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Intestinal alkaline phosphatase deficiency increases the risk of diabetes
INTRODUCTION: Our previous case–control study demonstrated that a high level of intestinal alkaline phosphatase (IAP), an endotoxin-detoxifying anti-inflammatory enzyme secreted by villus-associated enterocytes and excreted with stool, plays a protective role against type 2 diabetes mellitus (T2DM)...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796214/ https://www.ncbi.nlm.nih.gov/pubmed/35082135 http://dx.doi.org/10.1136/bmjdrc-2021-002643 |
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author | Malo, Jagannath Alam, Md Jahangir Islam, Salequl Mottalib, Md Abdul Rocki, Md Mehedi Hasan Barmon, Ginok Tinni, Shamema Akter Barman, Swapan K Sarker, Tapas Khan, Md Nayeemul Islam Kaliannan, Kanakaraju Hasanat, Muhammad Abul Rahman, Salimur Pathan, Md Faruque Khan, A K Azad Malo, Madhu S |
author_facet | Malo, Jagannath Alam, Md Jahangir Islam, Salequl Mottalib, Md Abdul Rocki, Md Mehedi Hasan Barmon, Ginok Tinni, Shamema Akter Barman, Swapan K Sarker, Tapas Khan, Md Nayeemul Islam Kaliannan, Kanakaraju Hasanat, Muhammad Abul Rahman, Salimur Pathan, Md Faruque Khan, A K Azad Malo, Madhu S |
author_sort | Malo, Jagannath |
collection | PubMed |
description | INTRODUCTION: Our previous case–control study demonstrated that a high level of intestinal alkaline phosphatase (IAP), an endotoxin-detoxifying anti-inflammatory enzyme secreted by villus-associated enterocytes and excreted with stool, plays a protective role against type 2 diabetes mellitus (T2DM) irrespective of obesity. In the current study, we investigated the long-term effect of IAP deficiency (IAPD) on the pathogenesis of T2DM. RESEARCH DESIGN AND METHODS: A healthy cohort of participants without diabetes (30–60 years old), comprising 188 without IAPD (IAP level: ≥65 U/g stool) and 386 with IAPD (IAP level: <65 U/g stool), were followed up for 5 years. We measured stool IAP (STAP) and fasting plasma glucose, and calculated the risk ratio (RR) using log-binomial regression model. RESULTS: T2DM incidence rates were 8.0%, 11.7%, 25.6%, and 33.3% in participants with ‘persistent no IAPD’ (IAP level: always ≥65 U/g stool), ‘remittent IAPD’ (IAP level: increased from <65 U/g stool to ≥65 U/g stool), ‘persistent IAPD’ (IAP level: always <65 U/g stool), and ‘incident IAPD’ (IAP level: decreased from ≥65 U/g stool to <65 U/g stool), respectively. Compared with ‘persistent no IAPD’ the risk of developing T2DM with ‘incident IAPD’ was 270% higher (RR: 3.69 (95% CI 1.76 to 7.71), χ(2) p<0.001). With ‘persistent IAPD’ the risk was 230% higher (RR: 3.27 (95% CI 1.64 to 6.50), p<0.001). ‘Remittent IAPD’ showed insignificant risk (RR: 2.24 (95% CI 0.99 to 5.11), p=0.0541). Sensitivity analyses of persistent IAP levels revealed that, compared with participants of the highest persistent IAP pentile (always >115 U/g stool), the rate of increase of fasting glycemia was double and the risk of developing T2DM was 1280% higher (RR: 13.80 (95% CI 1.87 to 101.3), p=0.0099) in participants of the lowest persistent IAP pentile (always <15 U/g stool). A diabetes pathogenesis model is presented. CONCLUSIONS: IAPD increases the risk of developing T2DM, and regular STAP tests would predict individual vulnerability to T2DM. Oral IAP supplementation might prevent T2DM. |
format | Online Article Text |
id | pubmed-8796214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-87962142022-02-07 Intestinal alkaline phosphatase deficiency increases the risk of diabetes Malo, Jagannath Alam, Md Jahangir Islam, Salequl Mottalib, Md Abdul Rocki, Md Mehedi Hasan Barmon, Ginok Tinni, Shamema Akter Barman, Swapan K Sarker, Tapas Khan, Md Nayeemul Islam Kaliannan, Kanakaraju Hasanat, Muhammad Abul Rahman, Salimur Pathan, Md Faruque Khan, A K Azad Malo, Madhu S BMJ Open Diabetes Res Care Epidemiology/Health services research INTRODUCTION: Our previous case–control study demonstrated that a high level of intestinal alkaline phosphatase (IAP), an endotoxin-detoxifying anti-inflammatory enzyme secreted by villus-associated enterocytes and excreted with stool, plays a protective role against type 2 diabetes mellitus (T2DM) irrespective of obesity. In the current study, we investigated the long-term effect of IAP deficiency (IAPD) on the pathogenesis of T2DM. RESEARCH DESIGN AND METHODS: A healthy cohort of participants without diabetes (30–60 years old), comprising 188 without IAPD (IAP level: ≥65 U/g stool) and 386 with IAPD (IAP level: <65 U/g stool), were followed up for 5 years. We measured stool IAP (STAP) and fasting plasma glucose, and calculated the risk ratio (RR) using log-binomial regression model. RESULTS: T2DM incidence rates were 8.0%, 11.7%, 25.6%, and 33.3% in participants with ‘persistent no IAPD’ (IAP level: always ≥65 U/g stool), ‘remittent IAPD’ (IAP level: increased from <65 U/g stool to ≥65 U/g stool), ‘persistent IAPD’ (IAP level: always <65 U/g stool), and ‘incident IAPD’ (IAP level: decreased from ≥65 U/g stool to <65 U/g stool), respectively. Compared with ‘persistent no IAPD’ the risk of developing T2DM with ‘incident IAPD’ was 270% higher (RR: 3.69 (95% CI 1.76 to 7.71), χ(2) p<0.001). With ‘persistent IAPD’ the risk was 230% higher (RR: 3.27 (95% CI 1.64 to 6.50), p<0.001). ‘Remittent IAPD’ showed insignificant risk (RR: 2.24 (95% CI 0.99 to 5.11), p=0.0541). Sensitivity analyses of persistent IAP levels revealed that, compared with participants of the highest persistent IAP pentile (always >115 U/g stool), the rate of increase of fasting glycemia was double and the risk of developing T2DM was 1280% higher (RR: 13.80 (95% CI 1.87 to 101.3), p=0.0099) in participants of the lowest persistent IAP pentile (always <15 U/g stool). A diabetes pathogenesis model is presented. CONCLUSIONS: IAPD increases the risk of developing T2DM, and regular STAP tests would predict individual vulnerability to T2DM. Oral IAP supplementation might prevent T2DM. BMJ Publishing Group 2022-01-26 /pmc/articles/PMC8796214/ /pubmed/35082135 http://dx.doi.org/10.1136/bmjdrc-2021-002643 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Epidemiology/Health services research Malo, Jagannath Alam, Md Jahangir Islam, Salequl Mottalib, Md Abdul Rocki, Md Mehedi Hasan Barmon, Ginok Tinni, Shamema Akter Barman, Swapan K Sarker, Tapas Khan, Md Nayeemul Islam Kaliannan, Kanakaraju Hasanat, Muhammad Abul Rahman, Salimur Pathan, Md Faruque Khan, A K Azad Malo, Madhu S Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title | Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title_full | Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title_fullStr | Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title_full_unstemmed | Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title_short | Intestinal alkaline phosphatase deficiency increases the risk of diabetes |
title_sort | intestinal alkaline phosphatase deficiency increases the risk of diabetes |
topic | Epidemiology/Health services research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796214/ https://www.ncbi.nlm.nih.gov/pubmed/35082135 http://dx.doi.org/10.1136/bmjdrc-2021-002643 |
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