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1.
J Drugs Dermatol ; 23(6): e144-e148, 2024 Jun 01.
Article En | MEDLINE | ID: mdl-38834228

Bullous pemphigoid is often difficult to treat with the limited therapies available. Here, we describe clinical outcomes among 30 adults with bullous pemphigoid patients treated with dupilumab. We performed a multicenter, retrospective case series between March 2020 to August 2022. Patients received a loading dose of dupilumab 600 mg, followed by 300 mg maintenance dose with varying administration frequency tailored to individual patient response. All patients experienced at least some improvement in blister formation and pruritus, with 23 (76.7%) of patients demonstrating either complete clearance of blistering or marked response. Complete clearance of pruritus or marked response was noted in 25 (83.3%) of patients. Eight patients were effectively maintained solely on dupilumab. One (3.3%) patient reported an injection site reaction. Thirty patients represent a small sample, however, to our knowledge, this is the second largest group of BP treated with dupilumab. Furthermore, we provide an understandable framework for clinicians outside of academics to follow and assess treatment responses in their BP patients treated with dupilumab. Dupilumab should be considered as a therapeutic option in patients with bullous pemphigoid given its ability to induce sustained blistering and pruritus response in both typical and refractory cases while maintaining a favorable safety profile. J Drugs Dermatol. 2024;23(6):e144-e148. doi:10.36849/JDD.8258e.


Antibodies, Monoclonal, Humanized , Pemphigoid, Bullous , Pruritus , Humans , Pemphigoid, Bullous/drug therapy , Pemphigoid, Bullous/diagnosis , Antibodies, Monoclonal, Humanized/administration & dosage , Antibodies, Monoclonal, Humanized/adverse effects , Antibodies, Monoclonal, Humanized/therapeutic use , Retrospective Studies , Female , Male , Aged , Middle Aged , Treatment Outcome , Aged, 80 and over , Pruritus/drug therapy , Pruritus/etiology , Pruritus/diagnosis , Adult , Injection Site Reaction/etiology , Injection Site Reaction/diagnosis
2.
Nutrients ; 15(19)2023 Sep 30.
Article En | MEDLINE | ID: mdl-37836507

Hypertension is the leading preventable risk factor for cardiovascular disease and all-cause mortality worldwide. However, studies have shown increased risk of mortality from heart disease and stroke even within the normal blood pressure (BP) range, starting at BPs above 110-115/70-75 mm Hg. Nutraceuticals, such as vitamins and minerals, have been studied extensively for their efficacy in lowering BP and may be of benefit to the general, normotensive population in achieving optimal BP. Our study investigated the effects of six nutraceuticals (Vitamins: C, D, E; Minerals: Calcium, Magnesium, Potassium) on both systolic blood pressure (SBP) and diastolic blood pressure (DBP) in this population. We performed a systematic review and pairwise meta-analysis for all six supplements versus placebo. Calcium and magnesium achieved significant reductions in both SBP and DBP of -1.37/-1.63 mm Hg and -2.79/-1.56 mm Hg, respectively. Vitamin E and potassium only yielded significant reductions in SBP with values of -1.76 mm Hg and -2.10 mm Hg, respectively. Vitamins C and D were not found to significantly lower either SBP or DBP. Future studies should determine optimal dosage and treatment length for these supplements in the general, normotensive population.


Hypertension , Hypotension , Humans , Vitamins , Blood Pressure , Magnesium/pharmacology , Magnesium/therapeutic use , Calcium/pharmacology , Dietary Supplements , Hypertension/epidemiology , Minerals/pharmacology , Minerals/therapeutic use , Hypotension/drug therapy , Calcium, Dietary/pharmacology , Potassium/pharmacology , Antihypertensive Agents/pharmacology
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