The Impact of Metabolic Status on Pain and Central Sensitization in Women With Lipedema: A Cross-Sectional Observational Study
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Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
- Кому может быть актуально
- Состояния в реестре: Central Sensitization, Lipedema, Pain, HOMA-IR. Базовые параметры: от 18 лет · Женщины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Turkey (Türkiye)
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
THE IMPACT OF METABOLIC STATUS ON PAIN AND CENTRAL SENSITIZATION IN WOMEN WITH LIPEDEMA: A CROSS-SECTIONAL OBSERVATIONAL STUDY
Обзор
The aim of this study is to evaluate the effect of metabolic markers (HOMA-IR, triglyceride/HDL ratio, HbA1c, waist and hip circumference measurements, BMI, etc.) on pain and central sensitization in patients diagnosed with lipedema. The primary objective is to investigate the association between metabolic markers and central sensitization. The secondary objective is to assess the relationship between metabolic markers and pain intensity, pain phenotype, and functional status.
Подробное описание
Lipedema is a chronic disorder observed in women, characterized by symmetrical accumulation of adipose tissue in the lower extremities, easy bruising, and marked tenderness or pain. In lipedema, pain is often spontaneous, increases with pressure, and does not always correlate with the amount of adipose tissue. This suggests that lipedema-related pain cannot be explained solely by peripheral mechanical factors.
Previous studies in patients with lipedema have demonstrated reduced pressure pain thresholds, bilateral and symmetrical hyperalgesia, and increased pain sensitivity extending beyond the areas of local adipose tissue involvement. These findings suggest that alterations in central pain processing mechanisms may occur in lipedema and that central sensitization may play a role. However, systematic studies specifically evaluating central sensitization in lipedema remain limited.
Although lipedema has long been considered a "metabolically protected" condition, recent studies have reported that insulin resistance, dyslipidemia, and components of metabolic syndrome are more frequently observed, particularly in lipedema cases accompanied by obesity. HOMA-IR, which is used to evaluate insulin resistance; the triglyceride/HDL ratio (TG/HDL), a marker of atherogenic dyslipidemia; and HbA1c, reflecting long-term glycemic load, are closely associated with chronic inflammation and metabolic dysfunction.
In the chronic pain literature, metabolic dysfunction has been shown to play an important role in the development of central sensitization and nociplastic pain, with obesity, insulin resistance, and dyslipidemia being associated with central pain amplification. However, to the best of our knowledge, no studies in lipedema have simultaneously evaluated the relationship between metabolic parameters, pain phenotype, and central sensitization.
The aim of this study is to evaluate the effects of metabolic markers (HOMA-IR, triglyceride/HDL ratio, HbA1c, waist and hip circumference measurements, BMI, etc.) on pain and central sensitization in patients diagnosed with lipedema. The primary objective is to investigate the association between metabolic markers and central sensitization. The secondary objective is to assess the relationship between metabolic markers and pain intensity, pain phenotype, and functional status.
Первичные конечные точки
- Central Sensitization Inventory (CSI) [Срок оценки: At baseline]
Вторичные конечные точки (7)
- Numeric Rating Scale (NRS) [Срок оценки: At baseline]
- Fatigue Severity Scale (FSS) [Срок оценки: At baseline]
- Neuropathic Pain Diagnostic Questionnaire (DN4) [Срок оценки: At baseline]
- Short Form-12 (SF-12) [Срок оценки: At baseline]
- Jenkins Sleep Scale (JSS) [Срок оценки: At baseline]
- Lower Extremity Functional Scale (LEFS) [Срок оценки: At baseline]
- International Physical Activity Questionnaire (IPAQ) [Срок оценки: At baseline]
Критерии участия
Критерии включения
- Being female and aged 18 years or older
- Having chronic pain persisting for at least 3 months
- Having sufficient cognitive ability to understand and respond to the assessment scales used in the study
- Voluntarily agreeing to participate in the study and providing written informed consent
Критерии исключения
- Presence of a history of malignancy, active infection, inflammatory rheumatic disease, or severe systemic disease
- History of known neurological disorders (e.g., stroke, multiple sclerosis, epilepsy)
- Diagnosis of severe psychiatric disorders (e.g., psychotic disorders, bipolar disorder)
- Pregnancy or breastfeeding
- Presence of cognitive impairment or communication difficulties that could affect the study results
- Diagnosed diabetes mellitus
- Active thyroid disease (uncontrolled hypothyroidism or hyperthyroidism)
- Cushing's syndrome or other significant endocrine disorders
- Use of antidiabetic medications
- Use of lipid-lowering therapy (e.g., statins, fibrates)
- Systemic glucocorticoid use within the past 3 months
- Use of medications that may significantly affect central pain mechanisms (e.g., high-dose opioids, antipsychotic drugs)
- History of major surgery or invasive treatment for pain within the past 3 months
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Модель наблюдения
- Когортное
Центры проведения
Turkey (Türkiye) · 1 центр
- Marmara University Faculty of Medicine Pendik Training and Research Hospital — Istanbul
Идентификаторы
NCT: NCT07468097 · 09.2026.26-0134