Ewa Ternesten-Hasséus PhD , Ewa-Lena Johansson PhD , Eva Millqvist MD, PhD
{"title":"口服辣椒素治疗不明原因的慢性咳嗽和气道症状","authors":"Ewa Ternesten-Hasséus PhD , Ewa-Lena Johansson PhD , Eva Millqvist MD, PhD","doi":"10.1016/j.chpulm.2024.100049","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Unexplained chronic cough (UCC) is characterized by persistent coughing without evident medical explanation.</p></div><div><h3>Research Question</h3><p>Does daily oral administration of natural capsaicin (chili) improve refractory coughing in patients with UCC?</p></div><div><h3>Study Design and Methods</h3><p>Forty-six patients (mean age, 60.5 years) with UCC participated in this crossover, randomized double-anonymized study. For 4 weeks, the participants took capsules containing pure capsaicin orally, and after a washout of 2 weeks, took placebo capsules for 4 weeks. A capsaicin inhalation cough test was used to assess the capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs. The number of coughs in a 24-h period and the number of coughs per hour were recorded on four occasions using the Leicester Cough Monitor. Participants completed questionnaires with items on cough, cough-related symptoms, and quality of life.</p></div><div><h3>Results</h3><p>The mean values for capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs increased after the capsaicin treatment period as compared with the first visit (baseline; <em>P</em> < .05 and <em>P</em> < .03, respectively), although they did not differ from the placebo recordings. Neither the capsaicin nor the placebo treatment significantly reduced the cough frequency, nor did they differ between the two treatment periods. When dividing the participants into low-cougher (≤ 400 coughs within 24 h) and high-cougher (> 400 coughs within 24 h) groups, the low coughers experienced a significantly better outcome from capsaicin, but not from placebo. The visual analog scale symptom scores improved after capsaicin treatment compared with baseline and placebo treatment in terms of the frequencies of coughing (<em>P < .</em>001), rhinitis (<em>P < .</em>03), and throat irritation (<em>P < .</em>01). The Leicester Cough Questionnaire scores improved after capsaicin treatment compared with baseline and compared with the placebo treatment group for all the domains (<em>P < .</em>01 for the total score).</p></div><div><h3>Interpretation</h3><p>In this study, capsaicin powder taken orally was found to be clinically effective and well tolerated by patients with UCC. The results suggest a future treatment for UCC.</p></div><div><h3>Trial Registry</h3><p>European Union Drug Regulating Authorities Clinical Trials Database; No.: EudraCT 2016-004463-39; URL: <span>https://www.clinicaltrialsregister.eu</span><svg><path></path></svg></p><p>ClinicalTrials.gov; No.: <span>NCT04125563</span><svg><path></path></svg>; URL: <span>www.clinicaltrials.gov</span><svg><path></path></svg></p></div>","PeriodicalId":94286,"journal":{"name":"CHEST pulmonary","volume":"2 3","pages":"Article 100049"},"PeriodicalIF":0.0000,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949789224000151/pdfft?md5=38d3d9b768ac0c1e7fe04c5fc22f885b&pid=1-s2.0-S2949789224000151-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Oral Capsaicin as Treatment for Unexplained Chronic Cough and Airway Symptoms\",\"authors\":\"Ewa Ternesten-Hasséus PhD , Ewa-Lena Johansson PhD , Eva Millqvist MD, PhD\",\"doi\":\"10.1016/j.chpulm.2024.100049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Unexplained chronic cough (UCC) is characterized by persistent coughing without evident medical explanation.</p></div><div><h3>Research Question</h3><p>Does daily oral administration of natural capsaicin (chili) improve refractory coughing in patients with UCC?</p></div><div><h3>Study Design and Methods</h3><p>Forty-six patients (mean age, 60.5 years) with UCC participated in this crossover, randomized double-anonymized study. For 4 weeks, the participants took capsules containing pure capsaicin orally, and after a washout of 2 weeks, took placebo capsules for 4 weeks. A capsaicin inhalation cough test was used to assess the capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs. The number of coughs in a 24-h period and the number of coughs per hour were recorded on four occasions using the Leicester Cough Monitor. Participants completed questionnaires with items on cough, cough-related symptoms, and quality of life.</p></div><div><h3>Results</h3><p>The mean values for capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs increased after the capsaicin treatment period as compared with the first visit (baseline; <em>P</em> < .05 and <em>P</em> < .03, respectively), although they did not differ from the placebo recordings. Neither the capsaicin nor the placebo treatment significantly reduced the cough frequency, nor did they differ between the two treatment periods. When dividing the participants into low-cougher (≤ 400 coughs within 24 h) and high-cougher (> 400 coughs within 24 h) groups, the low coughers experienced a significantly better outcome from capsaicin, but not from placebo. The visual analog scale symptom scores improved after capsaicin treatment compared with baseline and placebo treatment in terms of the frequencies of coughing (<em>P < .</em>001), rhinitis (<em>P < .</em>03), and throat irritation (<em>P < .</em>01). The Leicester Cough Questionnaire scores improved after capsaicin treatment compared with baseline and compared with the placebo treatment group for all the domains (<em>P < .</em>01 for the total score).</p></div><div><h3>Interpretation</h3><p>In this study, capsaicin powder taken orally was found to be clinically effective and well tolerated by patients with UCC. The results suggest a future treatment for UCC.</p></div><div><h3>Trial Registry</h3><p>European Union Drug Regulating Authorities Clinical Trials Database; No.: EudraCT 2016-004463-39; URL: <span>https://www.clinicaltrialsregister.eu</span><svg><path></path></svg></p><p>ClinicalTrials.gov; No.: <span>NCT04125563</span><svg><path></path></svg>; URL: <span>www.clinicaltrials.gov</span><svg><path></path></svg></p></div>\",\"PeriodicalId\":94286,\"journal\":{\"name\":\"CHEST pulmonary\",\"volume\":\"2 3\",\"pages\":\"Article 100049\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-03-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2949789224000151/pdfft?md5=38d3d9b768ac0c1e7fe04c5fc22f885b&pid=1-s2.0-S2949789224000151-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CHEST pulmonary\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949789224000151\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CHEST pulmonary","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949789224000151","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Oral Capsaicin as Treatment for Unexplained Chronic Cough and Airway Symptoms
Background
Unexplained chronic cough (UCC) is characterized by persistent coughing without evident medical explanation.
Research Question
Does daily oral administration of natural capsaicin (chili) improve refractory coughing in patients with UCC?
Study Design and Methods
Forty-six patients (mean age, 60.5 years) with UCC participated in this crossover, randomized double-anonymized study. For 4 weeks, the participants took capsules containing pure capsaicin orally, and after a washout of 2 weeks, took placebo capsules for 4 weeks. A capsaicin inhalation cough test was used to assess the capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs. The number of coughs in a 24-h period and the number of coughs per hour were recorded on four occasions using the Leicester Cough Monitor. Participants completed questionnaires with items on cough, cough-related symptoms, and quality of life.
Results
The mean values for capsaicin inhalation concentration required to reach two coughs and the capsaicin inhalation concentration required to reach five coughs increased after the capsaicin treatment period as compared with the first visit (baseline; P < .05 and P < .03, respectively), although they did not differ from the placebo recordings. Neither the capsaicin nor the placebo treatment significantly reduced the cough frequency, nor did they differ between the two treatment periods. When dividing the participants into low-cougher (≤ 400 coughs within 24 h) and high-cougher (> 400 coughs within 24 h) groups, the low coughers experienced a significantly better outcome from capsaicin, but not from placebo. The visual analog scale symptom scores improved after capsaicin treatment compared with baseline and placebo treatment in terms of the frequencies of coughing (P < .001), rhinitis (P < .03), and throat irritation (P < .01). The Leicester Cough Questionnaire scores improved after capsaicin treatment compared with baseline and compared with the placebo treatment group for all the domains (P < .01 for the total score).
Interpretation
In this study, capsaicin powder taken orally was found to be clinically effective and well tolerated by patients with UCC. The results suggest a future treatment for UCC.
Trial Registry
European Union Drug Regulating Authorities Clinical Trials Database; No.: EudraCT 2016-004463-39; URL: https://www.clinicaltrialsregister.eu