糖尿病合并骨质疏松患者血清C1q/肿瘤坏死因子相关蛋白3的表达及临床意义

Expression and clinical significance of serum C1q/tumor necrosis factor related protein 3 in diabetes patients complicated with osteoporosis

  • 摘要:
    目的 探讨血清C1q/肿瘤坏死因子相关蛋白3(CTRP3)在糖尿病合并骨质疏松患者中的表达水平及临床意义。
    方法 选取2020年1月-2021年12月收治的93例2型糖尿病合并骨质疏松患者为观察组,并以同期的80例单纯2型糖尿病患者为对照组。回顾性分析2组患者的人口学资料、糖脂代谢指标、骨代谢指标以及骨密度等临床资料,并采用酶联免疫吸附法检测2组血清CTRP3水平。采用多重线性回归分析血清CTRP3与糖脂代谢指标、骨代谢指标以及骨密度的相关性; 采用Logistic回归模型分析骨质疏松的影响因素; 采用受试者工作特征(ROC)曲线评估血清CTRP3对2型糖尿病患者骨质疏松的诊断价值。
    结果 观察组女性及吸烟史比率高于对照组,年龄大于对照组,糖尿病病程长于对照组,空腹血糖(FBG)、胰岛素抵抗指数(HOMA-IR)、空腹胰岛素(FINS)、糖化血红蛋白(HbA1c)、骨钙素N-端中分子片段(N-MID)、Ⅰ型胶原羧基端肽β-胶原特殊序列(β-CTX)、抗酒石酸盐酸性磷酸酶异构体5b(TRACP-5b)水平高于对照组,血清CTRP3水平、体质量指数(BMI)、骨密度、Ⅰ型前胶原氨基端前肽(PINP)、Ⅰ型前胶原羧基端前肽(PICP)、骨碱性磷酸酶(B-ALP)低于对照组,差异均有统计学意义(P < 0.05)。FBG、HOMA-IR、FINS、HbA1c、N-MID、β-CTX、TRACP-5b与CTRP3水平呈负相关(P < 0.05), PINP、PICP、B-ALP与CTRP3水平呈正相关(P < 0.05)。Logistic回归分析模型显示, FBG、HOMA-IR、FINS、HbA1c、CTRP3以及骨密度、骨代谢指标等均是2型糖尿病患者并发骨质疏松的独立影响因素(P < 0.05), 其中FBG、HOMA-IR、FINS、HbA1c、N-MID、β-CTX、TRACP-5b是危险因素(OR>1, P < 0.05), CTRP3、骨密度、PINP、PICP、B-ALP是保护因素(OR < 1, P < 0.05)。CTRP3诊断骨质疏松的曲线下面积(AUC)为0.815, 灵敏度和特异度分别为84.95%和63.75%; CTRP3联合骨密度诊断骨质疏松的AUC为0.882, 灵敏度和特异度分别为83.87%和78.75%。
    结论 糖尿病合并骨质疏松患者血清CTRP3表达下调,与糖代谢紊乱、骨代谢异常、骨密度降低密切相关,并可影响糖尿病患者骨质疏松的发生。

     

    Abstract:
    Objective To explore the expression level and clinical significance of serum C1q/tumor necrosis factor related protein 3 (CTRP3) in diabetes patients complicated with osteoporosis.
    Methods A total of 93 type 2 diabetes patients complicated with osteoporosis from January 2020 to December 2021 were selected as observation group, and 80 patients with simple type 2 diabetes in the same period were selected as control group. The clinical materials such as demographic data, glucose and lipid metabolism indicators, bone metabolism indicators and bone mineral density in both groups were retrospectively analyzed, and the serum CTRP3 level in both groups was detected by enzyme-linked immunosorbent assay. Multiple linear regression analysis was used to analyze the correlations of serum CTRP3 with glucose and lipid metabolism indicators, bone metabolism indicators and bone density; the Logistic regression model was used to analyze the influencing factors of osteoporosis; the receiver operating characteristic (ROC) curve was used to evaluate the value of serum CTRP3 in diagnosing type 2 diabetes patients complicated with osteoporosis.
    Results In the observation group, the ratios of female patients and patients with smoking history were significantly higher than those in the control group, the age was significantly older than that in the control group, the course of diabetes was significantly longer than that in the control group, the fasting blood glucose (FBG), insulin resistance index (HOMA-IR), fasting insulin (FINS), glycated hemoglobin (HbA1c), N-terminal middle molecular fragment of osteocalcin (N-MID), β isomer of C-terminal telopeptide of type Ⅰ collagen (β-CTX) and tartrate-resistant acid phosphatase 5b (TRACP-5b) levels were significantly higher than those in the control group, while serum CTRP3 level, body mass index (BMI), bone mineral density, propeptide of type Ⅰ procollagen (PINP), carboxyterminal propeptide of type Ⅰ procollagen (PICP) and bone alkaline phosphatase (B-ALP) were significantly lower than those in the control group (P < 0.05). FBG, HOMA-IR, FINS, HbA1c, N-MID, β-CTX and TRACP-5b were negatively correlated with CTRP3 level (P < 0.05), while PINP, PIC and B-ALP were positively correlated with CTRP3 level (P < 0.05). Logistic regression analysis model showed that FBG, HOMA-IR, FINS, HbA1c, CTRP and bone density as well as bone metabolism indicators were the independent influencing factors of type 2 diabetes patients complicated with osteoporosis (P < 0.05), of which FBG, HOMA-IR, FINS, HbA1c, N-MID, β-CTX and TRACP-5b were risk factors (OR>1, P < 0.05), and CTRP3, bone density, PINP, PICP and B-ALP were protective factors (OR < 1, P < 0.05). The area under the curve (AUC) of CTRP3 in diagnosing osteoporosis was 0.815, and the sensitivity and specificity were 84.95% and 63.75% respectively; the AUC of CTRP3 combined with BMD in diagnosing osteoporosis was 0.882, and the sensitivity and specificity were 83.87% and 78.75% respectively.
    Conclusion Serum CTRP3 is downregulated in diabetes patients with osteoporosis, and is closely related to glucose metabolism disorder, bone metabolism abnormality and bone density reduction, which can affect the occurrence of osteoporosis in diabetes patients.

     

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