Genotype-stratified treatment for monogenic insulin resistance: a systematic review
Semple, R.K. ; Ahmad, A. LU
; Dudenhöffer-Pfeifer, M.
LU
; Fitipaldi, H.
LU
; Pomares-Millan, H.
LU
; Gomez, M.F.
LU
; Franks, P.W.
LU
and Brown, J. R.
(2023)
In Communications medicine
3(1).
- Abstract
- Background
Monogenic insulin resistance (IR) includes lipodystrophy and disorders of insulin signalling. We sought to assess the effects of interventions in monogenic IR, stratified by genetic aetiology.
Methods
Systematic review using PubMed, MEDLINE and Embase (1 January 1987 to 23 June 2021). Studies reporting individual-level effects of pharmacologic and/or surgical interventions in monogenic IR were eligible. Individual data were extracted and duplicates were removed. Outcomes were analysed for each gene and intervention, and in aggregate for partial, generalised and all lipodystrophy.
Results
10 non-randomised experimental studies, 8 case series, and 23 case reports meet inclusion criteria, all rated as... (More) - Background
Monogenic insulin resistance (IR) includes lipodystrophy and disorders of insulin signalling. We sought to assess the effects of interventions in monogenic IR, stratified by genetic aetiology.
Methods
Systematic review using PubMed, MEDLINE and Embase (1 January 1987 to 23 June 2021). Studies reporting individual-level effects of pharmacologic and/or surgical interventions in monogenic IR were eligible. Individual data were extracted and duplicates were removed. Outcomes were analysed for each gene and intervention, and in aggregate for partial, generalised and all lipodystrophy.
Results
10 non-randomised experimental studies, 8 case series, and 23 case reports meet inclusion criteria, all rated as having moderate or serious risk of bias. Metreleptin use is associated with the lowering of triglycerides and haemoglobin A1c (HbA1c) in all lipodystrophy (n = 111), partial (n = 71) and generalised lipodystrophy (n = 41), and in LMNA, PPARG, AGPAT2 or BSCL2 subgroups (n = 72,13,21 and 21 respectively). Body Mass Index (BMI) is lowered in partial and generalised lipodystrophy, and in LMNA or BSCL2, but not PPARG or AGPAT2 subgroups. Thiazolidinediones are associated with improved HbA1c and triglycerides in all lipodystrophy (n = 13), improved HbA1c in PPARG (n = 5), and improved triglycerides in LMNA (n = 7). In INSR-related IR, rhIGF-1, alone or with IGFBP3, is associated with improved HbA1c (n = 17). The small size or absence of other genotype-treatment combinations preclude firm conclusions.
Conclusions
The evidence guiding genotype-specific treatment of monogenic IR is of low to very low quality. Metreleptin and Thiazolidinediones appear to improve metabolic markers in lipodystrophy, and rhIGF-1 appears to lower HbA1c in INSR-related IR. For other interventions, there is insufficient evidence to assess efficacy and risks in aggregated lipodystrophy or genetic subgroups. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/628dea2f-8c0b-4129-a3cf-2d66b2b14a11
- author
- Semple, R.K.
; Ahmad, A.
LU
; Dudenhöffer-Pfeifer, M.
LU
; Fitipaldi, H.
LU
; Pomares-Millan, H.
LU
; Gomez, M.F.
LU
; Franks, P.W.
LU
and Brown, J. R.
- author collaboration
- organization
- publishing date
- 2023
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Communications medicine
- volume
- 3
- issue
- 1
- article number
- 134
- publisher
- Nature Publishing Group
- external identifiers
-
- scopus:85174334890
- ISSN
- 2730-664X
- DOI
- 10.1038/s43856-023-00368-9
- language
- English
- LU publication?
- yes
- id
- 628dea2f-8c0b-4129-a3cf-2d66b2b14a11
- date added to LUP
- 2025-09-30 07:43:04
- date last changed
- 2025-09-30 07:43:20
@article{628dea2f-8c0b-4129-a3cf-2d66b2b14a11,
abstract = {{Background<br/>Monogenic insulin resistance (IR) includes lipodystrophy and disorders of insulin signalling. We sought to assess the effects of interventions in monogenic IR, stratified by genetic aetiology.<br/><br/>Methods<br/>Systematic review using PubMed, MEDLINE and Embase (1 January 1987 to 23 June 2021). Studies reporting individual-level effects of pharmacologic and/or surgical interventions in monogenic IR were eligible. Individual data were extracted and duplicates were removed. Outcomes were analysed for each gene and intervention, and in aggregate for partial, generalised and all lipodystrophy.<br/><br/>Results<br/>10 non-randomised experimental studies, 8 case series, and 23 case reports meet inclusion criteria, all rated as having moderate or serious risk of bias. Metreleptin use is associated with the lowering of triglycerides and haemoglobin A1c (HbA1c) in all lipodystrophy (n = 111), partial (n = 71) and generalised lipodystrophy (n = 41), and in LMNA, PPARG, AGPAT2 or BSCL2 subgroups (n = 72,13,21 and 21 respectively). Body Mass Index (BMI) is lowered in partial and generalised lipodystrophy, and in LMNA or BSCL2, but not PPARG or AGPAT2 subgroups. Thiazolidinediones are associated with improved HbA1c and triglycerides in all lipodystrophy (n = 13), improved HbA1c in PPARG (n = 5), and improved triglycerides in LMNA (n = 7). In INSR-related IR, rhIGF-1, alone or with IGFBP3, is associated with improved HbA1c (n = 17). The small size or absence of other genotype-treatment combinations preclude firm conclusions.<br/><br/>Conclusions<br/>The evidence guiding genotype-specific treatment of monogenic IR is of low to very low quality. Metreleptin and Thiazolidinediones appear to improve metabolic markers in lipodystrophy, and rhIGF-1 appears to lower HbA1c in INSR-related IR. For other interventions, there is insufficient evidence to assess efficacy and risks in aggregated lipodystrophy or genetic subgroups.}},
author = {{Semple, R.K. and Ahmad, A. and Dudenhöffer-Pfeifer, M. and Fitipaldi, H. and Pomares-Millan, H. and Gomez, M.F. and Franks, P.W. and Brown, J. R.}},
issn = {{2730-664X}},
language = {{eng}},
number = {{1}},
publisher = {{Nature Publishing Group}},
series = {{Communications medicine}},
title = {{Genotype-stratified treatment for monogenic insulin resistance: a systematic review}},
url = {{http://dx.doi.org/10.1038/s43856-023-00368-9}},
doi = {{10.1038/s43856-023-00368-9}},
volume = {{3}},
year = {{2023}},
}