VMP: Visualizing Vascular Mechanisms of Lipedema
Study Details
Study Description
Brief Summary
This work will address clinical unmet needs for patients with lipedema using advanced magnetic resonance imaging (MRI) methods, in sequence with portable clinical tools, by testing fundamental hypotheses regarding potential screening methods, lymphatic therapy, and vascular dysfunction in patients with lipedema.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Lipedema is a disease marked by disproportionate subcutaneous adipose tissue (SAT) accumulation in the lower extremities that is accompanied by somatic pain and edema (1). Importantly, lipedema is commonly misdiagnosed as obesity (2) and has been estimated to affect a high 11% of women (3). However, symptoms are refractory to diet, exercise, and other interventions for obesity (4) leading to a mean delayed diagnosis of 22 years, high physical morbidity (5), and lifelong distress (6). Despite growing awareness of lipedema as a distinct clinical entity, and a recent call to action for lipedema research (7), fundamental gaps persist in knowledge regarding both disease mechanisms and treatment options for this debilitating disease.
Over the past four years, multi-disciplinary study from investigators in radiology, vascular medicine, and physical therapy has demonstrated that lipedema has distinct characteristics from obesity. Using whole-body fat-and-water MRI, lipedema is characterized by a 42% higher lower-extremity SAT deposition compared to BMI-matched females without lipedema (p<0.001) (8). Using noninvasive sodium MRI technologies, skin sodium is also elevated in patients with lipedema compared to controls (14.9±2.9 vs. 11.9±2.0 mmol/L, p=0.01) in the lower extremities (8), but not upper extremities (9). Importantly, skin sodium decreases following 6-weeks of lymphatic stimulation by complete decongestive therapy (CDT) in preliminary study of patients with lipedema. These tissue signatures are consistent with those of patients with known lymphatic insufficiencies (i.e., secondary lymphedema). Recent findings of elevated arterial perfusion (10) and inflammatory profiles (11) in lipedema raise significant questions about how blood and lymphatic circulation are involved in lipedema.
The critical barrier to interrogating these systems, and more broadly addressing clinical unmet needs for evidence-based therapies for patients with lipedema, is that noninvasive lymphatic imaging strategies are traditionally underdeveloped. To address this barrier, non-tracer based MR lymphangiography is capable of visualizing lymphatic dilation and stasis in unilateral lymphedema (12), and similar features of lymphatic insufficiency are observed in the lower extremities of patients with lipedema (13).
This study will apply these MRI tools together with standard clinical tools to test the following hypotheses:
Hypothesis 1A: Ultrasound can be used as an accessible alternative to MRI for measuring subcutaneous fat deposition to distinguish lipedema from obesity.
Hypothesis 1B: Ultrasound measurement of fat deposition together with bedside tools for measuring water deposition have improved ability than ultrasound alone for distinguishing lipedema from controls.
Hypothesis 2: Tissue sodium is reduced following CDT in the lower extremities, but not in the untreated upper extremities, of patients with lipedema consistent with improved patient-reported outcomes.
Hypothesis 3: Lymphatic flow velocity is reduced, while arterial blood flow is elevated, in the legs of patients with lipedema compared to controls.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Participants pre CDT Participants with lipedema Biologically Female Age range = 18-80 years BMI range = 18 to 40 kg/m2 BMI range = 18 to 40 kg/m2 |
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| Controls Participants without lipedema Biologically Female Age range = 18-80 years BMI range = 18 to 40 kg/m2 |
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| Participants post CDT Participants with lipedema Biologically Female Age range = 18-80 years BMI range = 18 to 40 kg/m2 BMI range = 18 to 40 kg/m2 |
Outcome Measures
Primary Outcome Measures
- Change in tissue sodium content: quantification of tissue sodium content in treated limbs following the completion of therapy [at baseline and approximately 6 weeks later]
Tissue sodium content (mmol/L) quantified by sodium MRI
- Change in lymphedema severity: quantification of lymphatic stasis in treated limbs following the completion of therapy [at baseline and approximately 6 weeks later]
Lymphatic stasis area (mm^2) quantified by MR lymphangiography
- Baseline tissue sodium content: quantification of tissue sodium in affected limbs [At baseline]
Tissue sodium content (mmol/L) quantified by sodium MRI
- Baseline lymphedema severity: quantification of lymphatic stasis in affected limbs [At baseline]
Lymphatic stasis area (mm^2) quantified by MR lymphangiography
- Change in limb extracellular water: quantification of limb extracellular water in treated limbs following the completion of therapy [at baseline and approximately 6 weeks later]
Limb extracellular water (Ohms) estimated by bioimpedance spectroscopy
- Change in skin water: quantification of skin water in treated limbs following the completion of therapy [at baseline and approximately 6 weeks later]
Skin water (percent) estimated by tissue dielectric probe
- Change in skin elasticity: quantification of skin elasticity in treated limbs following the completion of therapy [at baseline and approximately 6 weeks later]
Skin elasticity (Newtons) quantified by fibrometer
- Baseline limb extracellular water: quantification of limb extracellular water in affected limbs [At baseline]
Limb extracellular water (Ohms) estimated by bioimpedance spectroscopy
- Baseline skin water: quantification of skin water in affected limbs [At baseline]
Skin water (percent) estimated by tissue dielectric probe
- Baseline skin elasticity: quantification of skin elasticity in affected limbs [At baseline]
Skin elasticity (Newtons) quantified by fibrometer
Eligibility Criteria
Criteria
Inclusion Criteria:
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Participants with and without lipedema
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Biologically Female
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Age range = 18-80 years
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BMI range = 18 to 40 kg/m2
Exclusion Criteria:
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Primary lymphedema
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Contraindication to 3T MRI
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Pregnant
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Severe claustrophobia
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Inability to provide written, informed consent
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Active infection anywhere in the body, or open wound on the lower-extremities or at locations for measurement
Also excluded are subjects incapable of giving informed written consent:
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Subjects who have an inability to communicate with the researcher for any reason
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Subjects who are non-English speaking who cannot communicate through a translator, or if a translator is not available
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Subjects who cannot adhere to the experimental protocols for any reason
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Subjects who have limited mental ability to give informed consent due to mental disability, confusion, or psychiatric disorders
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Prisoners
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Vanderbilt University Medical Center | Nashville | Tennessee | United States | 37216 |
Sponsors and Collaborators
- Vanderbilt University Medical Center
- National Heart, Lung, and Blood Institute (NHLBI)
Investigators
- Principal Investigator: Rachelle Crescenzi, PhD, Vanderbilt Medical Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 210181
- 1R01HL157378-01