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心脏利钠肽、肥胖和胰岛素抵抗:来自两项基于社区的研究的证据。

Cardiac natriuretic peptides, obesity, and insulin resistance: evidence from two community-based studies.

机构信息

Cardiology Division, Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

J Clin Endocrinol Metab. 2011 Oct;96(10):3242-9. doi: 10.1210/jc.2011-1182. Epub 2011 Aug 17.

Abstract

BACKGROUND

The natriuretic peptides play an important role in salt homeostasis and blood pressure regulation. It has been suggested that obesity promotes a relative natriuretic peptide deficiency, but this has been a variable finding in prior studies and the cause is unknown.

AIM

The aim of this study was to examine the association between obesity and natriuretic peptide levels and evaluate the role of hyperinsulinemia and testosterone as mediators of this interaction.

METHODS

We studied 7770 individuals from the Framingham Heart Study (n = 3833, 54% women) and the Malmö Diet and Cancer study (n = 3918, 60% women). We examined the relation of plasma N-terminal pro-B-type natriuretic peptide levels (N-BNP) with obesity, insulin resistance, and various metabolic subtypes.

RESULTS

Obesity was associated with 6-20% lower levels of N-BNP (P < 0.001 in Framingham, P = 0.001 in Malmö), whereas insulin resistance was associated with 10-30% lower levels of N-BNP (P < 0.001 in both cohorts). Individuals with obesity who were insulin sensitive had only modest reductions in N-BNP compared with nonobese, insulin-sensitive individuals. On the other hand, individuals who were nonobese but insulin resistant had 26% lower N-BNP in Framingham (P < 0.001) and 10% lower N-BNP in Malmö (P < 0.001), compared with nonobese and insulin-sensitive individuals. Adjustment for serum-free testosterone did not alter these associations.

CONCLUSIONS

In both nonobese and obese individuals, insulin resistance is associated with lower natriuretic peptide levels. The relative natriuretic peptide deficiency seen in obesity could be partly attributable to insulin resistance, and could be one mechanism by which insulin resistance promotes hypertension.

摘要

背景

利钠肽在盐稳态和血压调节中发挥着重要作用。有研究表明,肥胖会导致相对利钠肽缺乏,但这在之前的研究中结果不一,其原因尚不清楚。

目的

本研究旨在探讨肥胖与利钠肽水平之间的关系,并评估高胰岛素血症和睾酮在这种相互作用中的作用。

方法

我们研究了弗雷明汉心脏研究(n = 3833,54%为女性)和马尔默饮食与癌症研究(n = 3918,60%为女性)中的 7770 名个体。我们检测了血浆 N 末端脑利钠肽前体(N-BNP)水平与肥胖、胰岛素抵抗以及各种代谢亚型的关系。

结果

肥胖与 N-BNP 水平降低 6%-20%相关(弗雷明汉的 P < 0.001,马尔默的 P = 0.001),而胰岛素抵抗与 N-BNP 水平降低 10%-30%相关(两个队列的 P < 0.001)。与非肥胖、胰岛素敏感的个体相比,胰岛素敏感的肥胖个体的 N-BNP 仅有适度降低。另一方面,与非肥胖、胰岛素敏感的个体相比,非肥胖但胰岛素抵抗的个体在弗雷明汉的 N-BNP 降低 26%(P < 0.001),在马尔默的 N-BNP 降低 10%(P < 0.001)。调整血清游离睾酮后,这些关联并未改变。

结论

在非肥胖和肥胖个体中,胰岛素抵抗与利钠肽水平降低有关。肥胖中观察到的相对利钠肽缺乏可能部分归因于胰岛素抵抗,这可能是胰岛素抵抗促进高血压的机制之一。

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