Habib Syed Shahid, Alkahtani Shaea, Alhussain Maha, Aljuhani Osama
Department of Physiology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Department of Exercise Physiology, College of Sport Sciences and Physical Activity, King Saud University, Riyadh, Saudi Arabia.
Diabetes Metab Syndr Obes. 2020 Aug 25;13:3089-3097. doi: 10.2147/DMSO.S260382. eCollection 2020.
The associations between sarcopenia, adiposity indices and metabolic dysregulation still remain controversial. We aimed to assess and compare insulin resistance and metabolic profile in sarcopenic and non-sarcopenic obese Saudi adult men.
This cross sectional study was conducted at the College of Sports Sciences, King Saud University, Riyadh. We recruited 312 Saudi adult male individuals and 288 were finally selected for the study. Body composition analysis and hand grip strength (HGS) were estimated by bioimpedance analysis (BIA) and dynamometer in all subjects, respectively. Fasting blood samples were collected for glucose (FBG), basal insulin (BI) and lipid profile. The subjects were divided into three groups based on the body composition parameters, appendicular lean mass (ALM) and body fat percentage (BF%), into non-obese (NonOb) [Normal ALM+<25 BF%], obese without sarcopenia (ObNonS) [Normal ALM+>25 BF%] and obese with sarcopenia (ObS) [Low ALM+>25 BF%].
Obese subjects had significantly higher BI, HOMA-IR and HOMA-β compared to non-obese. Moreover, comparison between two obese groups revealed that both BI and HOMA-IR levels were higher in ObS subjects compared to ObNonS individuals revealing that sarcopenia exacerbates the insulin resistance profile. There was a significant trend of higher resistance and lower sensitivity from non-obese to obesity with sarcopenia. Total cholesterol (TC) and triglycerides (TG) were significantly higher and high density lipoprotein cholesterol (HDL-C) was significantly lower in sarcopenic obese subjects compared to non-sarcopenic obese individuals. The worsening effects were more significant at cutoff point of 7.46 on insulin indices and lipid profile showing that sarcopenia associated with obesity exacerbates the dyslipidemia.
Our study shows that obesity associated with sarcopenia exhibits significantly greater insulin resistance and dyslipidemia than sarcopenia or obesity per se. Therefore, sarcopenic obesity might be an independent risk factor for metabolic disease progression.
肌肉减少症、肥胖指数与代谢失调之间的关联仍存在争议。我们旨在评估和比较患有肌肉减少症和未患肌肉减少症的肥胖沙特成年男性的胰岛素抵抗和代谢状况。
这项横断面研究在利雅得的沙特国王大学体育科学学院进行。我们招募了312名沙特成年男性个体,最终288人被选入研究。所有受试者均通过生物电阻抗分析(BIA)和握力计分别进行身体成分分析和握力(HGS)评估。采集空腹血样检测血糖(FBG)、基础胰岛素(BI)和血脂谱。根据身体成分参数、四肢瘦体重(ALM)和体脂百分比(BF%)将受试者分为三组,即非肥胖组(NonOb)[正常ALM + <25% BF%]、无肌肉减少症的肥胖组(ObNonS)[正常ALM + >25% BF%]和有肌肉减少症的肥胖组(ObS)[低ALM + >25% BF%]。
与非肥胖者相比,肥胖受试者的BI、HOMA-IR和HOMA-β显著更高。此外,两个肥胖组之间的比较显示,ObS受试者的BI和HOMA-IR水平高于ObNonS个体,表明肌肉减少症会加剧胰岛素抵抗状况。从非肥胖到伴有肌肉减少症的肥胖,存在显著的更高抵抗和更低敏感性趋势。与无肌肉减少症的肥胖个体相比,有肌肉减少症的肥胖受试者的总胆固醇(TC)和甘油三酯(TG)显著更高,高密度脂蛋白胆固醇(HDL-C)显著更低。在胰岛素指标和血脂谱的截断点为7.46时,恶化效应更为显著,表明与肥胖相关的肌肉减少症会加剧血脂异常。
我们的研究表明,与肌肉减少症相关的肥胖比肌肉减少症或肥胖本身表现出显著更高的胰岛素抵抗和血脂异常。因此,肌肉减少性肥胖可能是代谢疾病进展的独立危险因素。