Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT04809571 |
Other study ID # |
2020/00079 |
Secondary ID |
|
Status |
Recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
February 22, 2021 |
Est. completion date |
January 31, 2024 |
Study information
Verified date |
September 2022 |
Source |
Institute of Bioengineering and Bioimaging (IBB) |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Inflammatory skin disorders are usually assessed by disease scoring system such as Scoring AD
(SCORAD)/Eczema Area and Severity Index (EASI) and Psoriasis Area and Severity Index (PASI)
for atopic eczema and psoriasis respectively. The current approach to score the severity of
these inflammatory skin disorders is through clinical observations and questionnaires. These
scores however do not reflect the structural characteristics of the skin such as morphology,
vasculature architecture and dermis thickness and are subject to inter and intra-assessor
variability. Objective inflammatory diseases indicators through non-invasive imaging
techniques have the potential to be an important clinical tool to shed light on its severity
in an objective manner. Furthermore, given the abundance of cutaneous vasculature,
non-invasive imaging in patients with chronic inflammatory skin conditions allows the
investigators to evaluate in detail how co-morbidities of metabolic syndrome, especially type
2 diabetes, further affects the vasculature or the epidermis in the skin. It helps to answer
the question of whether a tighter control of the "overlying" skin condition helps in
management of the underlying co-morbidities.
Currently, there are many skin imaging modalities available to visualize the morphology and
vascular architecture non-invasively, but they are hindered by their penetration depth and
lack of contrast. Examples include optical coherence tomography (OCT), high-frequency
ultrasound, and Doppler based ultrasound. In this study, these shortcomings will be
circumvented through the usage of photoacoustic mesoscopic imaging, a non-invasive, high
resolution, intrinsic or contrast-enhanced imaging technique, which can provide functional
and metabolic information at greater depths, and an optical fibre-based handheld confocal
Raman spectroscopy system with inbuilt data processing algorithms and software, which allows
for highly effective and accurate analysis of various skin constituents, such as ceramides,
filaggrin, and hydration. These technologies will allow the investigators to study
inflammatory and skin barrier markers in, as well as correlations between, psoriasis, eczema,
diabetes, and obesity. In addition, by studying the skin before and after therapeutic
interventions, this study will aid in understanding the mechanisms of action and efficacy of
various interventions.
Description:
Inflammatory skin diseases are increasingly common in various industrialized western
societies. In 2015, eczema or dermatitis, the most common inflammatory skin disease, is
estimated to have affected 245 million people worldwide. In fact, the biggest percentage of
cases seen in National Skin Centre (NSC), Singapore is for dermatitis (34.1%) while other
inflammatory skin diseases such as contact dermatitis and psoriasis account for 4.7% and 3.3%
of the cases respectively. Inflammatory skin diseases can cause remodeling of the
vasculature. This vascular remodeling is brought about by the imbalance between pro- and
anti-angiogenic mediators under conditions of chronic inflammation, resulting in either
vessel growth or recession. Vascular remodeling of affected skin usually display vascular
enlargement during inflammation. In psoriasis, for example, the skin capillaries expand and
become tortuous, making the lesions appear red due to the thinned epithelium.
Emerging evidence reports that chronic inflammatory skin diseases are closely related to
systemic complications such as atherosclerosis, type 2 diabetes or metabolic syndrome due to
systemic inflammation. One possible theory linking cutaneous and systemic vascular diseases
is from the release of products such as inflammatory cytokines produced in affected skin
lesions into the systemic circulation, resulting in the increased risk of inflammation in
other organs or tissues. It was reported that individuals with Atopic Dermatitis (AD) in the
adult US population tend to have a self-reported history of hypertension and adult-onset
diabetes even with control of body mass index and other comorbidities. An analysis of
different studies indicated that both individuals from Asia and North America with pediatric
and adult-onset of AD have a higher chance of being overweight, which can lead to other
metabolic diseases. It was also reported that there is an increased number of inflammatory
cells around vessels seen in histopathology biopsies of the human forearm skin for diabetic
patients compared to non-diabetic populations. The density of vascular network also tended to
be higher in diabetic patients in the forearms compared to non-diabetic subjects. However, no
difference in vascular networks were observed between subjects with Type 1 and Type 2
diabetes. The mechanism to explain the increased vessel density in diabetic subjects is not
known, though inflammation plays a role due to the presence of inflammatory cells. Since
inflammatory skin diseases are systemic disorders due to the co-morbidities, it would shed
light on the understanding of these diseases and their linkages to metabolic disease such as
diabetes.