Zusammenfassung
Diabetiker leiden langfristig an zahlreichen Folgeerkrankungen, darunter auch sensible
Polyneuropathien. Im Rahmen der diabetischen Polyneuropathie (DPNP) treten häufig
Schmerzen unterschiedlichster Art, Ausprägung und Dauer auf. Zur Therapie dieser Beschwerden
gibt es zahlreiche pharmakotherapeutische Angriffspunkte, auch Antidepressiva sind
von Bedeutung. Ein neuer Wirkstoff, der selektive Serotonin- und Noradrenalin-Wiederaufnahmehemmer
Duloxetin, scheint in der Schmerzbehandlung ähnlich wirksam zu sein wie etablierte
Substanzen. Duloxetin (60 mg einmal oder 60 mg zweimal täglich) reduzierte im Vergleich
zu Plazebo ab der ersten Behandlungswoche signifikant die Schmerzen bei DPNP. Die
am häufigsten beobachteten Nebenwirkungen waren Übelkeit, Schläfrigkeit, Schwindel,
Obstipation und Müdigkeit. Es zeigte sich im Mittel keine klinisch relevante Erhöhung
von Blutdruck und Puls sowie keine Gewichtszunahme. Duloxetin bietet damit eine neue
Therapieoption bei DPNP. Im Therapiealgorithmus sollen die einzelnen Substanzen individuell,
auch unter Berücksichtigiung ihres Nebenwirkungsprofils, eingesetzt werden. Zur Unterstützung
der Schmerzbewältigung dienen supportive psychologische Therapieverfahren.
Summary
Diabetics develop numerous chronic associated diseases, among them sensory polyneuropathy.
Diabetic polyneuropathy (DPN) often causes pain of various kinds, degree and duration.
There are many pharmacological approaches: antidepressants are also important. Duloxetine
is a recently approved dual action serotonin and noradrenaline re-uptake inhibitor
that in its analgesic efficacy is comparable to established drugs. Duloxetine, in
a dosage of 60 mg x 1 or x 2 daily, significantly reduces, from the first week of
administration, the pain of DPN, when compared with a placebo. The most commonly observed
side effects have been nausea, sleepiness, constipation and fatigue. On average duloxetine
has not shown any clinically relevant increase in blood pressure, pulse rate and
weight. It thus offers a new option as part of the treatment of pain caused by DPN.
The various drugs should be considered individually in any treatment algorithm, also
taking into account their side effects. Psychotherapeutic methods serve to support
the overcoming of pain.
Literatur
- 1
Backonja M, Beydoun A, Edwards K R.
Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes
mellitus: a randomized controlled trial.
JAMA.
1998;
280
1831-1836
- 2
Boulton A J, Vinik A I, Arezzo J C. et al., American Diabetes Association .
Diabetic neuropathies: a statement by the American Diabetes Association.
Diabetes Care.
2005;
28
956-962
- 3
Daousi C, MacFarlane I A, Woodward A. et al .
Chronic painful peripheral neuropathy in an urban community: a controlled comparison
of people with and without diabetes.
Diabetic Med.
2004;
21
976-982
- 4
The Diabetes Control and Complications Trial Research Group .
The effect of intensive treatment of diabetes on the development and progression of
long-term complications in insulin-dependent diabetes mellitus.
N Engl J Med.
1993;
329
977-986
- 5 Fachinformation CYMBALTA.
- 6
Finnerup N B, Otto M, McQuay H J, Jensen T S, Sindrup S H.
Algorithm for neuropathic pain treatment: an evidence based proposal.
Pain.
2005;
118
289-305
- 7
Gaede P, Vedel P, Larsen N, Jensen G V, Parving H H, Pedersen O.
Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes.
N Engl J Med.
2003;
348
383-393
- 8
Galer B S, Gianas A, Jensen M P.
Painful diabetic polyneuropathy: epidemiology, pain description, and quality of life.
Diabetes Res Clin Pract,.
2000;
47
123-128
- 9
Goldstein D J, Lu Y, Detke M J, Lee T C, Iyengar S.
Duloxetine vs. placebo in patients with painful diabetic neuropathy.
Pain.
2005;
116
109-118
- 10
Griesing T, Freeman R, Rosenstock J, Sharma U, LaMoreaux L, Emir B, Siffert J.
Efficacy, safety and tolerability of pregabalin treatment for diabetic peripheral
neuropathy: findings from 6 randomized controlled trials.
Diabetologia.
2005;
48
, (Suppl 1)
A351
- 11
Herman W H, Kennedy L.
Underdiagnosis of peripheral neuropathy in type 2 diabetes.
Diabetes Care.
2005;
28
1480-1481
- 12
Iyengar S, Webster A A, Hemrick-Luecke S K, Xu J Y, Simmons R M.
Efficacy of duloxetine, a potent and balanced serotonin-norepinephrine reuptake inhibitor
in persistent pain models in rats.
J Pharmacol Exp Ther.
2004;
311
576-584
- 13
Lantz R J, Gillespie T A, Rash T J. et al .
Metabolism, excretion, and pharmacokinetics of duloxetine in healthy human subjects.
Drug Metab Dispos.
2003;
21
1142-1150
- 14
Magni G, Moreschi C, Rigatti-Luchini S, Merskey H.
Prospective study on the relationship between depressive symptoms and chronic musculoskeletal
pain.
Pain.
1994;
56
289-497
- 15
Max M B, Lynch S A, Smoller B, Dubner R.
Effects of desipramine, amitriptyline, and fluoxetine on pain in diabetic neuropathy.
N Engl J Med.
1992;
326
1287-1288
- 16
Mendell J R, Sahenk Z.
Clinical practice. Painful sensory neuropathy.
N Engl J Med.
2003;
348
1243-1255
- 17
Polydefkis M, Griffin J W, McArthur J.
New insights into diabetic polyneuropathy.
JAMA.
2003;
290
1371-1376
- 18
Raskin J, Pritchett Y L, Wang F, D’Souza D N, Waninger A L, Iyengar S, Wernicke J F.
A double-blind, randomized multicenter trial comparing duloxetine with placebo in
the management of diabetic peripheral neuropathic pain.
Pain Med.
2005;
6
346-356
- 19 Wenicke J F, Lu Y L, D’Souza D N, Waninger A, Tran P, Iyengar S, Raskin J. A randomized
controlled trial of duloxetine in diabetic peripheral neuropathic pain. Neurology
2006; im Druck
- 20
Tesfaye S, Chaturvedi N, Eaton S E. et al. EURODIAB Prospective Complications Study
Group .
Vascular risk factors and diabetic neuropathy.
N Engl J Med.
2005;
352
341-350
- 21 Wernicke J F. et al .Presented at the 56th Annual Meeting of the AAN;. San Francisco,
CA; April 24 - May 1 2004
- 22 www.deutsche-diabetes-gesellschaft.de/Praxis-Leitlinien/Diabetische Neuropathie/Aktualisierte
Version Feb 2005 2005
- 23
Ziegler D, Rathmann W, Haastert B, Füchsle-Reiter A, Löwel H, Mielck A.
Prevalence of polyneuropathy in impaired glucose tolerance and diabetes. The MONICA/KORA
Augsburg Surveys and Myocardial Infarction Registry (KORA-A-Study).
Diabetologia.
2005;
48 (Suppl 1)
A364-A365
- 24
Ziegler D, Nowak H, Kempler P, Vargha P, Low P A.
Treatment of symptomatic diabetic polyneuropathy with the antioxidant a-lipoic acid:
a meta-analysis.
Diabetic Med.
2004;
21
114-121
Prof. Dr. Dan Ziegler
Deutsches Diabetes-Zentrum, Heinrich-Heine-Universität Düsseldorf
Auf’m Hennekamp 65
40225 Düsseldorf
Email: dan.ziegler@ddz.uni-duesseldorf.de