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疑似反应性低血糖患者的代谢参数

Metabolic Parameters in Patients with Suspected Reactive Hypoglycemia.

作者信息

Hall Marianna, Walicka Magdalena, Panczyk Mariusz, Traczyk Iwona

机构信息

Department of Human Nutrition, Faculty of Health Sciences, Medical University of Warsaw, 01-445 Warsaw, Poland.

Department of Internal Diseases, Endocrinology and Diabetology, Central Clinical Hospital of the Ministry of Internal Affairs and Administration in Warsaw, 02-507 Warsaw, Poland.

出版信息

J Pers Med. 2021 Apr 7;11(4):276. doi: 10.3390/jpm11040276.

DOI:10.3390/jpm11040276
PMID:33916952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8067537/
Abstract

BACKGROUND

It remains unclear whether reactive hypoglycemia (RH) is a disorder caused by improper insulin secretion, result of eating habits that are not nutritionally balanced or whether it is a psychosomatic disorder. The aim of this study was to investigate metabolic parameters in patients admitted to the hospital with suspected RH.

METHODS

The study group (SG) included non-diabetic individuals with symptoms consistent with RH. The control group (CG) included individuals without hypoglycemic symptoms and any documented medical history of metabolic disorders. In both groups the following investigations were performed: fasting glucose and insulin levels, Homeostatic Model Assessment for Insulin Resistance (HOMA-IR), 75 g five-hour Oral Glucose Tolerance Test (OGTT) with an assessment of glucose and insulin and lipid profile evaluation. Additionally, Mixed Meal Tolerance Test (MMTT) was performed in SG. Results from OGTT and MMTT were analyzed in line with the non-standardized RH diagnostic criteria.

RESULTS

Forty subjects have been enrolled into SG. Twelve (30%) of those patients had hypoglycemic symptoms and glucose level ≤55 mg/dL during five-hour OGTT and have been diagnosed with RH. Ten (25%) subjects manifested hypoglycemic like symptoms without significant glucose decline. Patients with diagnosed RH had statistically significantly lower mean glucose at first (92.1 ± 37.9 mg/dL vs. 126.4 ± 32.5 mg/dL; LSD test: < 0.001) and second (65.6 ± 19.3 mg/dL vs. 92.6 ± 19.3 mg/dL; LSD test: < 0.001) hour of OGTT and insulin value (22.7 ± 10.9 lU/mL vs. 43.4 ± 35.0 lU/mL; LSD test: < 0.001) at second hour of OGTT compared to the patients who did not meet the criteria of RH. Seventeen (43%) subjects from SG reported symptoms suggesting hypoglycemia during MMTT but none of them had glucose value lower than ≤55 mg/dL (68.7 ± 4.7 mg/dL). From the entire lipid profile, only mean total cholesterol value was significantly higher ( = 0.024) in SG in comparison with CG but did not exceed standard reference range.

CONCLUSIONS

No metabolic disturbances have been observed in patients with diagnosed reactive hypoglycemia. Hyperinsulinemia has not been associated with glycemic declines in patients with this condition. Occurrence of pseudohypoglicemic symptoms and lower glucose value was more common after ingestion of glucose itself rather than after ingestion of a balanced meal. This could suggest an important role that nutritionally balanced diet may play in maintaining correct glucose and insulin levels in the postprandial period.

摘要

背景

反应性低血糖(RH)究竟是由胰岛素分泌不当引起的疾病,还是营养不均衡饮食习惯的结果,抑或是一种心身疾病,目前仍不清楚。本研究的目的是调查疑似患有RH而入院的患者的代谢参数。

方法

研究组(SG)包括有与RH相符症状的非糖尿病个体。对照组(CG)包括没有低血糖症状且无任何代谢紊乱病史记录的个体。两组均进行了以下检查:空腹血糖和胰岛素水平、胰岛素抵抗稳态模型评估(HOMA-IR)、75克五小时口服葡萄糖耐量试验(OGTT),并评估葡萄糖、胰岛素及血脂情况。此外,对研究组进行了混合餐耐量试验(MMTT)。根据非标准化的RH诊断标准分析OGTT和MMTT的结果。

结果

40名受试者被纳入研究组。其中12名(30%)患者在五小时OGTT期间出现低血糖症状且血糖水平≤55毫克/分升,被诊断为RH。10名(25%)受试者表现出类似低血糖的症状,但血糖无明显下降。与未达到RH标准的患者相比,确诊为RH的患者在OGTT的第一小时(92.1±37.9毫克/分升对126.4±32.5毫克/分升;LSD检验:<0.001)和第二小时(65.6±19.3毫克/分升对92.6±19.3毫克/分升;LSD检验:<0.001)的平均血糖以及OGTT第二小时的胰岛素值(22.7±10.9国际单位/毫升对43.4±35.0国际单位/毫升;LSD检验:<0.001)在统计学上显著更低。研究组中有17名(43%)受试者在MMTT期间报告有提示低血糖的症状,但他们中没有一人血糖值低于≤55毫克/分升(68.7±4.7毫克/分升)。在整个血脂谱中,与对照组相比,研究组仅平均总胆固醇值显著更高(P = 0.024),但未超过标准参考范围。

结论

确诊为反应性低血糖的患者未观察到代谢紊乱。高胰岛素血症与该疾病患者的血糖下降无关。假低血糖症状的出现和较低的血糖值在摄入葡萄糖后比摄入均衡餐后更常见。这可能表明营养均衡的饮食在维持餐后正确的血糖和胰岛素水平方面可能发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/9e0019559e83/jpm-11-00276-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/ba42287a8c43/jpm-11-00276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/dcaffb358768/jpm-11-00276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/a3e1cefd86ce/jpm-11-00276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/9e0019559e83/jpm-11-00276-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/ba42287a8c43/jpm-11-00276-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/dcaffb358768/jpm-11-00276-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/a3e1cefd86ce/jpm-11-00276-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7739/8067537/9e0019559e83/jpm-11-00276-g004.jpg

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