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Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years

BACKGROUND: A retrospective review of clinical manifestations and demographic pattern of patients diagnosed as chronic granulomatous disease (CGD) from 7 hospitals in Malaysia. An analysis of the available database would establish clinical characteristics, diagnoses and outcome including microbiolog...

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Autores principales: Noh, Lokman Mohd, Latiff, Amir Hamzah Abdul, Ismail, Intan Hakimah, Noah, Rahim Md, Wahab, Asrul Abdul, Hamid, Intan Juliana Abd., Ripen, Adiratna Mat, Abdullah, Nasuruddin B., Razali, Kamarul Azhar, Zainudin, Norzila, Bakon, Florence, Kok, Long Juan, Ali, Adli, Aziz, Bilkis Banu SAbd, Latif, Hasniah Abdul, Mohamad, Siti Mardhiana, Zainudeen, Zarina Thasneem, Hashim, Ilie Fadzilah, Sendut, Iean Hamzah, Nadarajaw, Thiyagar, Jamil, Faizah Mohamed, Ng, David C. E., Abidin, Mohd Azri Zainal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130441/
https://www.ncbi.nlm.nih.gov/pubmed/34001231
http://dx.doi.org/10.1186/s13223-021-00551-4
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author Noh, Lokman Mohd
Latiff, Amir Hamzah Abdul
Ismail, Intan Hakimah
Noah, Rahim Md
Wahab, Asrul Abdul
Hamid, Intan Juliana Abd.
Ripen, Adiratna Mat
Abdullah, Nasuruddin B.
Razali, Kamarul Azhar
Zainudin, Norzila
Bakon, Florence
Kok, Long Juan
Ali, Adli
Aziz, Bilkis Banu SAbd
Latif, Hasniah Abdul
Mohamad, Siti Mardhiana
Zainudeen, Zarina Thasneem
Hashim, Ilie Fadzilah
Sendut, Iean Hamzah
Nadarajaw, Thiyagar
Jamil, Faizah Mohamed
Ng, David C. E.
Abidin, Mohd Azri Zainal
author_facet Noh, Lokman Mohd
Latiff, Amir Hamzah Abdul
Ismail, Intan Hakimah
Noah, Rahim Md
Wahab, Asrul Abdul
Hamid, Intan Juliana Abd.
Ripen, Adiratna Mat
Abdullah, Nasuruddin B.
Razali, Kamarul Azhar
Zainudin, Norzila
Bakon, Florence
Kok, Long Juan
Ali, Adli
Aziz, Bilkis Banu SAbd
Latif, Hasniah Abdul
Mohamad, Siti Mardhiana
Zainudeen, Zarina Thasneem
Hashim, Ilie Fadzilah
Sendut, Iean Hamzah
Nadarajaw, Thiyagar
Jamil, Faizah Mohamed
Ng, David C. E.
Abidin, Mohd Azri Zainal
author_sort Noh, Lokman Mohd
collection PubMed
description BACKGROUND: A retrospective review of clinical manifestations and demographic pattern of patients diagnosed as chronic granulomatous disease (CGD) from 7 hospitals in Malaysia. An analysis of the available database would establish clinical characteristics, diagnoses and outcome including microbiologic pattern. Studying the demography allows us to document the occurrence of CGD amongst multiethnic groups and its geographical distribution for Malaysia. METHODS: Data from the Malaysia Primary Immunodeficiency Network (MyPIN) with cases of CGD diagnosed from 1991 until 2016 were collated and analysed. RESULTS: Twenty patients were diagnosed as CGD. Males (N = 13, 65%) outnumber females (N = 7, 35%). CGD is commonest amongst the Malays (65%) followed by the Chinese (15.0%), Indians (10.0%) and natives of Borneo (10.0%), reflecting the ethnic composition of the country. The mean age of diagnosis was 3.7 years. There was a positive family history in 40% of the cases. Abscess was the main presenting feature in 16 patients (80%) with one involving the brain. Pneumonia occurred in 10 (50%) and one with complicated bronchiectasis. Catalase-positive bacteria were the most commonly isolated pathogen with Chromobacterium violaceum predominating (N = 5, 25%) with consequent high mortality (N = 4, 80%). All CGD patients with C. violaceum infection displayed CD4 + (T helper cells) lymphopenia. CONCLUSION: This study has shown CGD occurs in the major ethnic groups of Malaysia. To the best of our knowledge, this is the first and the largest series of chronic granulomatous disease in South East Asia which may be reflective of similar clinical pattern in the region. C. violaceum infection is associated with a higher mortality in CGD patients in Malaysia. All the CGD patients with C. violaceum infection in this patient series displayed CD4 + (T helper) lymphopenia. We recorded rare clinical manifestation of CGD viz. brain abscess and bronchiectasis.
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spelling pubmed-81304412021-05-19 Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years Noh, Lokman Mohd Latiff, Amir Hamzah Abdul Ismail, Intan Hakimah Noah, Rahim Md Wahab, Asrul Abdul Hamid, Intan Juliana Abd. Ripen, Adiratna Mat Abdullah, Nasuruddin B. Razali, Kamarul Azhar Zainudin, Norzila Bakon, Florence Kok, Long Juan Ali, Adli Aziz, Bilkis Banu SAbd Latif, Hasniah Abdul Mohamad, Siti Mardhiana Zainudeen, Zarina Thasneem Hashim, Ilie Fadzilah Sendut, Iean Hamzah Nadarajaw, Thiyagar Jamil, Faizah Mohamed Ng, David C. E. Abidin, Mohd Azri Zainal Allergy Asthma Clin Immunol Research BACKGROUND: A retrospective review of clinical manifestations and demographic pattern of patients diagnosed as chronic granulomatous disease (CGD) from 7 hospitals in Malaysia. An analysis of the available database would establish clinical characteristics, diagnoses and outcome including microbiologic pattern. Studying the demography allows us to document the occurrence of CGD amongst multiethnic groups and its geographical distribution for Malaysia. METHODS: Data from the Malaysia Primary Immunodeficiency Network (MyPIN) with cases of CGD diagnosed from 1991 until 2016 were collated and analysed. RESULTS: Twenty patients were diagnosed as CGD. Males (N = 13, 65%) outnumber females (N = 7, 35%). CGD is commonest amongst the Malays (65%) followed by the Chinese (15.0%), Indians (10.0%) and natives of Borneo (10.0%), reflecting the ethnic composition of the country. The mean age of diagnosis was 3.7 years. There was a positive family history in 40% of the cases. Abscess was the main presenting feature in 16 patients (80%) with one involving the brain. Pneumonia occurred in 10 (50%) and one with complicated bronchiectasis. Catalase-positive bacteria were the most commonly isolated pathogen with Chromobacterium violaceum predominating (N = 5, 25%) with consequent high mortality (N = 4, 80%). All CGD patients with C. violaceum infection displayed CD4 + (T helper cells) lymphopenia. CONCLUSION: This study has shown CGD occurs in the major ethnic groups of Malaysia. To the best of our knowledge, this is the first and the largest series of chronic granulomatous disease in South East Asia which may be reflective of similar clinical pattern in the region. C. violaceum infection is associated with a higher mortality in CGD patients in Malaysia. All the CGD patients with C. violaceum infection in this patient series displayed CD4 + (T helper) lymphopenia. We recorded rare clinical manifestation of CGD viz. brain abscess and bronchiectasis. BioMed Central 2021-05-17 /pmc/articles/PMC8130441/ /pubmed/34001231 http://dx.doi.org/10.1186/s13223-021-00551-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Noh, Lokman Mohd
Latiff, Amir Hamzah Abdul
Ismail, Intan Hakimah
Noah, Rahim Md
Wahab, Asrul Abdul
Hamid, Intan Juliana Abd.
Ripen, Adiratna Mat
Abdullah, Nasuruddin B.
Razali, Kamarul Azhar
Zainudin, Norzila
Bakon, Florence
Kok, Long Juan
Ali, Adli
Aziz, Bilkis Banu SAbd
Latif, Hasniah Abdul
Mohamad, Siti Mardhiana
Zainudeen, Zarina Thasneem
Hashim, Ilie Fadzilah
Sendut, Iean Hamzah
Nadarajaw, Thiyagar
Jamil, Faizah Mohamed
Ng, David C. E.
Abidin, Mohd Azri Zainal
Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title_full Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title_fullStr Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title_full_unstemmed Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title_short Clinical and demographic pattern of chronic granulomatous disease (CGD) from a multicenter perspective: Malaysia’s experience over 26 years
title_sort clinical and demographic pattern of chronic granulomatous disease (cgd) from a multicenter perspective: malaysia’s experience over 26 years
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130441/
https://www.ncbi.nlm.nih.gov/pubmed/34001231
http://dx.doi.org/10.1186/s13223-021-00551-4
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