THE IMPACT OF METABOLIC STATUS ON PAIN AND CENTRAL SENSITIZATION IN WOMEN WITH LIPEDEMA: A CROSS-SECTIONAL OBSERVATIONAL STUDY
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 59
- 试验地点
- 1
- 主要终点
- Central Sensitization Inventory (CSI)
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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
研究组 & 干预措施
Female patients diagnosed with lipedema
Patients aged 18 years and older who are followed with a diagnosis of lipedema and who have undergone laboratory testing in which metabolic markers were evaluated within the last three months.
结局指标
主要结局
Central Sensitization Inventory (CSI)
时间窗: At baseline
The Central Sensitization Inventory is a self-report screening tool developed to assess the presence and severity of symptoms associated with central sensitization. The inventory evaluates symptoms reflecting sensitization in central nervous system pain-processing mechanisms, including widespread pain, fatigue, sleep disturbances, and cognitive complaints. The CSI consists of 25 items, each scored on a scale from 0 to 4, with a total score ranging from 0 to 100. A total score of 40 or higher is considered to be associated with a high likelihood of central sensitization.
次要结局
- Numeric Rating Scale (NRS)(At baseline)
- Fatigue Severity Scale (FSS)(At baseline)
- Neuropathic Pain Diagnostic Questionnaire (DN4)(At baseline)
- Short Form-12 (SF-12)(At baseline)
- Jenkins Sleep Scale (JSS)(At baseline)
- Lower Extremity Functional Scale (LEFS)(At baseline)
- International Physical Activity Questionnaire (IPAQ)(At baseline)