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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)...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
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.
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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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