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Effect of intensive insulin treatment on plasma levels of lipoprotein-associated phospholipase A 2 and secretory phospholipase A 2 in patients with newly diagnosed type 2 diabetes

View Article: PubMed Central - PubMed

ABSTRACT

Background: China has the highest absolute disease burden of diabetes worldwide. For diabetic patients, diabetes-related vascular complications are major causes of morbidity and mortality. The roles of lipoprotein-associated phospholipase A2 (Lp-PLA2) and secretory phospholipase A2 (sPLA2) as inflammatory markers have been recently evaluated in the pathogenesis of both diabetes and atherosclerosis. We aimed to determine the mechanism through which patients with newly diagnosed type 2 diabetes gain long-term vascular benefit from intensive insulin therapy by evaluating the change in Lp-PLA2 and sPLA2 levels after early intensive insulin treatment and its relevance with insulin resistance and pancreatic β-cell function.

Methods: In total, 90 patients with newly diagnosed type 2 diabetes mellitus were enrolled. All patients received continuous subcutaneous insulin infusion (CSII) for approximately 2 weeks. Intravenous glucose-tolerance test (IVGTT) and oral glucose-tolerance test (OGTT) were performed, and plasma concentrations of Lp-PLA2 and sPLA2 were measured before and after CSII.

Results: Levels of Lp-PLA2 and sPLA2 were significantly higher in diabetic patients with macroangiopathy than in those without (P < 0.05). After CSII, the sPLA2 level decreased significantly in all diabetic patients (P < 0.05), while the Lp-PLA2 level changed only in those with macroangiopathy (P < 0.05). The area under the curve of insulin in IVGTT and OGTT, the acute insulin response (AIR3–5), early phase of insulin secretion (ΔIns30/ΔG30), modified β-cell function index, and homeostatic model assessment for β-cell function (HOMA-β) increased after treatment even when adjusted for the influence of insulin resistance (IR; P < 0.001). The HOMA-IR was lower after treatment, and the three other indicators adopted to estimate insulin sensitivity (ISIced, IAI, and QUICKI) were higher after treatment (P < 0.05). Correlation analysis showed that the decrease in the Lp-PLA2 and sPLA2 levels was positively correlated with a reduction in HOMA-IR after CSII (P < 0.05). Additionally, multiple linear regression analysis showed that Lp-PLA2 and sPLA2 independently correlated with HOMA-IR (P < 0.05).

Conclusions: Lp-PLA2 and sPLA2 are closely related to insulin resistance and macroangiopathy in diabetic patients. Intensive insulin therapy might help improve IR and protect against diabetic macroangiopathy by influencing the Lp-PLA2 and sPLA2 levels.

Trial registration: ChiCTR-TRC-10001618 2010 September 16.

No MeSH data available.


Related in: MedlinePlus

Correlation between ΔLp-PLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.590, P < 0.05) (a); correlation between ΔsPLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.476, P < 0.05) (b). Values of P < 0.05 are statistically significant. ΔLp-PLA2, change in Lp-PLA2 levels; ΔsPLA2, change in sPLA2 levels; ΔHOMA-IR, change in homeostatic model assessment for insulin resistance
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Fig3: Correlation between ΔLp-PLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.590, P < 0.05) (a); correlation between ΔsPLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.476, P < 0.05) (b). Values of P < 0.05 are statistically significant. ΔLp-PLA2, change in Lp-PLA2 levels; ΔsPLA2, change in sPLA2 levels; ΔHOMA-IR, change in homeostatic model assessment for insulin resistance

Mentions: After CSII, the decrease in the Lp-PLA2 (ΔLp-PLA2) and sPLA2 (ΔsPLA2) levels were both positively correlated with the reduction in HOMA-IR (ΔHOMA-IR) (r = 0.590, P < 0.05 and r = 0.476, P < 0.05, respectively) (Fig. 3a, 3b). Further, multiple linear regression analysis showed that both Lp-PLA2 and sPLA2 levels were independent factors that were correlated with HOMA-IR (β = 0.372 and β = 0.560 respectively, P < 0.05).Fig. 3


Effect of intensive insulin treatment on plasma levels of lipoprotein-associated phospholipase A 2 and secretory phospholipase A 2 in patients with newly diagnosed type 2 diabetes
Correlation between ΔLp-PLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.590, P < 0.05) (a); correlation between ΔsPLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.476, P < 0.05) (b). Values of P < 0.05 are statistically significant. ΔLp-PLA2, change in Lp-PLA2 levels; ΔsPLA2, change in sPLA2 levels; ΔHOMA-IR, change in homeostatic model assessment for insulin resistance
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

License 1 - License 2
Show All Figures
getmorefigures.php?uid=PMC5120429&req=5

Fig3: Correlation between ΔLp-PLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.590, P < 0.05) (a); correlation between ΔsPLA2 and ΔHOMA-IR in diabetic patients after CSII (r = 0.476, P < 0.05) (b). Values of P < 0.05 are statistically significant. ΔLp-PLA2, change in Lp-PLA2 levels; ΔsPLA2, change in sPLA2 levels; ΔHOMA-IR, change in homeostatic model assessment for insulin resistance
Mentions: After CSII, the decrease in the Lp-PLA2 (ΔLp-PLA2) and sPLA2 (ΔsPLA2) levels were both positively correlated with the reduction in HOMA-IR (ΔHOMA-IR) (r = 0.590, P < 0.05 and r = 0.476, P < 0.05, respectively) (Fig. 3a, 3b). Further, multiple linear regression analysis showed that both Lp-PLA2 and sPLA2 levels were independent factors that were correlated with HOMA-IR (β = 0.372 and β = 0.560 respectively, P < 0.05).Fig. 3

View Article: PubMed Central - PubMed

ABSTRACT

Background: China has the highest absolute disease burden of diabetes worldwide. For diabetic patients, diabetes-related vascular complications are major causes of morbidity and mortality. The roles of lipoprotein-associated phospholipase A2 (Lp-PLA2) and secretory phospholipase A2 (sPLA2) as inflammatory markers have been recently evaluated in the pathogenesis of both diabetes and atherosclerosis. We aimed to determine the mechanism through which patients with newly diagnosed type 2 diabetes gain long-term vascular benefit from intensive insulin therapy by evaluating the change in Lp-PLA2 and sPLA2 levels after early intensive insulin treatment and its relevance with insulin resistance and pancreatic &beta;-cell function.

Methods: In total, 90 patients with newly diagnosed type 2 diabetes mellitus were enrolled. All patients received continuous subcutaneous insulin infusion (CSII) for approximately 2&nbsp;weeks. Intravenous glucose-tolerance test (IVGTT) and oral glucose-tolerance test (OGTT) were performed, and plasma concentrations of Lp-PLA2 and sPLA2 were measured before and after CSII.

Results: Levels of Lp-PLA2 and sPLA2 were significantly higher in diabetic patients with macroangiopathy than in those without (P&thinsp;&lt;&thinsp;0.05). After CSII, the sPLA2 level decreased significantly in all diabetic patients (P&thinsp;&lt;&thinsp;0.05), while the Lp-PLA2 level changed only in those with macroangiopathy (P&thinsp;&lt;&thinsp;0.05). The area under the curve of insulin in IVGTT and OGTT, the acute insulin response (AIR3&ndash;5), early phase of insulin secretion (&Delta;Ins30/&Delta;G30), modified &beta;-cell function index, and homeostatic model assessment for &beta;-cell function (HOMA-&beta;) increased after treatment even when adjusted for the influence of insulin resistance (IR; P&thinsp;&lt;&thinsp;0.001). The HOMA-IR was lower after treatment, and the three other indicators adopted to estimate insulin sensitivity (ISIced, IAI, and QUICKI) were higher after treatment (P&thinsp;&lt;&thinsp;0.05). Correlation analysis showed that the decrease in the Lp-PLA2 and sPLA2 levels was positively correlated with a reduction in HOMA-IR after CSII (P&thinsp;&lt;&thinsp;0.05). Additionally, multiple linear regression analysis showed that Lp-PLA2 and sPLA2 independently correlated with HOMA-IR (P&thinsp;&lt;&thinsp;0.05).

Conclusions: Lp-PLA2 and sPLA2 are closely related to insulin resistance and macroangiopathy in diabetic patients. Intensive insulin therapy might help improve IR and protect against diabetic macroangiopathy by influencing the Lp-PLA2 and sPLA2 levels.

Trial registration: ChiCTR-TRC-10001618 2010 September 16.

No MeSH data available.


Related in: MedlinePlus