The Promise of Adjunct Medications in Improving Type 1 Diabetes Outcomes: Glucagon-like Peptide Receptor Agonists DOI Creative Commons
Sujatha Seetharaman, Eda Cengiz

Journal of Diabetes Science and Technology, Год журнала: 2024, Номер unknown

Опубликована: Дек. 31, 2024

Type 1 diabetes (T1D) necessitates lifelong insulin therapy due to the autoimmune destruction of insulin-producing pancreatic beta cells. Despite advancements in technology and formulations, maintaining optimal glycemic outcomes remains challenging these individuals. Obesity, accompanied by resistance, is common not only type 2 (T2D) but also many individuals with T1D. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), approved for T2D obesity, are now being explored off-label use This review examines their efficacy, safety, potential benefits T1D management. We reviewed articles published up May 2024 from databases like PubMed Scopus, mainly focusing on human studies GLP-1 RAs T1D, as well cardiorenal metabolic obesity. Semaglutide other showed significant improvements outcomes, hemoglobin A1c levels, reduced doses, notable weight loss. Studies obesity lipid profile offered protection. Common side effects include gastrointestinal issues, while some reported hypoglycemia, hyperglycemia, ketosis, others did not. challenges, offer therapeutic benefits, making them a promising adjunct improving clinical

Язык: Английский

Suicide and Self-Harm Events With GLP-1 Receptor Agonists in Adults With Diabetes or Obesity DOI
Pouya Ebrahimi, Juan C. Batlle, Aryan Ayati

и другие.

JAMA Psychiatry, Год журнала: 2025, Номер unknown

Опубликована: Март 19, 2025

Importance Bariatric surgery, once the criterion standard in obesity treatment, has a small but concerning association with increased suicidality. Glucagon-like peptide 1 receptor agonists (GLP-1 RAs), originally developed to treat diabetes, now provide substantial efficacy treatment of obesity. However, concerns risk suicidality these medicines have been raised. Objective To evaluate and self-harm randomized, placebo-controlled trials GLP-1 RAs adults diabetes or Data Sources MEDLINE, Embase, ClinicalTrials.gov, Cochrane databases were systematically searched from inception August 29, 2023. Study Selection Reports randomized clinical (RCTs) lasting 6 more months comparing placebo for published peer-reviewed journals identified. Two independent reviewers screened all search-identified studies inclusion. Records outcomes queried primary papers, ClinicalTrials.gov entries, corresponding authors. Extraction Synthesis researchers abstracted data assessed quality validity using PRISMA guidelines. pooled random-effects models. Main Outcomes Measures Pooled incidence completed attempted suicide, occurrences suicidal ideation, self-harm. Results A total 27 144 RCTs meeting inclusion criteria recorded suicide and/or self-harm-related events included 32 357 individuals receiving 046 treated placebo, over 74 740 68 095 person-years follow-up, respectively. Event was very low RA (0.044 per 100 person-years) (0.040 groups, no statistically significant difference (rate ratio [RR], 0.76; 95% CI, 0.48-1.21; P = .24). Subgroup analyses did not suggest differences based on status used. Five considered at bias due loss than 5% participants follow-up. Otherwise, found be heterogeneous nor high bias. Conclusions Relevance There is unlikely an increase suicide-related adverse among within context RCTs. While findings may further ease about effects, continued monitoring warranted identify particular patients who as extended use expands.

Язык: Английский

Процитировано

0

GLP-1 receptor agonists efficacy in managing comorbidities associated with diabetes mellitus: a narrative review DOI
Mahdi Gholami,

Narges Zargar Balajam,

Samira Rakhsha

и другие.

Journal of Diabetes & Metabolic Disorders, Год журнала: 2025, Номер 24(1)

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

La pagina gialla DOI
Sara Lega

Medico e Bambino, Год журнала: 2024, Номер 43(9), С. 553 - 554

Опубликована: Ноя. 7, 2024

Sipario: un dolce caso di fegato grande Indimenticabile! Osteomielite in pillole Terapia genica 1: virus che curano, uccidono 2: taglia e cuci Come vanno a finire Analoghi del GLP-1 salute mentale Good Morning AI!

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How to treat antipsychotic‐related weight gain and metabolic disturbances: Is there a role for GLP‐1 receptor agonists? DOI Open Access
Anders Fink‐Jensen, Christoph U. Correll

Acta Psychiatrica Scandinavica, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 8, 2024

Patients with mental disorders have a significantly reduced lifespan,1 overweight/obesity and cardiometabolic-related death being the biggest contributors. Both underlying illness treatments, especially antipsychotics, contribute to this increased cardiometabolic risk, creating dilemma between efficacy desired safety. As point in fact, clozapine is second-generation antipsychotic proven otherwise treatment-resistant patients diagnosis of schizophrenia. However, also linked substantial increase body weight carries high risk for metabolic disturbances,2 making clinicians, patients, caretakers reluctant against its use. Additionally, sedentary lifestyle unhealthy food intake become public health issue populations Western world general. they are an even bigger problem among people severe disorders, such as schizophrenia bipolar disorder. Also, use antipsychotics has expanded beyond disorder, used frequently on-label unipolar depression, but off-label impulsive behaviors, insomnia, anxiety other conditions.3 Over last decade, more focus been paid monitoring uncovering potential dysmetabolism by blood sample analysis treated which important steps right direction. clear, well-established strategies effective treatment and, especially, those receiving or mentally ill, remain underdeveloped or, at least, underutilized.4 The most strategy preventing antipsychotic-induced gain using these medications only when needed starting lowest potential.4 When adverse effects occur, secondary preventive efforts include switching less dysmetabolism, although loss may be limited.5 Moreover, case clozapine, partial complete antipsychotic, if it impose fewer dysmetabolic problems weight, not applicable strategy.6 Nonpharmacological interventions changes overweight well-known strategies7 but-as background population-are difficult implement broadly. Traditionally, adjunctive pharmacological antipsychotic-associated included topiramate metformin. weight-lowering compounds somewhat modest—typically range 3–4 kg over 12–24 weeks.8, 9 This leaves great need additional augmentation that mitigate, reverse, prevent antipsychotic-related gain, devoid any effects.10 Glucagon-like peptide-1 (GLP-1) incretin hormone synthesized L-cells intestine released response intake, causing delayed stomach emptying. GLP-1 receptor stimulation increases insulin secretion reduces glucagon secretion, thereby stabilizing glucose homeostasis.11 nucleus solitary tract brain stem hypothalamus areas involved satiety, where believed decrease appetite influence weight.12 agonists (GLP-1 RAs) clinic type 2 diabetes mellitus since 2007 2020, newer RAs, example, dulaglutide, semaglutide, tirzepatide, shown potent effects.13 To date, few studies investigated RAs specifically antipsychotic-treated data from incorporated recent systematic review meta-analysis Bak et al. showing beneficial on overweight.14 What risks psychiatric diagnosis? common events were nausea, vomiting, diarrhea generally tolerable14 similar trials. due preclinical evidence interact homeostasis, reducing dopamine caused drugs abuse,15 concern raised whether could induce anhedonia, suicidal ideation, worsen symptoms preexisting issues. Recent cohort studies16 post hoc clinical trials17 do indicate risk. general population trials, known illnesses excluded. Therefore, trials including essential ensure safe populations. In reviewed al., psychopathology was assessed different rating scales. transformed into one single scale: 7-point Clinical Global Impression Severity scale (CGI), no significant global observed.14 approach clearly lacks precision, number participants across four very small, mean identify individual who suicidal. further fully assess illness. Why commonly psychiatry? One argument abnormalities needed. Fortunately, several investigating RA finished recruitment (ClinicalTrials.gov ID NCT05333003; ClinicalTrials.gov NCT05193578). Hence, specific patient expected available soon. hope pharmaceutical companies would initiate larger RCTs populations, schizophrenia, depression prescribed particularly vulnerable burden. already approved diabetes, obesity factors, independent medication treatment, indication subgroup provide sufficient incentive, justify widespread prevention initiating relevant Another costs GLP-1RAs present, carry barriers equity issues non-psychiatric some patents expire soon, so cheaper RAS will likely cost preventable far higher. meantime, governments willing cover illness, treatment. AFJ received two unrestricted research grants Novo Nordisk A/S member advisory board study (no honorary). CUC consultant and/or advisor honoraria from: AbbVie, Alkermes, Allergan, Angelini, Aristo, Boehringer-Ingelheim, Bristol-Meyers Squibb, Cardio Diagnostics, Cerevel, CNX Therapeutics, Compass Pathways, Darnitsa, Delpor, Denovo, Eli Lilly, Gedeon Richter, Hikma, Holmusk, IntraCellular Therapies, Jamjoom Pharma, Janssen/J&J, Karuna, LB Lundbeck, MedInCell, MedLink, Merck, Mindpax, Mitsubishi Tanabe Maplight, Mylan, Neumora Neurocrine, Neurelis, Newron, Noven, Nordisk, Otsuka, PPD Biotech, Recordati, Relmada, Reviva, Rovi, Saladax, Sanofi, Seqirus, Servier, Sumitomo Pharma America, Sunovion, Sun Supernus, Tabuk, Takeda, Teva, Terran, Tolmar, Vertex, Viatris, Xenon Pharmaceuticals. He provided expert testimony Janssen, Otsuka. served Data Safety Monitoring Board Rovi. grant support Takeda. royalties UpToDate stock option holder Kuleon Biosciences, Medlink, Quantic, Terran. peer history article https://www.webofscience.com/api/gateway/wos/peer-review/10.1111/acps.13769.

Язык: Английский

Процитировано

0

Efficacy and Safety of Glp1-Ras Compared to Sglt2is and Dpp-4is in Individuals with Schizophrenia and Diabetes: A Danish Nationwide Target-Trial Emulation Study DOI

Søren Lundorff Jacobsen,

Ole Köhler‐Forsberg, Andreas Aalkjær Danielsen

и другие.

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

0

Suicide and suicide attempt in users of GLP-1 receptor agonists: a nationwide case-time-control study DOI Creative Commons
Julien Bezin, Anne Bénard‐Laribière,

Emilie Hucteau

и другие.

EClinicalMedicine, Год журнала: 2024, Номер 80, С. 103029 - 103029

Опубликована: Дек. 31, 2024

Язык: Английский

Процитировано

0

The Promise of Adjunct Medications in Improving Type 1 Diabetes Outcomes: Glucagon-like Peptide Receptor Agonists DOI Creative Commons
Sujatha Seetharaman, Eda Cengiz

Journal of Diabetes Science and Technology, Год журнала: 2024, Номер unknown

Опубликована: Дек. 31, 2024

Type 1 diabetes (T1D) necessitates lifelong insulin therapy due to the autoimmune destruction of insulin-producing pancreatic beta cells. Despite advancements in technology and formulations, maintaining optimal glycemic outcomes remains challenging these individuals. Obesity, accompanied by resistance, is common not only type 2 (T2D) but also many individuals with T1D. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), approved for T2D obesity, are now being explored off-label use This review examines their efficacy, safety, potential benefits T1D management. We reviewed articles published up May 2024 from databases like PubMed Scopus, mainly focusing on human studies GLP-1 RAs T1D, as well cardiorenal metabolic obesity. Semaglutide other showed significant improvements outcomes, hemoglobin A1c levels, reduced doses, notable weight loss. Studies obesity lipid profile offered protection. Common side effects include gastrointestinal issues, while some reported hypoglycemia, hyperglycemia, ketosis, others did not. challenges, offer therapeutic benefits, making them a promising adjunct improving clinical

Язык: Английский

Процитировано

0