The role of modulators in cystic fibrosis related diabetes
被引:26
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作者:
Merjaneh, Lina
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机构:
Seattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USASeattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USA
Merjaneh, Lina
[1
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Hasan, Sana
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机构:
Cleveland Clin Fdn, Dept Endocrinol & Metab, Cleveland, OH USASeattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USA
Hasan, Sana
[2
]
Kasim, Nader
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机构:
Helen Devos Childrens Hosp, Div Pediat Diabet & Endocrinol, Spectrum Hlth, Grand Rapids, MI USASeattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USA
Kasim, Nader
[3
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Ode, Katie Larson
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机构:
Univ Iowa, Dept Pediat, Div Endocrinol, Stead Family Childrens Hosp, Iowa City, IA USASeattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USA
Ode, Katie Larson
[4
]
机构:
[1] Seattle Childrens Hosp, Dept Pediat, Div Endocrinol, Seattle, WA USA
The development and introduction of modulator therapies have completely shifted the paradigm for the treatment of cystic fibrosis (CF). Highly effective modulator therapies have driven marked improvements in lung function, exacerbation rate, weight and quality of life in CF patients. However, their effect on CF related diabetes (CFRD) is not well delineated. The role of CF transmembrane conductance regulator (CFTR) in CFRD pathogenesis is inadequately understood and research aimed at deciphering the underlying mechanisms of CFRD continues to evolve. In this review, we summarize what is known regarding the effect of CFTR modulators on CFRD. Small studies using ivacaftor monotherapy in gating mutations have revealed improvement in insulin secretion, glucose tolerance and/or decrease in insulin requirement. However, lumacaftor/ivacaftor studies (primarily in delta F 508 homozygous) have not revealed significant improvement in CFRD or glucose tolerance. No studies are yet available regarding the effect of the highly effective triple therapy (elexacaftor/tezacaftor/ivacaftor) on CFRD or insulin secretion. CFTR modulators might affect development or progression of CFRD through many mechanisms including improving insulin secretion by correcting the CFTR defect directly, improving ductal function, reducing islet inflammation, and improving incretin secretion or by enhancing insulin sensitivity via reduced systemic inflammation and increased physical activity driven by improved lung function and quality of life. On the other hand, they can stimulate appetite and improve gastrointestinal function resulting in increased caloric intake and absorption, driving excessive weight gain and potentially increased insulin resistance. If the defect in insulin secretion is reversible then it is possible that initiation of CFTR modulators at a younger age might help prevent CFRD. Despite the advances in CF management, CFRD remains a challenge and knowledge continues to evolve. Future studies will drive better understanding of the role of highly effective CFTR modulators in CFRD.
机构:
Yale Univ, Dept Internal Med, Div Pulm Crit Care & Sleep Med, Sch Med, 300 Cedar St,TAC S419, New Haven, CT 06520 USAYale Univ, Dept Internal Med, Div Pulm Crit Care & Sleep Med, Sch Med, 300 Cedar St,TAC S419, New Haven, CT 06520 USA
Britto, Clemente J.
Taylor-Cousar, Jennifer L.
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机构:
Univ Colorado, Dept Med & Pediat, Div Pulm Sci & Crit Care Med, Anschutz Med Campus,1400 Jackson St,J318, Denver, CO 80206 USA
Univ Colorado, Div Pediat Pulmonol, Anschutz Med Campus,1400 Jackson St,J318, Denver, CO 80206 USAYale Univ, Dept Internal Med, Div Pulm Crit Care & Sleep Med, Sch Med, 300 Cedar St,TAC S419, New Haven, CT 06520 USA
机构:
Univ N Carolina, Cyst Fibrosis Res Ctr, Marsico Lung Inst, Chapel Hill, NC 27515 USA
Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC 27515 USAUniv N Carolina, Cyst Fibrosis Res Ctr, Marsico Lung Inst, Chapel Hill, NC 27515 USA
Gentzsch, Martina
Mall, Marcus A.
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机构:
Charite Univ Med Berlin, Dept Pediat Pulmonol Immunol & Intens Care Med, Augustenburger Pl 1, D-13353 Berlin, Germany
Berlin Inst Hlth, Berlin, Germany
Heidelberg Univ, German Ctr Lung Res, Translat Lung Res Ctr Heidelberg TLRC, Heidelberg, GermanyUniv N Carolina, Cyst Fibrosis Res Ctr, Marsico Lung Inst, Chapel Hill, NC 27515 USA
机构:
Prince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Univ Queensland, Ctr Clin Res, Fac Med, Brisbane, AustraliaPrince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Burke, Andrew
Thomson, Rachel M. M.
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机构:
Prince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Greenslopes Private Hosp, Gallipoli Med Res Fdn, Greenslopes, Qld, AustraliaPrince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Thomson, Rachel M. M.
Wainwright, Claire E. E.
论文数: 0引用数: 0
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机构:
Queensland Childrens Hosp, Dept Resp & Sleep Med, South Brisbane, Australia
Univ Queensland, Childrens Hlth Res Ctr, Fac Med, South Brisbane, AustraliaPrince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Wainwright, Claire E. E.
Bell, Scott C. C.
论文数: 0引用数: 0
h-index: 0
机构:
Prince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia
Univ Queensland, Childrens Hlth Res Ctr, Fac Med, South Brisbane, Australia
Translat Res Inst, Woolloongabba, AustraliaPrince Charles Hosp, Dept Thorac Med, Chermside, Qld, Australia