Gestational Diabetes
Conditions
Brief summary
The aim of this study is to utilise ultrasound, using an established method for detecting NAFLD, to determine whether the presence of NAFLD in women with GDM, detected during routine scanning, is a marker of deterioration in glycaemic status post-partum. We propose to assess the relationship between NAFLD and surrogates for insulin resistance as well as glycaemic status, insulin sensitivity and β-cell function, after delivery. The study is not seeking to compare the incidence of T2DM between those with and without NAFLD. This would require a longer follow-up and larger cohort size. Instead, it aims to quantify the degree of early deterioration of glycaemic status in these groups using insulin resistance markers. This is a clinically important issue as a greater level of insulin resistance would in itself trigger clinical intervention, including vigilant follow-up and empowerment for proactive healthy life style changes, which have been shown to prevent diabetes development .
Interventions
DIAGNOSTIC_TESTMRI scan
On attendance to antenatal clinic with confirmed diagnosis of gestational diabetes based on OGTT and following informed consent: Ultrasound scan: Those with positive OGTT results (i.e. GDM positive) will attend an appointment for an ultrasound scan, as per routine practice. These women will,at that appointment, be assessed for presence/absence of NAFLD as well as undergoing their routine foetal assessment. This is a simple addendum to the existing scan, taking no more than 5 minutes. Participants will have been informed during the consent process that the results (regarding the presence / absence of NAFLD) will be compared to MRI after delivery.
Sponsors
University Hospitals of North Midlands NHS Trust
Diabetes UK
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Aged 18 and over * Pregnant women diagnosed with GDM based on OGTT
Exclusion criteria
* Women with known type 1 or type 2 diabetes prior to pregnancy * Women with known history of liver disease including alcoholic liver disease * Women unable or unwilling to consent to be part of the study * Women with contraindication to MRI
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary outcome measure for the study will be the mean difference in values of the HOMA-IR (as a surrogate for insulin resistance) in those with NAFLD vs. those without NAFLD 6-12 weeks post partum | 6-12 weeks post partum | To determine whether the presence of NAFLD during pregnancy in women with gestational diabetes mellitus is a marker of worse metabolic profile (insulin resistance). |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of HbA1c and fasting glucose (standard markers of dysglycaemia) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of disposition index (marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of QUICKI (marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of insulin and nonesterified fatty acid levels (marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of fasting levels from a 4 point OGTT (marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of area-under-the-curve from 4 point OGTT (marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of ELF blood test results (advanced marker of insulin resistance) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of liver function tests (as part of the Fatty Liver Index) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of Body Mass Index (as part of the Fatty Liver Index) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of waist circumference (as part of the Fatty Liver Index) in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| Comparison of alcohol history in those with NAFLD vs. those without NAFLD at 6-12 weeks post partum | 6-12 weeks post partum |
| The presence of fat in the liver using a liver ultrasound scan at baseline and 6-12 weeks post partum. | 6-12 weeks post partum |
| MRI scan to confirm the presence of NAFLD at 6-12 weeks post partum. | 6-12 weeks post partum |
Countries
United Kingdom
Outcome results
None listed