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      Glycaemic thresholds for counterregulatory hormone and symptom responses to hypoglycaemia in people with and without type 1 diabetes: a systematic review

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          Abstract

          Aim/hypothesis

          The physiological counterregulatory response to hypoglycaemia is reported to be organised hierarchically, with hormone responses usually preceding symptomatic awareness and autonomic responses preceding neuroglycopenic responses. To compare thresholds for activation of these responses more accurately between people with or without type 1 diabetes, we performed a systematic review on stepped hyperinsulinaemic–hypoglycaemic glucose clamps.

          Methods

          A literature search in PubMed and EMBASE was conducted. We included articles published between 1980 and 2018 involving hyperinsulinaemic stepped hypoglycaemic glucose clamps among people with or without type 1 diabetes. Key exclusion criteria were as follows: data were previously published; other patient population; a clamp not the primary intervention; and an inadequate clamp description. Glycaemic thresholds for counterregulatory hormone and/or symptom responses to hypoglycaemia were estimated and compared using generalised logrank test for interval-censored data, where the intervals were either extracted directly or calculated from the data provided by the study. A glycaemic threshold was defined as the glucose level at which the response exceeded the 95% CI of the mean baseline measurement or euglycaemic control clamp. Because of the use of interval-censored data, we described thresholds using median and IQR.

          Results

          A total of 63 articles were included, whereof 37 papers included participants with type 1 diabetes ( n=559; 67.4% male sex, aged 32.7±10.2 years, BMI 23.8±1.4 kg/m 2) and 51 papers included participants without diabetes ( n=733; 72.4% male sex, aged 31.1±9.2 years, BMI 23.6±1.1 kg/m 2). Compared with non-diabetic control individuals, in people with type 1 diabetes, the median (IQR) glycaemic thresholds for adrenaline (3.8 [3.2–4.2] vs 3.4 [2.8–3.9 mmol/l]), noradrenaline (3.2 [3.2–3.7] vs 3.0 [2.8–3.1] mmol/l), cortisol (3.5 [3.2–4.2]) vs 2.8 [2.8–3.4] mmol/l) and growth hormone (3.8 [3.3–3.8] vs. 3.2 [3.0–3.3] mmol/l) all occurred at lower glucose levels in people with diabetes than in those without diabetes (all p≤0.01). Similarly, although both autonomic (median [IQR] 3.4 [3.4–3.4] vs 3.0 [2.8–3.4] mmol/l) and neuroglycopenic (median [IQR] 3.4 [2.8–N/A] vs 3.0 [3.0–3.1] mmol/l) symptom responses were elicited at lower glucose levels in people with type 1 diabetes, the thresholds for autonomic and neuroglycopenic symptoms did not differ for each individual subgroup.

          Conclusions/interpretation

          People with type 1 diabetes have glycaemic thresholds for counterregulatory hormone and symptom responses at lower glucose levels than people without diabetes. Autonomic and neuroglycopenic symptoms responses are generated at about similar levels of hypoglycaemia. There was a considerable variation in the methodology of the articles and the high insulin doses in most of the clamps may affect the counterregulatory responses.

          Funding

          This article has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement no. 777460.

          Registration

          This systematic review is registered in PROSPERO (CRD42019120083).

          Graphical abstract

          Supplementary Information

          The online version contains peer-reviewed but unedited supplementary material available at 10.1007/s00125-022-05749-8.

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          Most cited references77

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          • Article: not found

          Hypoglycemia in diabetes.

          Iatrogenic hypoglycemia causes recurrent morbidity in most people with type 1 diabetes and many with type 2 diabetes, and it is sometimes fatal. The barrier of hypoglycemia generally precludes maintenance of euglycemia over a lifetime of diabetes and thus precludes full realization of euglycemia's long-term benefits. While the clinical presentation is often characteristic, particularly for the experienced individual with diabetes, the neurogenic and neuroglycopenic symptoms of hypoglycemia are nonspecific and relatively insensitive; therefore, many episodes are not recognized. Hypoglycemia can result from exogenous or endogenous insulin excess alone. However, iatrogenic hypoglycemia is typically the result of the interplay of absolute or relative insulin excess and compromised glucose counterregulation in type 1 and advanced type 2 diabetes. Decrements in insulin, increments in glucagon, and, absent the latter, increments in epinephrine stand high in the hierarchy of redundant glucose counterregulatory factors that normally prevent or rapidly correct hypoglycemia. In insulin-deficient diabetes (exogenous) insulin levels do not decrease as glucose levels fall, and the combination of deficient glucagon and epinephrine responses causes defective glucose counterregulation. Reduced sympathoadrenal responses cause hypoglycemia unawareness. The concept of hypoglycemia-associated autonomic failure in diabetes posits that recent antecedent hypoglycemia causes both defective glucose counterregulation and hypoglycemia unawareness. By shifting glycemic thresholds for the sympathoadrenal (including epinephrine) and the resulting neurogenic responses to lower plasma glucose concentrations, antecedent hypoglycemia leads to a vicious cycle of recurrent hypoglycemia and further impairment of glucose counterregulation. Thus, short-term avoidance of hypoglycemia reverses hypoglycemia unawareness in most affected patients. The clinical approach to minimizing hypoglycemia while improving glycemic control includes 1) addressing the issue, 2) applying the principles of aggressive glycemic therapy, including flexible and individualized drug regimens, and 3) considering the risk factors for iatrogenic hypoglycemia. The latter include factors that result in absolute or relative insulin excess: drug dose, timing, and type; patterns of food ingestion and exercise; interactions with alcohol and other drugs; and altered sensitivity to or clearance of insulin. They also include factors that are clinical surrogates of compromised glucose counterregulation: endogenous insulin deficiency; history of severe hypoglycemia, hypoglycemia unawareness, or both; and aggressive glycemic therapy per se, as evidenced by lower HbA(1c) levels, lower glycemic goals, or both. In a patient with hypoglycemia unawareness (which implies recurrent hypoglycemia) a 2- to 3-week period of scrupulous avoidance of hypoglycemia is advisable. Pending the prevention and cure of diabetes or the development of methods that provide glucose-regulated insulin replacement or secretion, we need to learn to replace insulin in a much more physiological fashion, to prevent, correct, or compensate for compromised glucose counterregulation, or both if we are to achieve near-euglycemia safely in most people with diabetes.
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            • Record: found
            • Abstract: not found
            • Article: not found

            Glucose Concentrations of Less Than 3.0 mmol/L (54 mg/dL) Should Be Reported in Clinical Trials: A Joint Position Statement of the American Diabetes Association and the European Association for the Study of Diabetes.

            (2016)
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              Hypoglycemia in type 2 diabetes: pathophysiology, frequency, and effects of different treatment modalities.

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                Author and article information

                Contributors
                clementine.verhulst@radboudumc.nl
                therese.emilie.wilbek.fabricius@regionh.dk
                Journal
                Diabetologia
                Diabetologia
                Diabetologia
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0012-186X
                1432-0428
                22 July 2022
                22 July 2022
                2022
                : 65
                : 10
                : 1601-1612
                Affiliations
                [1 ]GRID grid.10417.33, ISNI 0000 0004 0444 9382, Department of Internal Medicine, , Radboud University Medical Centre, ; Nijmegen, the Netherlands
                [2 ]GRID grid.414092.a, ISNI 0000 0004 0626 2116, Department of Endocrinology and Nephrology, , Nordsjællands Hospital, ; Hillerød, Denmark
                [3 ]GRID grid.10417.33, ISNI 0000 0004 0444 9382, Section Biostatistics, Department for Health Evidence, Radboud Institute for Health Sciences, , Radboud University Medical Centre, ; Nijmegen, the Netherlands
                [4 ]GRID grid.5254.6, ISNI 0000 0001 0674 042X, Department of Clinical Medicine, Faculty of Health and Medical Sciences, , University of Copenhagen, ; Copenhagen, Denmark
                [5 ]GRID grid.8241.f, ISNI 0000 0004 0397 2876, School of Medicine, , University of Dundee, ; Dundee, Scotland
                [6 ]GRID grid.11835.3e, ISNI 0000 0004 1936 9262, Department of Oncology and Metabolism, , University of Sheffield, ; Sheffield, UK
                [7 ]GRID grid.5335.0, ISNI 0000000121885934, Wellcome Trust/MRC Institute of Metabolic Science, , University of Cambridge, ; Cambridge, UK
                [8 ]GRID grid.13097.3c, ISNI 0000 0001 2322 6764, Department of Diabetes, School of Life Course Sciences, Faculty of Life Sciences & Medicine, , King’s College London, ; London, UK
                [9 ]GRID grid.412966.e, ISNI 0000 0004 0480 1382, Department of Internal Medicine, Division of Endocrinology, , Maastricht University Medical Centre, ; Maastricht, the Netherlands
                [10 ]GRID grid.5012.6, ISNI 0000 0001 0481 6099, CARIM School for Cardiovascular Diseases, , Maastricht University, ; Maastricht, the Netherlands
                Author information
                https://orcid.org/0000-0002-9905-7669
                https://orcid.org/0000-0002-6344-5408
                https://orcid.org/0000-0003-4103-7451
                https://orcid.org/0000-0001-5431-824X
                https://orcid.org/0000-0003-0322-1653
                https://orcid.org/0000-0002-3957-1981
                https://orcid.org/0000-0002-2425-9565
                https://orcid.org/0000-0001-8122-8987
                https://orcid.org/0000-0003-2686-5531
                https://orcid.org/0000-0003-0588-4880
                https://orcid.org/0000-0002-1255-7741
                Article
                5749
                10.1007/s00125-022-05749-8
                9477942
                35867127
                914fd017-fbbd-4e71-bbf7-307db40170ca
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 November 2021
                : 6 May 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100010661, Horizon 2020 Framework Programme;
                Award ID: 777460
                Categories
                Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2022

                Endocrinology & Diabetes
                counterregulatory hormones,diabetes,glycaemic thresholds,human,hyperinsulinaemic–hypoglycaemic stepped clamp,hypoglycaemia,symptomatic responses; systematic review

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