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1 uppressed the fetal femoral vasoconstrictor, glycaemic and lactate acidaemic responses during hypoxia
2                                              Glycaemic and lipid factors may play a vasoconstrictive
3 uded changes in uric acid concentrations and glycaemic and lipid variables.
4                              Here we analyse glycaemic and metabolic control, cardiovascular risk, me
5 l follow-up identified enduring and emerging glycaemic and metformin legacy treatment effects.
6              Differences between clusters in glycaemic and renal progression were investigated and co
7 There were no significant differences across glycaemic categories in median LDL cholesterol at baseli
8 he incidence of the primary endpoint in each glycaemic category, but a greater absolute reduction in
9                                        Rapid glycaemic change in patients with uncontrolled diabetes
10 xposure, or were switched to the alternative glycaemic condition, or to an intermediate glucose conce
11 d endothelial cells between hyper- and normo-glycaemic conditions on bioenergetic and functional para
12 on was the same when adjusted for centre and glycaemic control (0.55 [0.30-1.03], p = 0.06).
13  type 2 diabetes mellitus who had inadequate glycaemic control (glycosylated haemoglobin [HbA(1c)] 7.
14 es in blood pressure, total cholesterol, and glycaemic control (haemoglobin A1c) after 2 years.
15 .0-12.6], p=0.0004), mainly through improved glycaemic control (HbA1c <7.0% [53 mmol/mol] in 45 [75%]
16  They were eligible when they had suboptimum glycaemic control (HbA1c 7.1-11.0% [54-97 mmol/mol]) des
17 8 years) with type 2 diabetes and inadequate glycaemic control (HbA1c 8-12% [64-108 mmol/mol]) despit
18                         Associations between glycaemic control (HbA1c), episodes of diabetic ketoacid
19 with diagnosed diabetes, (2) proportion with glycaemic control (measured HbA(1c) <7.0%), (3) proporti
20 or if overweight, metformin) or conventional glycaemic control (primarily diet).
21 a 3 month run-in to optimise risk factor and glycaemic control (single-blind placebo in the final mon
22 ndomly allocated to receive either intensive glycaemic control (sulfonylurea or insulin, or if overwe
23                    Clinical risk factors and glycaemic control alone cannot predict the development o
24  diabetes overall and by different levels of glycaemic control and albuminuria.
25 n to reduce the risk of diabetes and improve glycaemic control and blood lipids in patients with diab
26                                         Poor glycaemic control and consequent increased HbA(1c) level
27 or factor that contributes to long-term poor glycaemic control and diabetic ketoacidosis in this age
28                                         Poor glycaemic control and impaired renal function substantia
29                                 The inferior glycaemic control and increased risk of hypoglycaemia wi
30 dies have characterised the relation between glycaemic control and infectious disease, which we discu
31 c modulator of hGPR40, demonstrates improved glycaemic control and low hypoglycaemic risk in diabetic
32 nced microvascular perfusion, contributes to glycaemic control and maintenance of vascular health, st
33                               Disparities in glycaemic control and other areas of care may lead to hi
34 iabetes, there are improvements in long-term glycaemic control and psychological distress but not in
35 e and liraglutide have been shown to improve glycaemic control and reduce bodyweight in patients with
36 in delivery is a promising option to improve glycaemic control and reduce the risk of hypoglycaemia.
37 us insulin therapy has been shown to improve glycaemic control and reduce the risk of long-term compl
38 peptide-1 (GLP-1) receptor agonists, improve glycaemic control and reduce weight in patients with typ
39 T-2 inhibitor therapy significantly improves glycaemic control and reduces bodyweight in patients wit
40 a glucagon-like peptide-1 analogue, improves glycaemic control and reduces bodyweight in patients wit
41 ith type 1 diabetes increased with worsening glycaemic control and renal complications.
42 fects on cardiovascular risk factors such as glycaemic control and reverse cholesterol transport.
43 owever, many patients do not achieve optimum glycaemic control and therefore new therapies are necess
44 efficacy and tolerability, provided superior glycaemic control and weight loss compared with sitaglip
45 tter treatment approaches for achieving good glycaemic control are badly needed.
46 ment of depression as well as improvement in glycaemic control as a marker for subsequent diabetes ou
47 es mellitus and are associated with improved glycaemic control as well as with reductions in body mas
48 s with relapse, however, maintained adequate glycaemic control at 10 years (mean HbA(1c) 6.7% [SD 0.2
49 ion (measured by C-peptide) and provision of glycaemic control at reduced doses of insulin if they ta
50 tide was the most effective GLP-1RA drug for glycaemic control by reducing haemoglobin A(1c) and fast
51                                       Strict glycaemic control can decrease development and progressi
52 y closed-loop insulin delivery would improve glycaemic control compared with conventional subcutaneou
53 tor agonist treatment, resulting in improved glycaemic control compared with its components given alo
54 om health-care professionals offers superior glycaemic control compared with support from health-care
55 of vascular risk factors and optimisation of glycaemic control could have therapeutic benefit.
56 ients with type 2 diabetes mellitus and poor glycaemic control despite insulin therapy, with or witho
57   Patients with type 2 diabetes who had poor glycaemic control despite multiple daily injections with
58                Mean HbA1c was used to assess glycaemic control during follow-up.
59 reatment of type 2 diabetes have been led by glycaemic control for decades.
60                                    Intensive glycaemic control had no significant effect on events of
61                                 At 6 months, glycaemic control had worsened in the control group (mea
62         Intensive insulin therapy with tight glycaemic control has been advocated for improving outco
63 ct to insulin therapy in IDDM, might improve glycaemic control in adolescents; we investigated the ef
64 a do not support use of metformin to improve glycaemic control in adults with long-standing type 1 di
65  that severe periodontitis adversely affects glycaemic control in diabetes and glycaemia in non-diabe
66  diagnostic assays for the long-term mark of glycaemic control in diabetes.
67 chological problems are associated with poor glycaemic control in diabetes.
68          Intensive treatment to achieve good glycaemic control in diabetic patients is limited by a h
69 s suggest setting individualised targets for glycaemic control in elderly patients with type 2 diabet
70 lts of randomised controlled trials of tight glycaemic control in hospital inpatients might vary with
71                                         Good glycaemic control in insulin-dependent diabetes mellitus
72 und, has been shown to significantly improve glycaemic control in large-scale clinical trials, and sh
73 de could be considered for the management of glycaemic control in middle-aged and older people with t
74                                       Poorer glycaemic control in participants with known diabetes wa
75  is an effective treatment option to improve glycaemic control in patients receiving nutritional supp
76 gest that sacubitril/valsartan might enhance glycaemic control in patients with diabetes and HFrEF.
77 sing adjunct treatment to insulin to improve glycaemic control in patients with inadequately controll
78 Whether these actions contribute to improved glycaemic control in patients with insulin resistance wa
79 view aims to appraise the evidence for tight glycaemic control in patients with neurological injury.
80 d the effect of dapagliflozin-saxagliptin on glycaemic control in patients with type 2 diabetes and m
81                                      Optimum glycaemic control in patients with type 2 diabetes is im
82 TERPRETATION: TAK-875 significantly improved glycaemic control in patients with type 2 diabetes with
83 -like peptide-1 (GLP-1) receptor agonist for glycaemic control in patients with type 2 diabetes.
84 educe hepatic fat content (HFC) and increase glycaemic control in pre-diabetic patients with non-alco
85 europathy caused by an abrupt improvement in glycaemic control in the setting of chronic hyperglycaem
86                    The evidence for improved glycaemic control in the treatment of depression by use
87                                    Effective glycaemic control in type 1 diabetes mellitus usually re
88 s to assess their effectiveness in improving glycaemic control in type 2 diabetes.
89 rent clinical use in improving post-prandial glycaemic control in type 2 diabetics.
90                                Comprehensive glycaemic control information should account for more th
91 nt intensification leading to sustained good glycaemic control is essential to delay diabetic complic
92 n this age group, and evidence suggests that glycaemic control is often neglected.
93             However, continued monitoring of glycaemic control is warranted because of potential rela
94                                        Tight glycaemic control may result in hypoglycaemia, which in
95               The main outcome was long-term glycaemic control measured by percentage of glycated hae
96       INTERPRETATION: Our findings show that glycaemic control measured by time in the glucose range
97                                Durability of glycaemic control might reduce disease burden and improv
98                Evidence suggests that better glycaemic control might reduce infection risk, but furth
99 se prandial insulin intensification provides glycaemic control non-inferior to a full basal-bolus reg
100                         The deterioration in glycaemic control observed in patients aged 10-20 years
101 tic subtype defines treatment, with improved glycaemic control on sulfonylurea treatment for most pat
102                           No therapy altered glycaemic control or body weight.
103                                        Tight glycaemic control reduces microvascular complications in
104 or the treatment of type 2 diabetes, optimum glycaemic control remains challenging for many patients
105                                    Intensive glycaemic control resulted in a 17% reduction in events
106                   Although diabetes and poor glycaemic control significantly increase the risk of tub
107    Overall, intensive compared with standard glycaemic control significantly reduces coronary events
108                       Target-based intensive glycaemic control strategies (RR 1.00, 95% CI 0.88-1.13;
109 ess of a continuous, day-and-night automated glycaemic control system using insulin and glucagon has
110  were randomly assigned to receive intensive glycaemic control targeting HbA(1c) to less than 6.0% (4
111  There is more uncertainty about appropriate glycaemic control targets in this age group, and evidenc
112 ovided significantly greater improvements in glycaemic control than did exenatide twice a day, and wa
113 ed in a significantly greater improvement in glycaemic control than did glargine and represents a new
114 essation is associated with deterioration in glycaemic control that lasts for 3 years and is unrelate
115 lbumin are markers of short-term (2-4 weeks) glycaemic control that might add complementary prognosti
116 l prescription of blood pressure, lipid, and glycaemic control treatments for adults with type 2 diab
117                                        Worse glycaemic control was associated with increased risk of
118 uration of diabetes in late midlife and poor glycaemic control were associated with accelerated cogni
119 rmin (>/=1500 mg per day) and had inadequate glycaemic control were randomly assigned to receive one
120 l tests, vibration perception-threshold, and glycaemic control were unchanged.
121 rofile of longer than 42 h, provided similar glycaemic control when injected three times a week (IDeg
122 ance of monitoring fetal growth and maternal glycaemic control when treating GDM.
123 ype 1 diabetes because it provides effective glycaemic control while lowering the risk of nocturnal h
124 preparations has the potential for improving glycaemic control with a high degree of patient acceptan
125 th type 2 diabetes who do not achieve target glycaemic control with conventional insulin treatment, a
126 ts with type 2 diabetes who had insufficient glycaemic control with diet and exercise alone.
127 e 2 diabetes in patients who have inadequate glycaemic control with metformin alone.
128 type 2 diabetes who did not achieve adequate glycaemic control with metformin alone.
129 ged 18 years and older, who had insufficient glycaemic control with metformin either alone or in comb
130 n for patients who do not achieve sufficient glycaemic control with metformin therapy.
131 apagliflozin in patients who have inadequate glycaemic control with metformin.
132 ients with type 2 diabetes mellitus improved glycaemic control without hypoglycaemia risk.
133 ncentrations to less than 8 mmol/L (moderate glycaemic control), while avoiding mild hypoglycaemia (<
134  prior glycaemic exposure despite subsequent glycaemic control, a phenomenon called metabolic memory.
135 es, including fear of hypoglycaemia, loss of glycaemic control, and inadequate knowledge around exerc
136 ther owners experience facilitated tightened glycaemic control, and wider psychosocial benefits.
137 uction (plasma lipid levels, blood pressure, glycaemic control, body weight and non-smoking status).
138 otential value of alert dogs, for increasing glycaemic control, client independence and consequent qu
139 t, adverse effects of periodontal disease on glycaemic control, diabetes complications, and developme
140       Our findings suggest that disparity in glycaemic control, diabetes-related monitoring, and pres
141 n treatment is thought to contribute to poor glycaemic control, diabetic ketoacidosis, and brittle di
142  characterized by excess adiposity, impaired glycaemic control, dyslipidaemia and moderate hypertensi
143 rary data as to whether disparities exist in glycaemic control, monitoring, and prescribing in people
144 address high unmet medical need via improved glycaemic control, several clinical trials have been don
145 enhanced prevention measures preoperatively (glycaemic control, skin decontamination, decolonisation,
146 rticipants, their age, duration of diabetes, glycaemic control, type of psychological therapy, its mo
147               Maternal outcome measures were glycaemic control, weight gain, and treatment failure.
148                                         Good glycaemic control, which reduces long-term diabetes comp
149 once weekly exenatide led to improvements in glycaemic control, with greater reductions noted with li
150 once weekly exenatide led to improvements in glycaemic control, with greater reductions noted with li
151 ion within 8 weeks of a large improvement in glycaemic control-specified as a decrease in glycosylate
152  and we consider alternatives for monitoring glycaemic control.
153 ride-exposed groups, independent of maternal glycaemic control.
154 lyses show small to moderate improvements in glycaemic control.
155 -cell mass and insulin content, and improves glycaemic control.
156  they are unlikely to be related to improved glycaemic control.
157 es is dependent on both disease duration and glycaemic control.
158         CD diagnosis does not impact on T1DM glycaemic control.
159 most effective treatment for weight loss and glycaemic control.
160 ere is little evidence that it may influence glycaemic control.
161 etary means for type 2 diabetics to exercise glycaemic control.
162 HbA(1c) of <7% and 37% had very poor (>/=9%) glycaemic control.
163 o glucose monitoring is required for tighter glycaemic control.
164 ntervention soon after diagnosis can improve glycaemic control.
165 nd brain volume of intensive versus standard glycaemic control.
166 tment, with comparatively little effect from glycaemic control.
167 pies improves person-centred outcomes beyond glycaemic control.
168 ving metabolic health, weight management and glycaemic control.
169 y be used as a bioactive food ingredient for glycaemic control.
170 s cardiovascular disease and a wide range of glycaemic control.
171 uctions in cardiovascular risk achieved with glycaemic control.
172 ting persistent vascular dysfunction despite glycaemic control.
173  increased with renal complications and poor glycaemic control.
174 t-transplant diabetes; establish the role of glycaemic control; and assess the role of new diabetic t
175 ellitus (GDM) is directly linked to maternal glycaemic control; however, this relationship may be alt
176 se of the high levels of glycaemia and rapid glycaemic deterioration noted in this population.
177                    Prediabetes is a state of glycaemic dysregulation below the diagnostic threshold o
178  in advance of the development of obesity or glycaemic dysregulation.
179 xposure to HFD well in advance of obesity or glycaemic dysregulation.
180       We aimed to compare blood pressure and glycaemic effects of the SGLT2 inhibitor dapagliflozin w
181  not yet available to establish for how long glycaemic efficacy could be sustained during long-term t
182                                              Glycaemic efficacy of Technosphere inhaled insulin is lo
183 etes are limited and have demonstrated lower glycaemic efficacy than those for adult-onset type 2 dia
184 ability can represent the presence of excess glycaemic excursions and, consequently, the risk of hype
185  In patients with type 1 or type 2 diabetes, glycaemic exposure assessed as HbA1c correlates strongly
186 elated genes and phenotypes induced by prior glycaemic exposure despite subsequent glycaemic control,
187                               5-year risk of glycaemic failure was lower in model-concordant versus m
188 tment decisions for achieving individualised glycaemic goals with minimal risk in this important popu
189  insulin, most patients do not meet clinical glycaemic goals, and diabetes remains an important medic
190 d profile, body composition, and fitness and glycaemic goals.
191  immune signalling, microbial translocation, glycaemic health and blood transcriptome in the wild-bor
192 o indicate potential for improvements in non-glycaemic health outcomes from CGM use.
193 lopment of dietary strategies to improve the glycaemic impact of starch-rich meals which could be tes
194 arbohydrate digestion to make foods of lower glycaemic impact.
195                                       Lowest glycaemic index (54.58) and the highest sensory scores (
196 ture, in vitro starch digestibility, in vivo glycaemic index (GI) and sensorial properties of biscuit
197 rial (RCT), of a lifestyle intervention (low glycaemic index (GI) diet plus physical activity) in pre
198  Clinical studies suggest a role for dietary glycaemic index (GI) in bodyweight regulation and diabet
199   This study addressed determinations of the glycaemic index (GI), antioxidant capacity (AC), and phe
200 enhanced nutritional characteristics and low glycaemic index (GI).
201 s employed to assess the effect on simulated glycaemic index (GI).
202                      Carbohydrates with high glycaemic index are proposed to promote the development
203            Dietary carbohydrates with a high glycaemic index cause a high postprandial glucose and in
204  as an alternative in the elaboration of low glycaemic index foods.
205                  MBB, WBB, OSB and MSB had a glycaemic index of 75+/-4, 71+/-5, 68+/-5 and 65+/-4, re
206              This study examined whether the glycaemic index of dietary carbohydrates is a determinan
207 PS) in reducing the starch digestibility and glycaemic index of noodles was investigated.
208  serum HDL-cholesterol concentration and the glycaemic index of the diet for both men (regression coe
209                                    Thus, the glycaemic index of the diet is a stronger predictor than
210 s-sectional study of middle-aged adults, the glycaemic index of the diet was the only dietary variabl
211                                The estimated glycaemic index was higher in breads with higher hydrati
212 activity and reduced phytic acid content and glycaemic index, although a slight decrease in in vitro
213 ics, including the type of carbohydrate, the glycaemic index, and fat intake.
214  dietary patterns such as Mediterranean, low glycaemic index, moderately low carbohydrate, and vegeta
215 eads demonstrated better texture and reduced glycaemic index.
216 l ingredient in various foods to possess low-glycaemic index.
217 urdough fermentation with a presumable lower glycaemic index.
218 cated by impaired hypoglycaemia awareness or glycaemic lability, or who already receive immunosuppres
219 gnitude of the femoral vasoconstriction, the glycaemic, lactacidaemic and acidaemic responses and the
220 ated with the level of glycated haemoglobin, glycaemic level, and time of disease onset.
221  21 and 56) to determine the level of GI and glycaemic load (GL).
222 ntervention group, including reduced dietary glycaemic load, gestational weight gain, and maternal su
223                 Compared with standard care, glycaemic lowering by various drugs or strategies might
224  efficacy of continuous, multiday, automated glycaemic management has not been tested in outpatient s
225 he long-term benefits and risks of automated glycaemic management with a bihormonal bionic pancreas.
226  generation of biofunctional ingredients for glycaemic management.
227 hat can be prevented or delayed by intensive glycaemic management.
228     Haemoglobin A1c (HbA1c) is a significant glycaemic marker for diabetes mellitus.
229 exenatide and dapagliflozin improved various glycaemic measures and cardiovascular risk factors in pa
230  status, while also assessing its effects on glycaemic measures including risk of new-onset diabetes.
231 e converted systematically between different glycaemic metrics.
232 promote physiological adaptations, including glycaemic mobilization and corticosterone release.
233 icians dealing with patients with suboptimal glycaemic outcomes should be aware of these potential is
234                           We aimed to assess glycaemic outcomes when switching from multiple daily in
235 -0.846), and after additional adjustment for glycaemic parameters (model-2, OR: 0.670, 95%CI: 0.511-0
236  for T2DM must show meaningful reductions in glycaemic parameters as well as cardiovascular safety.
237 r of the MALT1 gene, involved in insulin and glycaemic pathways, and related to taurocholate levels i
238 nnel abnormality can result in a fluctuating glycaemic phenotype.
239 uous clinical features (age at diagnosis for glycaemic progression and baseline renal function for re
240               Clusters showed differences in glycaemic progression, but a model using age at diagnosi
241 auses of monogenic diabetes helps understand glycaemic regulation in humans.
242                          Novel approaches to glycaemic regulation include use of inhibitors of the so
243 ng sequentially numbered sealed envelopes to glycaemic regulation with a bihormonal bionic pancreas o
244 icipant weight, was able to achieve superior glycaemic regulation without the need for carbohydrate c
245 icipant weight, was able to achieve superior glycaemic regulation without the need for carbohydrate c
246 ways, including altered absorption kinetics, glycaemic response and the gut microbiota composition an
247             A similar trend was observed for glycaemic response in vivo.
248 ns could be an innovative route to alter the glycaemic response of carbohydrate-rich foods.
249 monstrate that patients vary widely in their glycaemic response to critical illness and response to i
250                                              Glycaemic response to metformin is heritable, thus glyca
251 mic response to metformin is heritable, thus glycaemic response to metformin is, in part, intrinsic t
252    We aimed to establish the heritability of glycaemic response to metformin using the genome-wide co
253                          The heritability of glycaemic response to metformin varied by response pheno
254 whom 2085 had enough clinical data to define glycaemic response to metformin.
255 stimate heritability for four definitions of glycaemic response to metformin: absolute reduction in H
256                  We aimed to see whether the glycaemic response to the sulphonylurea gliclazide and t
257 sed in the treatment of type 2 diabetes, but glycaemic response to this drug is highly variable.
258                         Clusters differed in glycaemic response, with a particular benefit for thiazo
259 antagonistic or synergic effect on predicted glycaemic response.
260  and steamed bread was healthier in terms of glycaemic response.
261 d to an antagonistic effect on the predicted glycaemic response.
262 ration conditions, is a major determinant of glycaemic response.
263 y diminished the femoral vasoconstrictor and glycaemic responses to hypoxaemia, and attenuated the in
264                                    Combining glycaemic results with clinical information improves pro
265 ct of alirocumab on cardiovascular events by glycaemic status at baseline (diabetes, prediabetes, or
266 51.1 years [SD 12.7]) with available data on glycaemic status from at least one follow-up visit were
267 sed to quantify the effect of previous (DPP) glycaemic status on risk of later (DPPOS) diabetes and n
268 fects on cardiovascular outcomes by baseline glycaemic status, while also assessing its effects on gl
269 patients of acromegaly irrespective of their glycaemic status.
270  insoluble fibre, essential amino acids, low glycaemic sugars, resistant to thermal food processing a
271                               Individualised glycaemic target levels are achievable with vildagliptin
272 of life that are independent of a particular glycaemic target.
273 es and anti-hyperglycaemic therapies emerge, glycaemic targets will continue to evolve.
274 atment option for patients unable to achieve glycaemic targets with conventional insulin treatment.
275 ight management is as important as attaining glycaemic targets.
276             The AUC for the three underlying glycaemic tests was 65.0% (95% CI 63.0-66.9) for HbA(1c)
277 ) [HbA(1c)] of <6.0%) or standard (7.0-7.9%) glycaemic therapy.
278 tion of remission should include unambiguous glycaemic thresholds and emphasise duration.
279 and categorised by glucose-lowering therapy, glycaemic thresholds, and duration.
280  and 232 (87%) definitions specified numeric glycaemic thresholds.
281  cases, 76 344 non-cases; five studies), and glycaemic traits (concentrations of fasting glucose, 2-h
282 ce for an association between depression and glycaemic traits (eg, glucose, insulin, insulin sensitiv
283 otyped studies of CAD, MI, diabetes, lipids, glycaemic traits and adiposity to obtain unconfounded es
284 which have been previously linked to fasting glycaemic traits and insulin resistance in genome wide a
285 ney function, adiposity, metabolic syndrome, glycaemic traits or blood lipid concentrations).
286                                              Glycaemic traits such as fasting and post-challenge gluc
287 endelian randomisation-derived estimates for glycaemic traits were not significant (p>0.25).
288 etes, adiposity, blood pressure, lipids, and glycaemic traits), using two-sample Mendelian randomizat
289 D concentration with type 2 diabetes and the glycaemic traits, and compared them with that from a met
290  recent advances in the genetic aetiology of glycaemic traits, and the resulting biological insights.
291 to the discovery of over 97 loci influencing glycaemic traits.
292 blood-based metabolic traits, in addition to glycaemic values, could optimise estimation of diabetes
293 00 h) glycaemia (incremental AUC [iAUC]) and glycaemic variability (%coefficient of variation [%CV])
294 t evidence examining the association between glycaemic variability and diabetes-related complications
295 flexibility, and a somewhat higher degree of glycaemic variability and hypoglycaemia when compared to
296 dent risk factor for diabetes complications, glycaemic variability can represent the presence of exce
297                                              Glycaemic variability is an integral component of glucos
298                                              Glycaemic variability is currently defined by a large an
299 ay and between-day variability) or long-term glycaemic variability, which is usually based on serial
300 h-risk state for diabetes that is defined by glycaemic variables that are higher than normal, but low

 
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