Behavioral Sciences in the Optimization of Pharmacological and Non-Pharmacological Therapy for Type 2 Diabetes
Abstract
:1. Introduction
Country | No. of Studies | Prevalence | Country | No. of Studies | Prevalence |
---|---|---|---|---|---|
Belgium | 1 | 16.6% | South Africa | 2 | 5.8% |
Canada | 1 | 14.8% | France | 1 | 5.6% |
USA | 3 | 13.0% | Greece | 1 | 4.8% |
Trinidad | 1 | 12.2% | Jordan | 2 | 4.2% |
India | 2 | 11.6% | China | 10 | 4.1% |
Norway | 1 | 10.4% | Uganda | 1 | 4.0% |
Cameroon | 3 | 9.9% | Ireland | 1 | 3.9% |
Italy | 1 | 9.7% | Turkey | 1 | 3.1% |
Thailand | 2 | 8.8% | Spain | 5 | 3.0% |
Denmark | 1 | 7.8% | Germany | 2 | 2.8% |
Pakistan | 4 | 7.4% | Saudi Arabia | 1 | 2.3% |
Tanzania | 2 | 7.3% | Japan | 1 | 2.0% |
Pacific island countries | 1 | 6.8% | Netherlands | 2 | 1.8% |
United Kingdom | 4 | 6.3% | Korea | 2 | 1.7% |
Egypt | 2 | 6% | Poland | 1 | 1.7% |
Bahrain | 1 | 5.9% | Australia | 2 | 1.5% |
2. Materials and Methods
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- The guiding principle used in this review, which, in the end, defines the central issue of this work, is the importance of behavioral sciences in the perspective of prevention, treatment and adequate control of DM2, so the adoption of assertive behaviors assumes an extreme preponderance in achieving positive results, with health professionals having a decisive role in defining effective strategies to ensure that patients can assume a commitment, at a behavioral level, leading to the success of pharmacological and non-pharmacological treatments instituted.
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- This narrative review intends to contextualize the disease from a historical point of view; summarize the essence of behavioral sciences and what is its framework; discuss what kind of approach should be taken both in terms of lifestyle and pharmacologically, given the pathophysiology of DM2, reviewing the therapeutic options currently available and its main characteristics that can influence the behavior of patients; and address the potentially modifiable aspects that are decisive in influencing the behavior of patients with DM2.
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- The main sources of information were databases such as PubMed, IDF Diabetes Atlas, the Portuguese Society of Diabetology, as well as manuals in the field of Pharmacology/Pharmacotherapy, focusing generically on search terms such as behavioral sciences, history, pathophysiology, lifestyle and complications/comorbidities in diabetes, and specifically guidelines for the treatment of DM2 and behavioral sciences in diabetes.
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- The key statements are supported by references to studies carried out in the past 30 years in the field of behavioral sciences as well as on the history, incidence, pathophysiology and drug therapy of DM2. We used a three-stage approach to review the literature:
- The first stage consisted of researching statistical information about the disease in terms of its prevalence.
- The second stage refers to the research of articles and bibliography in a historical and social perspective of the disease; pathophysiology, lifestyle and pharmacology in the DM2.
- The third stage reports on research carried out in the area of behavioral sciences in general and in DM2 in particular.
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- The initial keywords were organized into the following conceptual categories: type 2 diabetes, behavioral sciences, lifestyle, self-control and antidiabetic therapy. Search terms were developed and customized for each database.
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- The data and information gathered are presented establishing a logical sequence that aims to demonstrate how it is possible to identify and act to ensure adequate control of DM2 from the behavioral perspective of patients with the disease.
3. Main Findings
3.1. Historical and Social Context of the Disease and Behaviors
3.2. The Essence of Behavioral Sciences
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- The number of variables involved is small and the dynamics can be significantly evaluated in just a few points of time;
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- The change process is the same for all individuals, e.g., following the same sequence;
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- The dynamics between variables is linear, additive and does not change over time; and
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- Included variables are not diluted in context or omitted.
3.3. Pathophysiology of Type 2 Diabetes
3.4. Healthy Lifestyle
- Lifestyle changes with the adoption of adequate eating habits and physical exercise throughout the course of the disease;
- Individualization of therapy and patient-centeredness; and
- Therapeutic Education (TE) or DSMES (Diabetes Self-Management Education and Support), which is essential in the care provided to people with type 2 diabetes.
3.5. Pharmacological Treatment
3.6. Potentially Modifiable Factors in Which Efforts Should Be Made to Influence the Behavior of Patients with DM2
3.6.1. The Effectiveness of the Treatment According to the Patient’s Perception
3.6.2. The Incidence of Hypoglycemia
3.6.3. Complexity and Convenience of Treatment
3.6.4. Costs of Treatment
3.6.5. Beliefs Regarding Medication
3.6.6. Trust in Health Professionals
4. Discussion
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Conflicts of Interest
References
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Drug | Mechanism of Action | Risk of Hypoglycemia | Weight | Secondary Effects |
---|---|---|---|---|
Metformin (*) | ↓ hepatic glucose synthesis | Not associated | ↓ | GI changes (diarrhea and vomiting) and vitamin B12 deficiency |
α-Glucosidase inhibitors (**) | Prevent the breakdown of complex carbohydrates in the small intestine, delaying their absorption | Not associated | = | Diarrhea, flatulence or abdominal discomfort |
Sodium-glucose cotransporter inhibitors (SGLT2) | ↑ elimination of glucose in the urine and block its renal absorption | Not associated | ↓ | ↑ risk of genitourinary infections, hypovolemia with hypotension, increased LDL cholesterol and may even lead to a transient increase in creatinine |
Glucagon-like peptide−1 agonists (GLP−1 agonists) | ↑ insulin secretion, by decreasing glucagon secretion, delaying gastric emptying, also promoting the feeling of satiety | Low | ↓ | Nausea, diarrhea, vomiting, and headache |
Dipeptidyl peptidase 4 inhibitors (iDPP4) | Inhibit the degradation of incretins which promote↑ secretion of insulin and the ↓ of glucagon secretion | Not associated | = | Well tolerated |
Thiazolidinediones | ↑ peripheral insulin sensitivity in liver, fat and skeletal muscle cells | Not associated | ↑ but ↓ visceral obesity | ↑ risk of fluid retention (edema), congestive heart failure and an increased risk of bone fractures |
Sulfonylureas and Glinides (***) | Secretagogues (↑ insulin secretion) | Increased risk | ↑ | Well tolerated |
Insulins (****) | Activates insulin receptors | High | ↑ | Possibility of local allergic reactions |
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Lopes, A.; Roque, F.; Morgado, S.; Dinis, C.; Herdeiro, M.T.; Morgado, M. Behavioral Sciences in the Optimization of Pharmacological and Non-Pharmacological Therapy for Type 2 Diabetes. Behav. Sci. 2021, 11, 153. https://doi.org/10.3390/bs11110153
Lopes A, Roque F, Morgado S, Dinis C, Herdeiro MT, Morgado M. Behavioral Sciences in the Optimization of Pharmacological and Non-Pharmacological Therapy for Type 2 Diabetes. Behavioral Sciences. 2021; 11(11):153. https://doi.org/10.3390/bs11110153
Chicago/Turabian StyleLopes, António, Fátima Roque, Sandra Morgado, Cristina Dinis, Maria Teresa Herdeiro, and Manuel Morgado. 2021. "Behavioral Sciences in the Optimization of Pharmacological and Non-Pharmacological Therapy for Type 2 Diabetes" Behavioral Sciences 11, no. 11: 153. https://doi.org/10.3390/bs11110153
APA StyleLopes, A., Roque, F., Morgado, S., Dinis, C., Herdeiro, M. T., & Morgado, M. (2021). Behavioral Sciences in the Optimization of Pharmacological and Non-Pharmacological Therapy for Type 2 Diabetes. Behavioral Sciences, 11(11), 153. https://doi.org/10.3390/bs11110153