Dipeptidyl Peptidase-IV Inhibitors Are Efficient Adjunct Therapy in HNF1A Maturity-Onset Diabetes of the Young Patients-Report of Two Cases

被引:28
作者
Katra, Barbara [1 ,2 ]
Klupa, Tomasz [1 ,2 ]
Skupien, Jan [1 ,2 ,3 ]
Szopa, Magdalena [1 ,2 ]
Nowak, Natalia [1 ]
Borowiec, Maciej [4 ]
Kozek, Elzbieta [1 ,2 ]
Malecki, Maciej T. [1 ,2 ]
机构
[1] Jagiellonian Univ, Coll Med, Dept Metab Dis, PL-31501 Krakow, Poland
[2] Univ Hosp, Krakow, Poland
[3] Joslin Diabet Ctr, Sect Genet & Epidemiol, Boston, MA 02215 USA
[4] Med Univ Lodz, Dept Pediat, Lodz, Poland
关键词
INSULIN; SULFONYLUREAS; MUTATIONS;
D O I
10.1089/dia.2009.0159
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In HNF1A maturity-onset diabetes of the young (MODY), sulfonylurea (SU) is the first-line treatment. Over time, such therapy fails, and additional treatment is required. Dipeptidyl peptidase IV (DPP-IV) inhibitors are new agents that lower blood glucose by prolonging the activity of circulating incretins. Methods: We applied DPP-IV inhibitors in two HNF1A MODY patients whose earlier therapeutic regimen included SU. Results: Case 1, a 39-year-old woman, a carrier of the ArgR171X HNF1A mutation, with a 7-year history of diabetes was on 160mg of gliclazide and 2,000mg of metformin. Her initial hemoglobin A1c (HbA1c) level was 7.2%, while the mean glucose level on the CGMS (R) (Medtronic, Northridge, CA) record was 162mg/dL. Sitagliptine, in a dose of 100mg/day, was added to the previous treatment. Case 2, a 62-year-old woman, a carrier of the IVS7nt-6G>A mutation, with a 41-year history of diabetes was treated with 240mg/day gliclazide and 6 IU of insulin/day. Her initial HbA1c was 8.8%, and average glycemia reached 172mg/dL. In her case, we started the combined therapy with 50mg of vildagliptine twice daily. Patients were reexamined after 3 months, and HbA1c fell to 6.3% in both subjects. Similarly, significant improvement in glycemic control on CGMS was observed as the average glycemia decreased to 114mg/dL and 134mg/dL in Case 1 and Case 2, respectively. No episodes of hypoglycemia or other side effects were recorded. As intravenous glucose tolerance tests (IVGTTs) were performed before and after DPP-IV implementation, we were able to assess their impact on insulin secretion under fasting conditions. We saw a substantial rise in insulin level increment during IVGTT (by 9.8 and 13.4 mIU/L in Case 1 and Case 2, respectively). Conclusions: DPP-IV inhibitors may be an effective tool of combined therapy in HNF1A MODY, and they seem to improve beta-cell function under fasting conditions.
引用
收藏
页码:313 / 316
页数:4
相关论文
共 12 条
[1]   Efficacy and safety of incretin therapy in type 2 diabetes - Systematic review and meta-analysis [J].
Amori, Renee E. ;
Lau, Joseph ;
Pittas, Anastassios G. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 298 (02) :194-206
[2]   Treatment with the Dipeptidyl Peptidase-4 Inhibitor Vildagliptin Improves Fasting Islet-Cell Function in Subjects with Type 2 Diabetes [J].
D'Alessio, David A. ;
Denney, Amanda M. ;
Hermiller, Linda M. ;
Prigeon, Ronald L. ;
Martin, Julie M. ;
Tharp, William G. ;
Saylan, Monica Liqueros ;
He, YanLing ;
Dunning, Beth E. ;
Foley, James E. ;
Pratley, Richard E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (01) :81-88
[3]   The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes [J].
Drucker, Daniel J. ;
Nauck, Michael A. .
LANCET, 2006, 368 (9548) :1696-1705
[4]   Treatment of HNF1-alpha MODY with the DPP-4 inhibitor Sitagliptin [J].
Lumb, Alistair N. ;
Gallen, Ian W. .
DIABETIC MEDICINE, 2009, 26 (02) :189-190
[5]   Can geneticists help clinicians to understand and treat non-autoimmune diabetes? [J].
Malecki, Maciej T. ;
Mlynarski, Wojciech ;
Skupien, Jan .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2008, 82 :S83-S93
[6]   Renal malformations may be linked to mutations in the hepatocyte nuclear factor-1α (MODY3) gene [J].
Malecki, MT ;
Skupien, J ;
Gorczynska-Kosiorz, S ;
Klupa, T ;
Nazim, J ;
Moczulski, DK ;
Sieradzki, J .
DIABETES CARE, 2005, 28 (11) :2774-2776
[7]   Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1α gene mutations:: evidence for pharmacogenetics in diabetes [J].
Pearson, ER ;
Liddell, WG ;
Shepherd, M ;
Corrall, RJ ;
Hattersley, AT .
DIABETIC MEDICINE, 2000, 17 (07) :543-545
[8]   Genetic cause of hyperglycaemia and response to treatment in diabetes [J].
Pearson, ER ;
Starkey, BJ ;
Powell, RJ ;
Gribble, FM ;
Clark, PM ;
Hattersley, AT .
LANCET, 2003, 362 (9392) :1275-1281
[9]   Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations [J].
Pearson, Ewan R. ;
Flechtner, Isabelle ;
Njolstad, Pal R. ;
Malecki, Maciej T. ;
Flanagan, Sarah E. ;
Larkin, Brian ;
Ashcroft, Frances M. ;
Klimes, Iwar ;
Codner, Ethel ;
Iotova, Violeta ;
Slingerland, Annabelle S. ;
Shield, Julian ;
Robert, Jean-Jacques ;
Holst, Jens J. ;
Clark, Penny M. ;
Ellard, Sian ;
Sovik, Oddmund ;
Polak, Michel ;
Hattersley, Andrew T. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (05) :467-477
[10]   No deterioration in glycemic control in HNF-1 α maturity-onset diabetes of the young following transfer from long term insulin to sulphonylureas [J].
Shepherd, M ;
Pearson, ER ;
Houghton, J ;
Salt, G ;
Ellard, S ;
Hattersley, AT .
DIABETES CARE, 2003, 26 (11) :3191-3192