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Non-alcoholic Fatty Liver Disease in Low Birth Weight Individuals

Increased Risk of Non-alcoholic Fatty Liver Disease in Low Birth Weight Individuals - Reversibility and Mechanistic Studies.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05842850
Enrollment
8
Registered
2023-05-06
Start date
2026-01-01
Completion date
2026-12-01
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NAFLD

Keywords

Adipose tissue biology, Caloric restriction, Insulin resistance, Energy expenditure, Insulin secretion

Brief summary

The investigators will conduct a proof-of-principle 4-weeks low-calorie diet (LCD) intervention study in low birth weight (LBW) subjects and normal birth weight (NBW) controls with documented (MR scan) liver fat content equal to or above 5%. The investigators will provide extended in-depth mechanistic insight into the role of impaired subcutaneous adipose tissue (SAT) expandability in ectopic fat deposition before and after LCD.

Detailed description

An adverse fetal environment characterized by low birth weight (LBW) plays a key role in the development of type 2 diabetes (T2D). The investigators recently demonstrated a 3-fold increase in liver fat in 26 early middle-aged LBW compared to 22 normal birth weight (NBW) men, and 20% of the LBW - but none of the normal birth weight (NBW) - men had previously unknown non-alcoholic fatty liver disease (NAFLD). The investigators hypothesize that ectopic fat deposition and NAFLD is among the earliest disease manifestations and on the critical path to the development of more severe cardiometabolic disease in LBW. The investigators furthermore hypothesize, that LBW individuals exhibit ectopic liver fat due to reduced capacity to store fat in the subcutaneous adipose tissue (SAT) depot, and that early detection and subsequent intensive caloric restriction, in middle-aged LBW individuals with overt NAFLD, may represent a targeted and highly efficient way forward to prevent more severe cardiometabolic disease manifestations in LBW subjects. To further explore the recent findings, the investigators aim to perform an extended nested case-control screening study for NAFLD (now MASLD) in 250 early middle-aged non-obese LBW men and women, and subsequently to conduct a proof-of-principle 4 week low-calorie diet (LCD) intervention study in the subjects with hepatic fat content of or above 5% (MR scan). Individuals identified with MALSD in the screening study will be invited to participate in the reversibility study. The reversibility study includes measures of hepatic fat content (primary outcome) MR, fibroscan, DEXA scan, clinical biochemistry and collection of SAT adipose tissue biopsies and progenitor cells for further studies before and after the LCD intervention. The investigators will provide extended in-depth mechanistic insight into transcriptional, epigenetic as well as functional SAT and preadipocyte perturbations underlying impaired SAT expandability in individuals with and without MASLD studied before and after different dietary interventions including LCD and high carbohydrate overfeeding.

Interventions

BEHAVIORALCaloric restriction intervention

The intervention consist of 4-weeks low calories diet (LCD) using total meal replacement from NUPO. A dietician will guide the participants an ensure well-being during the intervention.

OTHERNo intervention

No intervention

Sponsors

Steno Diabetes Center Copenhagen
Lead SponsorOTHER
Aarhus University Hospital
CollaboratorOTHER
Lund University
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants with MASLD will be recruited from a nested case-control (NAFLD) screening study. Participants will be examined at baseline and after 4-weeks low-calorie diet (LCD). Participants will be guided to a dietician ensuring overall week-being. Participant will be examined by MR and DEXA scans, Fibroscan, blood samples for clinical biochemistry including liver enzymes. A fasting subcutaneous adipose tissue (SAT) biopsy will be obtained and progenitor cell collected for later studies.

Eligibility

Sex/Gender
ALL
Age
35 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* subjects with NAFLD (liver fat content ≥5% liver fat content verified on MRS in the screening NAFLD study)

Exclusion criteria

* BMI\<18.5 and BMI\>30 kg/m2 * Family history of diabetes (siblings, parent, and grandparents) * Disease/medication known to affect primary outcome * Self-reported high physical activity level * Alcohol intake above general recommendations. * Metabolic/liver disease * Weight gain/loss of \>3 kg within the past 6 months

Design outcomes

Primary

MeasureTime frameDescription
Liver fat contentChange from baseline in liver fat content at 4 weeksValidation by Magnetic resonance spectroscopy (MRS)

Secondary

MeasureTime frameDescription
Liver stiffnessBaseline and after 4 weeksLiver elastography (FibroScan)
Body compositionBaseline and after 4 weeksDEXA scan

Countries

Denmark

Contacts

CONTACTCharlotte Brøns, PhD
charlotte.broens.01@regionh.dk+4526129093
PRINCIPAL_INVESTIGATORCharlotte Brøns, PhD

Steno Diabetes Center Copenhagen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 5, 2026