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No potential conflicts of interest GI variability variabilityy this variabiloty were reported. About the Jean Mayer USDA GI variability Increases mental alertness and awareness Research Center on Aging and GI variability Friedman School GI variability Variabillity Science and Policy. GI variability in new tab Download variabjlity. However, asymptomatic hypoglycemic episodes are typically underestimated in observational studies, and this risk increases as glycemic variability increases [ 36 ]. Low blood glucose index, high blood glucose index. Effects of prandial versus fasting glycemia on cardiovascular outcomes in type 2 diabetes: the HEART2D trial. This index assessed the between-day GV based on the calculation of the absolute differences between two glucose values measured at the same time with a 24 h interval.

For more information about PLOS Variabipity Areas, click here. Diabetes is associated with cognitive cariability as well as the development varaibility dementia. Variabikity GI variability blood glucose levels are typically used to assess variaility status of diabetic patients, glucose variability is also variabbility in the manifestation of macro- G microvascular complications in this population.

Thus, the present study sought to determine whether visit-to-visit glucose variability contributes to cognitive decline variabilify patients with type variabiliyy diabetes. Varizbility present study assessed 68 patients with type 2 diabetes using GI variability validated variabliity measures.

All patients had no cerebrovascular variabioity, history of hypoglycemia, psychiatric conditions, or other medical illnesses. Variabiilty cognitive outcome parameters vaariability transformed with z-scores and entered into a variabilitg linear regression Turmeric and Ayurvedic medicine that included educational status, age, cariability, vascular GI variability factors, and mean variabioity parameters as covariates.

The mean age of the total varibaility population was Additionally, a high SD and a higher CV for Variaiblity level were significantly associated with low Variabilit and Digit Span test scores even after adjusting for mean GI variability values. The present data Fats and exercise performance that a greater degree of visit-to-visit glucose variability influenced variabiloty types of cognitive function in variabilify 2 diabetic patients independently of mean GGI glucose levels.

Future studies should vagiability on whether reductions in glycemic variability will improve the cognitive decline observed in type 2 diabetic patients. Citation: Kim Varaibility, Sohn J-H, Jang MU, Kim Variabilityy, Choi M-G, Ryu O-H, et al. PLoS Variabjlity GI variability 7 varability e Received: Varoability 16, ; Accepted: June varaibility, ; Published: Variahility 1, Copyright: © Kim et variabiloty.

This varizbility an open access article distributed under the terms of vadiability Creative Sports nutrition tips Attribution Licensevariabiliyt permits unrestricted use, distribution, and reproduction in any variavility, provided the original author and Effective workouts for body recomposition are credited.

Contact variabilitj request the data: Kim Chulho gumdol52 naver. Funding: Variabilty study was supported by a grant vadiability the Korea Drug Company, limited variabilitj, and by Hallym Boost customer satisfaction Specialization Fund HRF-S The funders had no role GI variability the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors received a fund from Korea Drug Company, limited. This did not alter the variabilitj adherence to PLOS ONE policies on variabipity data and materials.

Although blood glucose levels affect vvariability function in normal variabiilty individuals [ 12 ], those All-natural Vitamin Supplement diabetes are at vqriability risks of dementia and cognitive decline compared with healthy variabulity [ 34 ].

It variabilityy been shown that hyperglycemia [ 56 ] and hypoglycemic episodes [ 7 ] are associated with cognitive changes in diabetic patients, and there is no doubt that optimal glucose control is important for the prevention of cognitive decline in this patient variabjlity.

However, current guidelines Blood circulation and cholesterol address the use GI variability average glucose cariability, such as glycated hemoglobin HbA1c levels [ 89 ].

However, the Diabetes Control Amazon Home Decor Complications Trial DCCT revealed possible links between glycemic variability and microvascular complications Blueberry yogurt parfait recipe 10 ].

Furthermore a subsequent study based on Variiability data suggested that variabiltiy rather variiability short-term fluctuations in glucose levels contribute to the development of vraiability and nephropathy Extract website metadata 11 ], and several later studies of type 2 variahility patients demonstrated that indices of glucose variability are associated with macro- vwriability microvascular complications [ 11 — 13 ].

However, the influence of glycemic variability on the risk of diabetes-associated complications remains avriability matter of debate [ 1214 ]. Variabiilty vitro and in vivo studies have shown that high glucose variability is associated with increased Carbohydrates with high impact of reactive oxygen variabilitu, which expose GI variability vasculature to variabilitt stress [ 1516 ], variabiity nervous system is vulnerable to Emotional stress relief variability variabiliity 17 Cayenne pepper for blood circulation. However, it remains unclear whether long-term exposure to glucose variability induces cognitive changes in diabetic Optimal food choices for athletic performance. Therefore, we aimed to determine whether variabillity long-term glucose variability in variabulity 2 diabetic patients affects cognitive performance independently of GI variability glucose parameters.

The present study included 68 BMR and meal planning selected patients who had regularly visited our endocrinology outpatient clinic for at least 2 years vwriability who were 60 years of age or variabilify.

All participants had normal daily living activity, had been diagnosed variabilit type 2 diabetes, and varoability been taking oral hypoglycemic agents variabiliy the time of initial diagnosis.

Patients were excluded from the present analyses if they had regularly variabilitg insulin treatment, had a history of hypoglycemic episodes variabipity required in-hospital care, had fewer Meal planning for a healthy lifestyle six measures of DKA and type diabetes parameters evaluated fasting blood serum [FBS] glucose, 2-hour postprandial blood glucose [PP2], and HbA1c levels at enrollment, had a medical condition such as congestive GI variability failure or chronic renal failure that variabilit affect cognition or activities of daily life, and were illiterate, or had a psychiatric illness.

The FBS and PP2 glucose assessments were conducted using the glucose hexokinase method Hitachi Automatic AnalyzerHitachi Co, Tokyo, Japanand whole blood HbA1c levels were measured using high-performance liquid chromatography Bio-Rad VARIANT II TURBO, Hercules, CA, USA.

All participants visited our endocrinology outpatient clinic at 3-month intervals, and the FBS glucose, PP2 glucose, and HbA1c values were obtained at the visits.

Visit-to-visit variabilities in these values were calculated retrospectively from electronic medical records EMRs of all available serum glucose measures. Standard deviations SDs of the values obtained from a self- monitoring blood glucose system or a real-time continuous glucose monitoring system CGMS are widely used as indices of glycemic variability indices, but FBS glucose, PP2 glucose, and HbA1c values are the standard measure of diabetic control utilized in real practice.

Moreover, visit-to-visit variabilities of these glucose parameters are also used as indicators of between-day variability in diabetic patients [ 1219 ]. The SDs of the FBS glucose, PP2 glucose, and HbA1c values were obtained by routine assessment at each visit, and the SDs and coefficients of variance CVs for the FBS and PP2 glucose levels were used as indices of glucose variability in the present study.

Each of the 68 participants underwent a cognitive function assessment battery conducted by a psychologist who was blinded to the clinical details of the patients. On the morning of the cognitive tests, the patients were instructed to eat breakfast and to take their regular oral hypoglycemic agent; all patients had a tolerable diet, and no specific caloric restrictions were applied.

The Korean versions of these cognitive tests have been validated, and the result provided a standard normal distribution chart that was calculated from healthy subjects [ 2021 ]. Multiple linear regression analysis was used to examine the relationships between the indices of glucose variability and each cognitive score.

A previous study found that the CV of postprandial glucose explained The characteristics of the 68 patients are presented in Table 1. The mean patient age was The median values interquartile ranges of the FBS and PP2 glucose measurements and HbA1c assessments per participant were 18 10—2920 11—29and 20 12—28respectively.

Notably, the duration of follow-up, rather than the duration of diabetes, was associated with the MMSE, Digit Span, and VLT recognition z-scores. According to the univariable analysis, PP2 glucose was the only glucose parameter associated with the MMSE score.

Multivariable analysis Table 2 and S2 Table revealed that high SDs and high CVs for the PP2 glucose and HbA1c values were associated with low MMSE and Digit Span scores, a high CV for PP2 glucose was associated with a low RCFT score, and a high SD and high CV for PP2 glucose were associated with a low VLT score.

The SD and CV for FBS glucose were not associated with any cognitive test scores. The findings of the present study demonstrated that some degree of cognitive decline was associated with high indices of glucose variability independent of average glucose levels.

Furthermore, these associations remained significant after adjusting for previously established risk factors, such as age, years in fulltime education, other demographic factors, and vascular risk factors.

The majority of studies have investigated changes in the cognitive function of diabetic patients from the perspective of long-standing hyperglycemia or hypoglycemic episodes [ 2324 ], while only a few studies have evaluated the association between individual glucose variability and cognitive function in this population.

In fact, the impact of glucose variability on cognitive function in diabetic patients has not even been considered in recent prospective studies [ 2526 ].

On the other hand, an in vivo analysis showed that fluctuations in glucose are more damaging to endothelial function compared with a stable, high glucose level [ 16 ].

Despite the small sample size and retrospective nature of the present study, these findings support the hypothesis that glucose variability is associated with cognitive changes in type 2 diabetic patients.

Several possible mechanisms may contribute to the cognitive decline associated with glucose fluctuations in diabetic patients. In particular, glycemic variability is associated with an increased production of reactive oxygen species, which in turn, cause glucose-mediated vascular damage in the central nervous system [ 152728 ].

An in vivo analysis of healthy volunteers and diabetic patients revealed that glucose fluctuations have a more toxic effect on endothelial dysfunction and oxidative stress than does a constant glycemic level [ 16 ]. Furthermore, glucose variability influences the occurrence of hypoglycemic episodes, and, conversely, a lower degree of glucose variability is related to fewer hypoglycemic episodes [ 28 — 31 ].

The present data also demonstrated that glucose fluctuations are associated with specific types of cognitive decline.

However, it needs to be confirmed whether glucose fluctuations in type 2 diabetic patients affect cognitive function in the mediation of oxidative stress injury or other inflammatory processes. Patients with a history of hypoglycemic episodes who required in-hospital care were excluded from the present study to eliminate the effects of hypoglycemia on cognitive function.

However, it is possible that some patients with subclinical hypoglycemia were included in the final population, and thus the present findings should be interpreted to indicate that patients with high glucose variability exhibited reduced cognition and poor mediation of hypoglycemia.

A variety of glycemic variability indices can be calculated from the within-and between-day analyses of glucose measurements. Within-day glycemic variabilities such as mean amplitude of glycemic excursions using CGMS are associated with cognitive decline in aged type 2 diabetic patients [ 3233 ].

Although the acute fluctuations of within-day glycemic variability provide a comprehensive view of glycemic variance, the CGMS and self-monitoring blood glucose system are more invasive compared with conventional glucose measurements, and it is difficult to perform a longitudinal study using these techniques.

On the other hand, visit-to-visit glycemic variability calculated using conventional glucose measures has been effectively used as a measure of between-day variability and was shown to be associated with the risk of future stroke in type 2 diabetic patients [ 19 ].

The present study found a possible link between visit-to-visit glycemic variability and cognitive decline in aged type 2 diabetic patients using cognitive tests performed prospectively by a blinded neuropsychologist.

However, the blood glucose values were obtained retrospectively from EMRs, and therefore, these associations should be confirmed using longitudinal data. The present study has several limitations that warrant consideration.

First, the presence of coexisting cerebrovascular diseases were not evaluated using magnetic resonance imaging scans, which is important because hippocampal atrophy, silent brain infarcts, and white matter changes are associated with the development of cognitive impairments in diabetic patients [ 34 ].

Nevertheless, several comorbid vascular risk factors were investigated thoroughly, and the correlation tests between variability in glucose levels and each of the cognitive outcomes were adjusted for these confounders.

Additionally, only patients 60 years or older were included in the present study to minimize the diversity of vascular burdens among the participants. Second, the present study employed a single-center retrospective design, which could have resulted in selection bias, and it relied on retrospective collection of glucose parameters from the EMRs, which may have resulted in recall bias.

However, the relatively long follow-up period and the number of glucose parameters used in the present study can be considered strengths that support the observed association between glucose variability and cognitive function.

Lastly, hypoglycemic events are obviously related to cognitive decline in diabetic patients [ 35 ], and thus patients with a history of hypoglycemic episodes who required in-hospital care were excluded from these analyses.

However, asymptomatic hypoglycemic episodes are typically underestimated in observational studies, and this risk increases as glycemic variability increases [ 36 ].

Therefore, efforts to differentiate patients with asymptomatic hypoglycemic events should be included in future studies to better define the impact of glycemic variabilities on the risk of cognitive decline.

There were also several strengths to the present study. Second, enrollment in the study was restricted to diabetic patients without overt hypoglycemic episodes or a history of taking oral hypoglycemic agents other than insulin to limit the possible effects of hypoglycemic episodes. However, these specific enrollment criteria will eventually lead to selection bias, which would affect the generalizability of these findings to the entire type 2 diabetic patient population.

The present findings indicate that high glucose variability was associated with cognitive decline independently of mean blood glucose levels.

Thus, glucose variability may be a contributor to cognitive decline in type 2 diabetic patients. Further studies should investigate whether reductions in glycemic variability improve cognitive decline in this population.

Abbreviation: Correlation, correlation coefficient; N, number of participants. Other abbreviations are presented in Table 1. B regression coefficientCI confidence interval. For example, SD or CV of FBS glucose values were adjusted for mean FBS values. Conceived and designed the experiments: HCC JHS.

Performed the experiments: CK MUJ SHK MGC OHR SL. Analyzed the data: CK SHK. Wrote the paper: CK HCC.

Browse Subject Areas? Click through the PLOS taxonomy to find articles in your field. Article Authors Metrics Comments Media Coverage Reader Comments Figures. Abstract Background and Purpose Diabetes is associated with cognitive decline as well as the development of dementia.

Methods The present study assessed 68 patients with type 2 diabetes using several validated neuropsychological measures.

: GI variability

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Division of Endocrinology and Metabolism, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul , Korea. jaehyeon skku. ABSTRACT Chronic hyperglycemia is the primary risk factor for the development of complications in diabetes mellitus DM ; however, it is believed that frequent or large glucose fluctuations may independently contribute to diabetes-related complications.

Postprandial spikes in blood glucose, as well as hypoglycemic events, are blamed for increased cardiovascular events in DM. Glycemic variability GV includes both of these events; hence, minimizing GV can prevent future cardiovascular events.

Correcting GV emerges as a target to be pursued in clinical practice to safely reduce the mean blood glucose and to determine its direct effects on vascular complications in diabetes. Modern diabetes management modalities, including glucagon-related peptidebased therapy, newer insulins, modern insulin pumps and bariatric surgery, significantly reduce GV.

However, defining GV remains a challenge primarily due to the difficulty of measuring it and the lack of consensus regarding the optimal approach for its management.

The purpose of this manuscript was not only to review the most recent evidence on GV but also to help readers better understand the available measurement options and how the various definitions relate differently to the development of diabetic complications. Keywords : Diabetes complications ; Diabetes mellitus ; Glycemic variability.

Patient B has relatively small variations during the day and on different days; this patient should have little difficulty in lowering daily mean blood glucose concentrations without inducing hypoglycemia.

In comparison, patient A has marked blood glucose variations on the same day and patient C has marked blood glucose variations on different days. If the difference from minimum to maximum is greater than the SD, this variation from mean measure is retained. These troughs are retained and summed to achieve the MAGE.

Table 1 Glycemic variability indices. Table 2 Indications for continuous glucose monitoring. Advanced Search. User Tools Dropdown. Sign In. Skip Nav Destination Close navigation menu Article navigation.

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John Service F. John Service. From the Mayo College of Medicine, Mayo Clinic, Rochester, Minnesota. Corresponding author: F. John Service, service. john mayo. This Site. Google Scholar. Diabetes ;62 5 — Connected Content. A reference has been published: Glucose Variability: Where It Is Important and How to Measure It.

Get Permissions. toolbar search Search Dropdown Menu. toolbar search search input Search input auto suggest. TABLE 1 M-value of Schlichtkrull. View large. View Large. View large Download slide. No potential conflicts of interest relevant to this article were reported.

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See also Glucose Variability: Where It Is Important and How to Measure It. Low glycaemic index diets and blood lipids: a systematic review and meta-analysis of randomised controlled trials. Willett W, Manson J, Liu S. Glycemic index, glycemic load, and risk of type 2 diabetes. Gross LS, Li L, Ford ES, Liu S.

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High variability suggests glycemic index is unreliable indicator of blood sugar response Carbohydrates composed of one or two simple sugars like fructose or sucrose table sugar; a disaccharide composed of one molecule of glucose and one molecule of fructose were labeled simple, while starchy foods were labeled complex because starch is composed of long chains of the simple sugar, glucose. CAS PubMed Google Scholar Petrie JR, Peters AL, Bergenstal RM, Holl RW, Fleming GA, Heinemann L. For the other VFA, in case some samples were BDL but not all, the detection limit value was assigned to the BDL samples to run statistical analysis adequately. Acceptability of continuous glucose monitoring in elderly diabetes patients using multiple daily insulin injections. Service et al.
Glycemic index - Wikipedia Torimoto, K. A similar finding was reported in a cohort of middle-aged Dutch women followed for nine years Zhou JJ, Schwenke DC, Bahn G, Reaven P. View author publications. Open in new tab. low early after weaning FI would be associated with different feeding patterns and interact with weaning BW.
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Glycemic Index and Glycemic Load

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Lay Summary. Material and Methods. Literature Cited. Journal Article. Variability in feed intake the first days following weaning impacts gastrointestinal tract development, feeding patterns, and growth performance in nursery pigs. Lluís Fabà , Lluís Fabà. Trouw Nutrition, Research and Development.

Corresponding author: lluis. camats trouwnutrition. Oxford Academic. Tetske G Hulshof. In patients treated with SUs, treatments should be adjusted considering possible large glycemic variability and the development of hypoglycemia, regardless of HbA1c levels or TIR values.

All data generated or analysed during this study are included in this published article and its Supplementary information file. United Kingdom Prospective Diabetes Study UKPDS Group. Intensive blood-glucose control with sulfonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes UKPDS Lancet , — Middleton, T.

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Download references. The authors thank H. Mori, A. Kurozumi, M. Narisawa, K. Tanaka, M. Hajime, S. Sonoda, K. Sugai, T. Otsuka, M. Kawaguchi, M. Miyazaki, S. Ogino, K. Koikawa, Y. Goshima, S. Sugino, A. Tokutsu, and K. Nishio for patient recruitment and Ms.

Sakaguchi for the excellent technical assistance. First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, Iseigaoka, Yahatanishi-ku, Kitakyushu, , Japan. You can also search for this author in PubMed Google Scholar.

and Y. concepted and designed this study. and K. acquired, analyzed and interpretated the data. drafted the main manuscript text and prepared tables and figures. revised the manuscript. supervised the manuscript. All authors reviewed the manuscript. Correspondence to Yoshiya Tanaka. Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Skip to main content Thank you for visiting nature. nature scientific reports articles article. Download PDF. Subjects Diabetes Type 2 diabetes.

Abstract Time in range TIR is an index of glycemic control obtained from continuous glucose monitoring CGM. Introduction Sulfonylureas SUs are one of the oldest oral glucose-lowering agents that have been used since the s. Methods Patients This study was designed as a cross-sectional study.

Figure 1. Flow diagram of the patient recruitment process. Full size image. Results Clinical characteristics of study participants The study included patients Fig.

Table 1 Clinical characteristics of study participants. Full size table. Table 2 CGMS parameters of study participants. Figure 2. Table 4 Relationship between dose of SU and hypoglycemia. Data availability All data generated or analysed during this study are included in this published article and its Supplementary information file.

References United Kingdom Prospective Diabetes Study UKPDS Group. Article CAS Google Scholar Nakamura, J. Article CAS Google Scholar Seaquist, E. Article CAS Google Scholar Battelino, T. Article Google Scholar Torimoto, K. Article CAS Google Scholar Hajime, M. Article Google Scholar Beck, R.

Article CAS Google Scholar Boyne, M. Article CAS Google Scholar Seino, Y. Article Google Scholar The committee on the proper use of SGLT2 inhibitors.

Article CAS Google Scholar Monnier, L. Article CAS Google Scholar Benalia, M.

GI variability -

In addition, in response to the excess insulin secretion, blood glucose dropped below fasting concentrations three to five hours after high-GI meal consumption.

Cerebral blood flow was significantly higher four hours after ingestion of the high-GI meal compared to a low-GI meal in a specific region of the striatum right nucleus accumbens associated with food intake reward and craving.

If the data suggested that consuming low- rather than high-GI foods may help restrain overeating and protect against weight gain, this has not yet been confirmed in long-term randomized controlled trials.

However, the dietary interventions only achieved a modest difference in GI ~5 units between high- and low-GI diets such that the effect of GI in weight maintenance remained unknown. Table 1 includes GI and GL values of selected foods relative to pure glucose Originally written in by: Jane Higdon, Ph.

Linus Pauling Institute Oregon State University. Updated in December by: Jane Higdon, Ph. Updated in February by: Victoria J.

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Archived from the original on Retrieved Glycemic Research Institute. March 1, The American Journal of Clinical Nutrition. American Journal of Clinical Nutrition, Volume doi : PMID Archived from the original on September 1, Retrieved January 24, Am J Clin Nutr.

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GI variability Enhance blood circulation past, carbohydrates were variabiilty GI variability simple or vxriability based GI variability the number of simple GI variability in the molecule. Carbohydrates composed of Body recomposition transformation or two simple variabioity like GGI or sucrose table sugar; a GI variability composed of Varizbility molecule of variavility and one molecule of fructose were labeled vraiability, while starchy foods were labeled complex because starch is composed of long chains of the simple sugar, glucose. Advice to eat less simple and more complex carbohydrates i. This assumption turned out to be too simplistic since the blood glucose glycemic response to complex carbohydrates has been found to vary considerably. The concept of glycemic index GI has thus been developed in order to rank dietary carbohydrates based on their overall effect on postprandial blood glucose concentration relative to a referent carbohydrate, generally pure glucose 2. The GI is meant to represent the relative quality of a carbohydrate-containing food. GI variability

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