What is the major difference between the Somogyi effect and the dawn phenomenon?
One occurs between 4 a.m. and 9 a.m.
One is caused by the release of certain hormones.
One is characterized by hyperglycemia that is not triggered by overnight hypoglycemia.
One triggers insulin resistance and the release of glucose from the liver
The Correct Answer is C
Choice A reason: Both the Somogyi effect and the dawn phenomenon can occur between 4 a.m. and 9 a.m., so this is not a distinguishing factor between the two. They both involve changes in blood glucose levels during this early morning period.
Choice B reason: Both phenomena are influenced by the release of certain hormones, including growth hormone, cortisol, and catecholamines. These hormones can contribute to early morning hyperglycemia, but this alone does not differentiate the Somogyi effect from the dawn phenomenon.
Choice C reason: The Somogyi effect, also known as rebound hyperglycemia, is characterized by a period of hypoglycemia (low blood sugar) that occurs during the night, often as a result of excess insulin or other diabetic treatments. This overnight hypoglycemia triggers a counter-regulatory hormone response that leads to hyperglycemia in the early morning. In contrast, the dawn phenomenon is characterized by hyperglycemia in the early morning without preceding hypoglycemia. The dawn phenomenon is due to the natural overnight release of hormones like growth hormone and cortisol, which cause the liver to release glucose into the blood.
Choice D reason: While both effects involve hormone-mediated changes in glucose metabolism, the key difference lies in the presence or absence of preceding hypoglycemia. The dawn phenomenon does not involve insulin resistance triggered by overnight hypoglycemia, whereas the Somogyi effect does. The distinction primarily lies in the nocturnal blood sugar patterns and the body's response to them.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
Choice A reason: Type 1 diabetes cannot be treated with oral glycemic agents. These medications are typically used to manage type 2 diabetes, which is characterized by insulin resistance rather than a lack of insulin production. In type 1 diabetes, the pancreas is unable to produce insulin due to an autoimmune destruction of insulin-producing beta cells. Therefore, individuals with type 1 diabetes require insulin therapy to manage their blood glucose levels effectively.
Choice B reason: Type 1 diabetes has a definite genetic component, though it is not solely determined by genetics. A combination of genetic predisposition and environmental factors, such as viral infections or other autoimmune triggers, can lead to the development of type 1 diabetes. Certain genes, including those in the HLA region, are known to increase susceptibility to the disease.
Choice C reason: In type 1 diabetes, the pancreas is indeed completely unable to produce insulin. This is due to an autoimmune attack on the beta cells of the pancreas, which are responsible for insulin production. Without insulin, the body cannot regulate blood glucose levels, leading to hyperglycemia and the need for exogenous insulin administration.
Choice D reason: Type 1 diabetes often has an acute onset, particularly in children and young adults. Symptoms can develop rapidly over a few days to weeks, including increased thirst, frequent urination, unintended weight loss, and severe fatigue. This acute presentation is a hallmark of the disease and contrasts with the more gradual onset seen in type 2 diabetes.
Correct Answer is A
Explanation
Choice A reason: The primary distinction between ALL and AML is the type of cell that becomes cancerous. Acute Lymphocytic Leukemia (ALL) affects the lymphoid cell line. Lymphoid cells, or lymphocytes, are a type of white blood cell that plays a crucial role in the immune system, helping the body to fight infections. There are three types of lymphocytes: B cells, T cells, and natural killer (NK) cells. In ALL, the malignant transformation of these lymphocytes occurs, leading to an overproduction of immature lymphoid cells, or lymphoblasts. These lymphoblasts crowd out normal blood cells in the bone marrow, leading to symptoms such as anemia, susceptibility to infections, and easy bruising or bleeding.
Choice B reason: While it is true that ALL is more prevalent in children and AML is more common in adults, this age distribution is not the primary distinguishing feature between the two types of leukemia. ALL represents about 75% of pediatric leukemia cases, typically affecting children between 2 and 5 years old, while AML is more commonly diagnosed in adults, with the incidence increasing with age. However, both types can occur at any age, and the age of onset alone is not sufficient to distinguish between them. The differentiation based on cell type remains the most significant factor.
Choice C reason: Clinical manifestations of ALL and AML can be very similar because both involve the proliferation of immature white blood cells in the bone marrow, which disrupts normal blood cell production. Common symptoms include fatigue, frequent infections, fever, weight loss, easy bruising or bleeding, and bone pain. These symptoms result from the overproduction of immature leukemic cells and the subsequent suppression of normal hematopoiesis. Although there may be some differences in presentation based on the specific cell types involved, clinical manifestations are not the primary basis for differentiating between ALL and AML.
Choice D reason: The diagnostic tests used for ALL and AML are quite similar and typically include complete blood counts (CBC), bone marrow biopsy, and flow cytometry to identify the types of cells involved. Cytogenetic and molecular studies are also used to detect specific genetic abnormalities associated with each type of leukemia. While certain markers and genetic mutations may differ between ALL and AML, the overall approach to diagnosis involves similar testing methods. Therefore, the primary difference between the two leukemias lies in the cell type affected rather than the specific diagnostic tests used.
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