. PLoS One, 8 (7) e69149, e69149.1-e69149.11. doi: 10.1371/journal.pone.0069149

Prenatal exposure to Dexamethasone in the mouse alters cardiac growth patterns and increases pulse pressure in aged male offspring

2013

Conference Publication

Reduced Nephron Number But Hypotension in Male Mouse Offspring Following Prenatal Corticosterone Exposure

Singh, R., Koning, A., O'Sullivan, L., Cuffe, J., Paravicini, T. and Moritz, K. (2013). Reduced Nephron Number But Hypotension in Male Mouse Offspring Following Prenatal Corticosterone Exposure. 49th Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Brisbane, QLD Australia, 9-11 September 2013. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12121

Reduced Nephron Number But Hypotension in Male Mouse Offspring Following Prenatal Corticosterone Exposure

2012

Journal Article

Short and long term effects of exposure to natural and synthetic glucocorticoids during development

Singh, Reetu R., Cuffe, James S.M and Moritz, Karen M. (2012). Short and long term effects of exposure to natural and synthetic glucocorticoids during development. Clinical and Experimental Pharmacology and Physiology, 39 (11), 979-989. doi: 10.1111/1440-1681.12009

Short and long term effects of exposure to natural and synthetic glucocorticoids during development

2012

Journal Article

Maternal corticosterone exposure in the mouse has sex-specific effects on placental growth and mRNA expression

Cuffe, J. S. M., O'Sullivan, L., Simmons, D. S., Anderson, S. T. and Moritz, K. M. (2012). Maternal corticosterone exposure in the mouse has sex-specific effects on placental growth and mRNA expression. Endocrinology, 153 (11), 5500-5511. doi: 10.1210/en.2012-1479

Maternal corticosterone exposure in the mouse has sex-specific effects on placental growth and mRNA expression

2012

Other Outputs

The effects of maternal glucocorticoid exposure on the developing placenta

Cuffe, James Sebastian Martin (2012). The effects of maternal glucocorticoid exposure on the developing placenta. PhD Thesis, School of Biomedical Sciences, The University of Queensland.

The effects of maternal glucocorticoid exposure on the developing placenta

2011

Journal Article

Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse

Cuffe, J. S. M., Dickinson, H., Simmons, D. G. and Moritz, K. M. (2011). Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse. Placenta, 32 (12), 981-989. doi: 10.1016/j.placenta.2011.09.009

Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse

2011

Conference Publication

Glucocorticoid specific changes in fetal heart growth and alterations in FGF-2 following prenatal exposure in the mouse

O'Sullivan, Lee, Cuffe, James S. M., Campbell, Sally and Moritz, Karen M. (2011). Glucocorticoid specific changes in fetal heart growth and alterations in FGF-2 following prenatal exposure in the mouse. 7th World Congress on Developmental Origins of Health and Disease (DOHaD), Portland, Oregon, United States, 18–21 September 2011. Cambridge, England, U.K.: Cambridge University Press. doi: 10.1017/S204017441100047X

Glucocorticoid specific changes in fetal heart growth and alterations in FGF-2 following prenatal exposure in the mouse

2010

Journal Article

Review: Sex specific programming: A critical role for the renal renin-angiotensin system

Moritz, K. M., Cuffe, J. S M, Wilson, L. B., Dickinson, H., Wlodek, M. E., Simmons, D. G. and Denton, K. M. (2010). Review: Sex specific programming: A critical role for the renal renin-angiotensin system. Placenta, 31 (SUPPL.). doi: 10.1016/j.placenta.2010.01.006

Review: Sex specific programming: A critical role for the renal renin-angiotensin system

Funding

Past funding

  • 2023 - 2025
    Selenium supplementation: Can a simple nutritional supplement prevent fetal loss linked to thyroid autoimmunity?
    Allen Foundation Inc.
    Open grant
  • 2021 - 2023
    Do thyroid antibodies disrupt placental arterial remodelling in pregnancy
    American Thyroid Association
    Open grant
  • 2020 - 2022
    Understanding the relationship between vitamin B12 deficiency in pregnancy and Gestational Diabetes Mellitus
    Allen Foundation Inc.
    Open grant
  • 2019
    Advanced Brightfield and Fluorescent High Speed and Throughput Slide Scanner for biological, medical, materials science, and agricultural applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2019
    Vevo 3100 Imaging System for ultrahigh resolution and frame rate echocardiographic assessment of small animals.
    UQ Major Equipment and Infrastructure
    Open grant
  • 2012
    Placental clock gene expression in the Spiny Mouse
    UWA-UQ Bilateral Research Collaboration Award
    Open grant

Supervision

Availability

Dr James Cuffe is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • Investigating placental contributions to complications of pregnancy

    The placenta regulates all aspects of pregnancy health. It secretes factors into the maternal system to control maternal blood glucose concentrations, blood pressure and neurological function. This study will investigate key pathological processes in the placenta which may contribute to gestational diabetes, preeclampsia, preterm birth and intrauterine growth restriction.

  • Investigating how micro-nutrient deficiencies during pregnancy lead to metabolic and renal disease in offspring.

    Given that only 1 in 20 Australians consume the recommended dietary intake of fruit and vegetables, most Australians would be deficient in key micronutrients when they fall pregnant. Deficiencies in these micronutrients is known to increase maternal risk of gestational diabetes and preeclampsia but their influence on offspring physiology is less well understood. This study will investigate the role of specific micronutrients in fetal development and offspring physiology. Most particularly, this project will focus on diabetes and renal disease in offspring, two comorbid conditions known to be affected by events that occur before birth.

  • Investigating placental contributions to complications of pregnancy

    The placenta regulates all aspects of pregnancy health. It secretes a range of steroid, protein and peptide hormones into the maternal system to override normal homeostatic processes resulting in drastic physiological changes to almost all biological systems. Such changes result in a significant expansion of blood volume, cardiac hypertrophy, redistribution of metabolic resources, altered insulin production, insulin resistance as well changes to neurological function. This study will investigate how pathological processes in the placenta impact hormone secretion and this may contribute to miscarriage, stillbirth, gestational diabetes, preeclampsia, preterm birth and intrauterine growth restriction. This study also aims to increase our knowledge of poorly understood proteins that are only secreted by the placenta that likely have significant biological roles. To achieve these outcomes, this study will use a combination of clinical samples from pregnant people as well as targeted animal and in vitro models.

  • Investigating how thyroid autoimmunity impacts pregnancy outcomes: Possible role of selenium as a treatment

    Thyroid autoimmunity is the most common cause of thyroid dysfunction in areas that are iodine sufficient. Patients with thyroid autoimmunity have antibodies that target key thyroid proteins. These thyroid antibodies can disrupt thyroid function leading to thyroid disease. However, a large number of individuals have high levels of these antibodies without having yet developing changes to thyroid hormone levels. Approximately 1 in 6 pregnant people are positive for thyroid antibodies, and this increases their risk of a range of pregnancy complications, even if their thyroid hormone levels are within normal ranges. This study aims to investigate the biological processes by which thyroid antibodies lead to a range of pregnancy related disorders. For instance, we will investigate how thyroid antibodies impact vascular smooth muscle cell migration and how this might lead to preeclampsia or growth restriction. Currently, there are no suitable treatments for reducing thyroid antibody levels however, there is a large amount of emerging evidence that suggests that selenium supplementation might improve outcomes. Therefore this study will also explore how selenium can alter the biological processes shown to be impacted by thyroid antibodies.

Supervision history

Current supervision

  • Doctor Philosophy

    Investigating the effects of Autoimmune Thyroiditis on Pregnancy Physiology

    Principal Advisor

  • Doctor Philosophy

    Understanding the impact of metformin on one carbon metabolism, placental function and fetal outcomes.

    Principal Advisor

    Other advisors: Dr David Simmons

  • Doctor Philosophy

    Understanding the relationship between vitamin B12 deficiency in pregnancy and gestational diabetes mellitus

    Principal Advisor

    Other advisors: Associate Professor Karin Borges

  • Doctor Philosophy

    Treating thyroid autoimmunity in pregnancy with selenium supplementation

    Principal Advisor

    Other advisors: Associate Professor Karin Borges

  • Doctor Philosophy

    Investigating the effects of Autoimmune Thyroiditis on Pregnancy Physiology

    Principal Advisor

  • Doctor Philosophy

    Understanding the impact of metformin on one carbon metabolism, placental function and fetal outcomes.

    Principal Advisor

    Other advisors: Dr David Simmons

  • Doctor Philosophy

    A new the mechanism for the coexistence of hypercortisolaemia and inflammation: GRalpha D1

    Associate Advisor

  • Doctor Philosophy

    Glycogen in Epilepsy

    Associate Advisor

    Other advisors: Dr Nela Durisic, Associate Professor Karin Borges

Completed supervision

Media

Enquiries

For media enquiries about Dr James Cuffe's areas of expertise, story ideas and help finding experts, contact our Media team:

communications@uq.edu.au