Final answer:
Sulfa drugs are dangerous for patients with G6PD deficiency because they increase oxidative stress, leading to hemolytic anemia. These drugs inhibit bacterial folic acid synthesis, which can exacerbate conditions in susceptible individuals with genetic or metabolic disorders.
Step-by-step explanation:
Sulfa drugs are particularly dangerous for patients with the genetic disorder Glucose-6-phosphate dehydrogenase deficiency (G6PD). This condition impairs the body's ability to handle oxidative stress, which can be exacerbated by sulfonamides, potentially leading to a hemolytic anemia where red blood cells break down prematurely.
Sulfa drugs work by inhibiting the synthesis of folic acid in bacteria, which is necessary for nucleic acid synthesis and, thereby, cell division. This mechanism does not typically affect humans directly, since we obtain folic acid from our diet, but individuals with G6PD deficiency can experience severe side effects due to their underlying metabolic disorder.
Despite their usefulness in treating bacterial infections, taking sulfa drugs can lead to a deficiency in folic acid because these medications competitively inhibit the synthesis of folic acid by many types of microorganisms. Symptoms of such a deficiency include megablastic anemia, glossitis, gastrointestinal tract disturbances, and leucopenia. It is, therefore, important to prescribe them with caution to patients with certain genetic disorders or metabolic susceptibilities.