Poulsen Asbjørn Seenithamby, Stisen Zara Rebecca, Skougaard Marie, Christensen Robin, Overgaard Anders, Gudbergsen Henrik, Jacobsen Stine, Balslev-Clausen Andreas Peter, Henriksen Marius, Kristensen Lars Erik, Bliddal Henning
The Parker Institute, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Denmark.
Department of Clinical Medicine, University of Copenhagen, Denmark.
Osteoarthr Cartil Open. 2025 Jan 3;7(1):100562. doi: 10.1016/j.ocarto.2024.100562. eCollection 2025 Mar.
Obesity is a major risk factor for osteoarthritis (OA). Adipose tissues may be linked to OA development through secretion of potential proinflammatory cytokines including neutrophil gelatinase-associated lipocalin (NGAL). Our objective was to assess changes in serum NGAL after a low-calorie diet (LCD) and subsequent glucagon-like peptide 1 receptor agonist (GLP-1 RA) treatment.
A secondary analysis of a randomized, double-blinded, placebo-controlled trial in adults with overweight (BMI≥27 kg/m) and symptomatic, early-to-moderate radiographic knee OA. Prior to randomization, participants underwent an 8-week LCD (week -8 to 0). Participants who lost min. 5 % of initial bodyweight were randomized 1:1 to liraglutide 3 mg/d or placebo for 52 weeks. Main outcome was change in serum NGAL from enrollment (week -8) to randomization (week 0). Other outcome was change in serum NGAL from week 0 to week 52 comparing liraglutide and placebo.
168 participants were enrolled to the initial intensive diet intervention; 127 participants, with NGAL samples, were randomized. Following the 8-week diet intervention, NGAL concentrations rose by 93.0 ng/mL (95 % CI: 18.9 to 167.1, = 0.015), with no correlation to weight loss magnitude. 52 weeks of treatment with either liraglutide or placebo, liraglutide did not cause a greater decrease in serum NGAL (14.9 ng/ml, 95%CI: -92.1 to 121.7 ng/mL, = 0.78).
An intensive 8-week calorie restriction was associated with a rise in serum NGAL. Compared to placebo, 52 weeks of liraglutide did not cause additional changes in NGAL. This indicates a complex pattern of proinflammatory cytokine-release during hypocaloric diet interventions.
Clinicaltrials.gov: NCT02905864.
肥胖是骨关节炎(OA)的主要危险因素。脂肪组织可能通过分泌包括中性粒细胞明胶酶相关脂质运载蛋白(NGAL)在内的潜在促炎细胞因子与OA的发展相关联。我们的目的是评估低热量饮食(LCD)及随后的胰高血糖素样肽1受体激动剂(GLP-1 RA)治疗后血清NGAL的变化。
对超重(BMI≥27 kg/m)且有症状的早中期放射学膝关节OA的成年人进行的一项随机、双盲、安慰剂对照试验的二次分析。在随机分组前,参与者接受为期8周的LCD(第-8周到0周)。体重减轻至少初始体重5%的参与者按1:1随机分为接受3 mg/d利拉鲁肽或安慰剂治疗52周。主要结局是从入组(第-8周)到随机分组(第0周)血清NGAL的变化。其他结局是比较利拉鲁肽和安慰剂从第0周到第52周血清NGAL的变化。
168名参与者参加了最初的强化饮食干预;127名有NGAL样本的参与者被随机分组。经过8周的饮食干预,NGAL浓度上升了93.0 ng/mL(95%CI:18.9至167.1,P = 0.015),与体重减轻幅度无关。利拉鲁肽或安慰剂治疗52周后,利拉鲁肽并未使血清NGAL有更大程度的降低(14.9 ng/ml,95%CI:-92.1至121.7 ng/mL,P = 0.78)。
为期8周的强化热量限制与血清NGAL升高有关。与安慰剂相比,52周的利拉鲁肽治疗并未使NGAL发生额外变化。这表明在低热量饮食干预期间促炎细胞因子释放模式复杂。
Clinicaltrials.gov:NCT02905864。