TY - JOUR
T1 - Metformin use and risk of myeloproliferative neoplasms - a Danish population-based case-control study
AU - Kristensen, Daniel Tuyet
AU - Øvlisen, Andreas Kiesbye
AU - Jakobsen, Lasse Hjort
AU - Severinsen, Marianne Tang
AU - Hannig, Louise Hur
AU - Starklint, Jørn
AU - Hilsøe, Morten Hagemann
AU - Vallentin, Anders Pommer
AU - Brabrand, Mette
AU - Hasselbalch, Hans Carl
AU - El Galaly, Tarec Christoffer
AU - Roug, Anne Stidsholt
N1 - Copyright © 2024 American Society of Hematology.
PY - 2024/8/27
Y1 - 2024/8/27
N2 - Previous studies have suggested that metformin has beneficial effects beyond its glucose-lowering properties, particularly in terms of its potential as an antineoplastic and cancer-preventive agent. In this study, we aimed to investigate the association between metformin use and the risk of myeloproliferative neoplasms (MPN). We conducted a population-based case-control study using Danish registers. Cases with MPN diagnosed between 2010 and 2018 were identified, and metformin use before the MPN diagnosis was ascertained. We compared metformin use among cases with MPN and an age- and sex-matched control group from the Danish general population to estimate age- and sex-adjusted odds ratios (ORs) and fully adjusted ORs (aORs) for the association between metformin use and risk of MPN. The study population included 3816 cases and 19 080 controls. Overall, 7.0% of cases and 8.2% of controls were categorized as ever-users of metformin, resulting in an OR for MPN of 0.84 (95% confidence interval [CI], 0.73-0.96) and an aOR of 0.70 (95% CI, 0.61-0.81). Long-term metformin use (≥5 years) was more infrequent and comprised 1.1% of cases and 2.0% of controls, resulting in an OR of 0.57 (95% CI, 0.42-0.79) and an aOR of 0.45 (95% CI, 0.33-0.63). A dose-response relationship was observed when cumulative duration of treatment was analyzed, and this was consistent in stratified analyses of sex, age, and MPN subtypes. In conclusion, metformin use was associated with significantly lower odds of an MPN diagnosis, indicating its potential cancer-preventive effect. Given the retrospective design, causality cannot be inferred.
AB - Previous studies have suggested that metformin has beneficial effects beyond its glucose-lowering properties, particularly in terms of its potential as an antineoplastic and cancer-preventive agent. In this study, we aimed to investigate the association between metformin use and the risk of myeloproliferative neoplasms (MPN). We conducted a population-based case-control study using Danish registers. Cases with MPN diagnosed between 2010 and 2018 were identified, and metformin use before the MPN diagnosis was ascertained. We compared metformin use among cases with MPN and an age- and sex-matched control group from the Danish general population to estimate age- and sex-adjusted odds ratios (ORs) and fully adjusted ORs (aORs) for the association between metformin use and risk of MPN. The study population included 3816 cases and 19 080 controls. Overall, 7.0% of cases and 8.2% of controls were categorized as ever-users of metformin, resulting in an OR for MPN of 0.84 (95% confidence interval [CI], 0.73-0.96) and an aOR of 0.70 (95% CI, 0.61-0.81). Long-term metformin use (≥5 years) was more infrequent and comprised 1.1% of cases and 2.0% of controls, resulting in an OR of 0.57 (95% CI, 0.42-0.79) and an aOR of 0.45 (95% CI, 0.33-0.63). A dose-response relationship was observed when cumulative duration of treatment was analyzed, and this was consistent in stratified analyses of sex, age, and MPN subtypes. In conclusion, metformin use was associated with significantly lower odds of an MPN diagnosis, indicating its potential cancer-preventive effect. Given the retrospective design, causality cannot be inferred.
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Case-Control Studies
KW - Denmark/epidemiology
KW - Female
KW - Humans
KW - Hypoglycemic Agents/therapeutic use
KW - Male
KW - Metformin/therapeutic use
KW - Middle Aged
KW - Myeloproliferative Disorders/epidemiology
KW - Odds Ratio
KW - Risk Factors
U2 - 10.1182/bloodadvances.2023012266
DO - 10.1182/bloodadvances.2023012266
M3 - Journal article
C2 - 38758071
SN - 2473-9529
VL - 8
SP - 4478
EP - 4485
JO - Blood Advances
JF - Blood Advances
IS - 16
ER -