Bakillah Ahmed, Al Subaiee Maram, Obeid Khamis Khamees, Soliman Ayman Farouk, Al Otaibi Abeer, Mubarak Sindiyan Al Shaikh, Al Mihmadi Yara Abdullah, Bashir Shahinaz Faisal, Al Arab Mohammad, Al Hussaini Arwa, Al Qarni Ali Ahmed
King Abdullah International Medical Research Center (KAIMRC), Al Ahsa 36428, Saudi Arabia.
Biomedical Research Core, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Al Ahsa 36428, Saudi Arabia.
Nutrients. 2025 Sep 6;17(17):2883. doi: 10.3390/nu17172883.
: Cardiovascular disease (CVD) is the leading cause of mortality in obese patients with type 2 diabetes mellitus (T2DM). Conventional biomarkers often fail to detect early endothelial dysfunction and oxidative stress. Haptoglobin (Hp), an acute-phase protein with antioxidant and hemoglobin-binding properties, may indicate vascular injury. While plasma Hp (pl-Hp) reflects systemic inflammation, urinary Hp (u-Hp) could signal renal and microvascular damage. We hypothesize that elevated u-Hp and altered pl-Hp levels are associated with increased oxidized LDL and may serve as sensitive indicators of early vascular injury, thereby identifying obese patients with T2DM at higher cardiovascular risk. This study aims to investigate the associations between u-Hp, pl-Hp, and oxidized LDL (ox-LDL) in obese patients with T2DM, and to evaluate the potential role of Hp as an early biomarker of cardiovascular risk in this high-risk population. : The study included 57 patients with T2DM (mean age 61 ± 10 years, HbA1c 8.66 ± 1.60%, and BMI 35.15 ± 6.65 kg/m). Notably, 95% of the patients had hypertension, 82% had dyslipidemia, and 59% had an estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m. Pl-Hp and u-Hp concentrations, as well as ox-LDL levels, were assessed using an enzyme-linked immunosorbent assay (ELISA). Correlations and multivariate regression analyses were employed to investigate the associations between Hp, ox-LDL, and clinical cardiovascular risk factors. Pl-Hp was positively correlated with ox-LDL (r = 0.358, < 0.006) and negatively correlated with C-reactive protein (CRP) (r = -0.364, < 0.013), while u-Hp correlated positively with HbA1C and apoB levels (r = 0.298, < 0.030 and r = 0.310, < 0.021, respectively). Multivariate analysis indicated that pl-Hp, but not u-Hp, was independently associated with ox-LDL (β = 0.536, < 0.027) after adjusting for potential confounding factors, including age, gender, BMI, HbA1c, liver enzymes, hs-CRP and creatinine. The Stepwise analysis identified IL-6 as the most significant predictor of cardiovascular disease risk, suggesting its pivotal role in subclinical vascular inflammation among obese individuals with T2DM. Furthermore, the significant positive association between pl-Hp and ox-LDL was stronger in patients with declining renal function as expressed by the estimated glomerular filtration rate (eGFR) (eGFR < 30 mL/min/1.73 m: β = 2.173, < 0.031 and eGFR 30-59 mL/min/1.73 m: β = 1.318, < 0.002). This association also appeared in early and low-normal ranges of serum albumin: creatinine ratio (s-ACR) (s-ACR < 0.2714 mg/mmol: β = 2.304, < 0.005 and s-ACR 0.2714-0.3649 mg/mmol: β = 1.000, < 0.041), suggesting that pl-Hp and ox-LDL rise before overt kidney damage. Elevated IL-6 (≥32.93 pg/mL) further strengthened this link (β = 1.037, < 0.005), highlighting the role of inflammation in amplifying oxidative stress and acute-phase responses. : Taken together, these findings emphasize the interconnected contributions of renal impairment, inflammation, and oxidative stress to vascular injury. While these results need to be confirmed in larger prospective longitudinal studies, monitoring pl-Hp levels in conjunction with inflammatory and kidney function markers could be a sensitive and non-invasive way to identify early CVD risk in high-risk groups, such as obese patients with T2DM.
心血管疾病(CVD)是肥胖的2型糖尿病(T2DM)患者死亡的主要原因。传统生物标志物常常无法检测到早期内皮功能障碍和氧化应激。触珠蛋白(Hp)是一种具有抗氧化和血红蛋白结合特性的急性期蛋白,可能提示血管损伤。血浆Hp(pl-Hp)反映全身炎症,而尿Hp(u-Hp)可能提示肾脏和微血管损伤。我们假设尿Hp升高和血浆Hp水平改变与氧化型低密度脂蛋白(ox-LDL)增加有关,可能作为早期血管损伤的敏感指标,从而识别出心血管风险较高的肥胖T2DM患者。本研究旨在探讨肥胖T2DM患者尿Hp、血浆Hp与氧化型低密度脂蛋白(ox-LDL)之间的关联,并评估Hp作为这一高危人群心血管风险早期生物标志物的潜在作用。
该研究纳入了57例T2DM患者(平均年龄61±10岁,糖化血红蛋白8.66±1.60%,体重指数35.15±6.65kg/m)。值得注意的是,95%的患者患有高血压,82%的患者患有血脂异常,59%的患者估计肾小球滤过率(eGFR)<60mL/min/1.73m²。采用酶联免疫吸附测定(ELISA)评估血浆Hp和尿Hp浓度以及ox-LDL水平。采用相关性和多变量回归分析来研究Hp、ox-LDL与临床心血管危险因素之间的关联。血浆Hp与ox-LDL呈正相关(r=0.358,P<0.006),与C反应蛋白(CRP)呈负相关(r=-0.364,P<0.013),而尿Hp与糖化血红蛋白A1C(HbA1C)和载脂蛋白B水平呈正相关(分别为r=0.298,P<0.030和r=0.310,P<0.021)。多变量分析表明,在调整了年龄、性别、体重指数、糖化血红蛋白、肝酶、高敏CRP和肌酐等潜在混杂因素后,血浆Hp而非尿Hp与ox-LDL独立相关(β=0.536,P<0.027)。逐步分析确定白细胞介素-6(IL-6)是心血管疾病风险的最显著预测因子,表明其在肥胖T2DM患者亚临床血管炎症中的关键作用。此外,根据估计肾小球滤过率(eGFR),肾功能下降患者中血浆Hp与ox-LDL之间的显著正相关更强(eGFR<30mL/min/1.73m²:β=2.173,P<0.031;eGFR 30-59mL/min/1.73m²:β=1.318,P<0.002)。这种关联在血清白蛋白:肌酐比值(s-ACR)的早期和低正常范围内也出现(s-ACR<0.2714mg/mmol:β=2.304,P<0.005;s-ACR 0.2714-0.3649mg/mmol:β=1.000,P<0.041),提示血浆Hp和ox-LDL在明显肾脏损伤之前升高。IL-6升高(≥32.93pg/mL)进一步加强了这种联系(β=1.037,P<0.005),突出了炎症在放大氧化应激和急性期反应中的作用。
综上所述,这些发现强调了肾功能损害、炎症和氧化应激对血管损伤的相互作用。虽然这些结果需要在更大规模的前瞻性纵向研究中得到证实,但结合炎症和肾功能标志物监测血浆Hp水平可能是一种敏感且无创的方法,用于识别高危人群如肥胖T2DM患者的早期心血管疾病风险。