Skip to main content
Erschienen in: CNS Drugs 11/2006

01.11.2006 | Adis Spotlight

Spotlight on Eletriptan in Migraine

verfasst von: Paul L. McCormack, Gillian M. Keating

Erschienen in: CNS Drugs | Ausgabe 11/2006

Einloggen, um Zugang zu erhalten

Abstract

Eletriptan (Relpax®)2 is an orally administered, lipophilic, highly selective serotonin 5-HT1B/1D receptor agonist (‘triptan’) that is effective in the acute treatment of moderate to severe migraine attacks in adults. It has a rapid onset of action and demonstrates superiority over placebo as early as 30 minutes after the administration of a single 40 or 80mg oral dose. The efficacy of eletriptan 20mg was similar to that of sumatriptan 100mg, while eletriptan 40 and 80mg displayed greater efficacy than sumatriptan 50 or 100mg for most endpoints. Eletriptan 40mg was generally superior to naratriptan 2.5mg and equivalent to almotriptan 12.5mg, rizatriptan 10mg and zolmitriptan 2.5mg, while eletriptan 80mg was superior to zolmitriptan 2.5mg for most efficacy parameters. Eletriptan 40 and 80mg were consistently superior to ergotamine/caffeine. Eletriptan is generally well tolerated, reduces time lost from normal activities, improves patients’ health-related quality of life and appears to be at least as, if not more, cost effective than sumatriptan. Eletriptan is therefore a useful addition to the triptan family and a first-line treatment option in the acute management of migraine attacks.
Literatur
1.
Zurück zum Zitat Napier C, Stewart M, Melrose H, et al. Characterisation of the 5-HT receptor binding profile of eletriptan and kinetics of [3H]eletriptan binding at human 5-HT1B and 5-HT1D receptors. Eur J Pharmacol 1999; 368: 259–68PubMedCrossRef Napier C, Stewart M, Melrose H, et al. Characterisation of the 5-HT receptor binding profile of eletriptan and kinetics of [3H]eletriptan binding at human 5-HT1B and 5-HT1D receptors. Eur J Pharmacol 1999; 368: 259–68PubMedCrossRef
2.
Zurück zum Zitat Bardsley-Elliot A, Noble S. Eletriptan. CNS Drugs 1999 Oct; 12(4): 325–33CrossRef Bardsley-Elliot A, Noble S. Eletriptan. CNS Drugs 1999 Oct; 12(4): 325–33CrossRef
3.
Zurück zum Zitat Willems E, De Vries P, Heiligers JPC, et al. Porcine carotid vascular effects of eletriptan (UK-116,044): a new 5-HT1B/1D receptor agonist with anti-migraine activity. Naunyn Schmiedebergs Arch Pharmacol 1998; 358: 212–9PubMedCrossRef Willems E, De Vries P, Heiligers JPC, et al. Porcine carotid vascular effects of eletriptan (UK-116,044): a new 5-HT1B/1D receptor agonist with anti-migraine activity. Naunyn Schmiedebergs Arch Pharmacol 1998; 358: 212–9PubMedCrossRef
4.
Zurück zum Zitat Gupta P, Butler P, Shepperson NB, et al. The in vivo pharmacological profile of eletriptan (UK-116,044): a potent and novel 5-HT1B/1D receptor agonist. Eur J Pharmacol 2000 Jun 9; 398(1): 73–81PubMedCrossRef Gupta P, Butler P, Shepperson NB, et al. The in vivo pharmacological profile of eletriptan (UK-116,044): a potent and novel 5-HT1B/1D receptor agonist. Eur J Pharmacol 2000 Jun 9; 398(1): 73–81PubMedCrossRef
5.
Zurück zum Zitat MaassenVanDenBrink A, van den Broek RW, de Vries R, et al. Craniovascular selectivity of eletriptan and sumatriptan in human isolated blood vessels. Neurology 2000 Nov 28; 55(10): 1524–30PubMedCrossRef MaassenVanDenBrink A, van den Broek RW, de Vries R, et al. Craniovascular selectivity of eletriptan and sumatriptan in human isolated blood vessels. Neurology 2000 Nov 28; 55(10): 1524–30PubMedCrossRef
6.
Zurück zum Zitat Gupta P, Brown D, Butler P, et al. Preclinical in vivo pharmacology of eletriptan (UK-116,044): a potent and selective partial agonist at the “5HT1D-like” receptor [abstract no. 77]. Cephalalgia 1996; 16: 386 Gupta P, Brown D, Butler P, et al. Preclinical in vivo pharmacology of eletriptan (UK-116,044): a potent and selective partial agonist at the “5HT1D-like” receptor [abstract no. 77]. Cephalalgia 1996; 16: 386
7.
Zurück zum Zitat Knyihar-Csillik E, Tajti J, Csillik AE, et al. Effects of eletriptan on the peptidergic innervation of the cerebral dura mater and trigeminal ganglion, and on the expression of c-fos and c-jun in the trigeminal complex of the rat in an experimental migraine model. Eur J Neurosci 2000 Nov; 12(11): 3991–4002PubMedCrossRef Knyihar-Csillik E, Tajti J, Csillik AE, et al. Effects of eletriptan on the peptidergic innervation of the cerebral dura mater and trigeminal ganglion, and on the expression of c-fos and c-jun in the trigeminal complex of the rat in an experimental migraine model. Eur J Neurosci 2000 Nov; 12(11): 3991–4002PubMedCrossRef
8.
Zurück zum Zitat Goadsby PJ, Hoskin KL. Differential effects of low dose CP122,288 and eletriptan on Fos expression due to stimulation of the superior sagittal sinus in cat. Pain 1999; 82: 15–22PubMedCrossRef Goadsby PJ, Hoskin KL. Differential effects of low dose CP122,288 and eletriptan on Fos expression due to stimulation of the superior sagittal sinus in cat. Pain 1999; 82: 15–22PubMedCrossRef
9.
Zurück zum Zitat Lambert GA, Boers PM, Hoskin KL, et al. Suppression by eletriptan of the activation of trigeminovascular sensory neurons by glyceryl trinitrate. Brain Res 2002 Oct 25; 953(1–2): 181–8PubMedCrossRef Lambert GA, Boers PM, Hoskin KL, et al. Suppression by eletriptan of the activation of trigeminovascular sensory neurons by glyceryl trinitrate. Brain Res 2002 Oct 25; 953(1–2): 181–8PubMedCrossRef
10.
Zurück zum Zitat Johnson DE, Rollema H, Schmidt AW, et al. Serotonergic effects and extracellular brain levels of eletriptan, zolmitriptan and sumatriptan in rat brain. Eur J Pharmacol 2001 Aug 17; 425(3): 203–10PubMedCrossRef Johnson DE, Rollema H, Schmidt AW, et al. Serotonergic effects and extracellular brain levels of eletriptan, zolmitriptan and sumatriptan in rat brain. Eur J Pharmacol 2001 Aug 17; 425(3): 203–10PubMedCrossRef
11.
Zurück zum Zitat Evans DC, O’Connor D, Scott-Stevens P, et al. Central sites of action affect the antimigraine efficacy of 5-HT1B/1D receptor agonists [abstract]. Headache Q 2001; 12(1): 45 Evans DC, O’Connor D, Scott-Stevens P, et al. Central sites of action affect the antimigraine efficacy of 5-HT1B/1D receptor agonists [abstract]. Headache Q 2001; 12(1): 45
12.
Zurück zum Zitat Evans DC, O’Connor D, Lake BG, et al. Eletriptan metabolism by human hepatic CYP450 enzymes and transport by human P-glycoprotein. Drug Metab Dispos 2003 Jul; 31(7): 861–9PubMedCrossRef Evans DC, O’Connor D, Lake BG, et al. Eletriptan metabolism by human hepatic CYP450 enzymes and transport by human P-glycoprotein. Drug Metab Dispos 2003 Jul; 31(7): 861–9PubMedCrossRef
13.
Zurück zum Zitat Milton KA, Scott NR, Allen MJ, et al. Pharmacokinetics, pharmacodynamics, and safety of the 5-HT1B/1D agonist eletriptan following intravenous and oral administration. J Clin Pharmacol 2002 May; 42(5): 528–39PubMedCrossRef Milton KA, Scott NR, Allen MJ, et al. Pharmacokinetics, pharmacodynamics, and safety of the 5-HT1B/1D agonist eletriptan following intravenous and oral administration. J Clin Pharmacol 2002 May; 42(5): 528–39PubMedCrossRef
14.
15.
Zurück zum Zitat Shah AK, Harris SC, Greenhalgh C, et al. The pharmacokinetics and safety of single escalating oral doses of eletriptan. J Clin Pharmacol 2002 May; 42(5): 520–7PubMedCrossRef Shah AK, Harris SC, Greenhalgh C, et al. The pharmacokinetics and safety of single escalating oral doses of eletriptan. J Clin Pharmacol 2002 May; 42(5): 520–7PubMedCrossRef
16.
17.
Zurück zum Zitat Johnson BF, Shah A, Law G. The absorption kinetics of eletriptan in migraineurs [abstract]. Headache 1997 May; 37(5): 315 Johnson BF, Shah A, Law G. The absorption kinetics of eletriptan in migraineurs [abstract]. Headache 1997 May; 37(5): 315
18.
Zurück zum Zitat Milton KA, Allen MJ, Abel S, et al. The safety, tolerability, and pharmacokinetics of oral and intravenous eletriptan, a potent and selective ‘5-HT1D-like’ receptor partial agonist [abstract]. Headache 1997 May; 37(5): 324 Milton KA, Allen MJ, Abel S, et al. The safety, tolerability, and pharmacokinetics of oral and intravenous eletriptan, a potent and selective ‘5-HT1D-like’ receptor partial agonist [abstract]. Headache 1997 May; 37(5): 324
19.
Zurück zum Zitat Morgan P, Rance DJ, James G, et al. An in vitro-in vivo correlation of eletriptan pharmacokinetics and metabolism in rat, dog, and human [abstract]. Headache 1997 May; 37(5): 324 Morgan P, Rance DJ, James G, et al. An in vitro-in vivo correlation of eletriptan pharmacokinetics and metabolism in rat, dog, and human [abstract]. Headache 1997 May; 37(5): 324
20.
Zurück zum Zitat Milton KA, Allen MJ, Abel S. The safety, tolerability and pharmacokinetics of intravenous eletriptan (UK-116,044), a new potent and-selective ‘5HT1D-like’ receptor agonist [abstract no. 76]. Cephalalgia 1996 Aug; 16(5): 385 Milton KA, Allen MJ, Abel S. The safety, tolerability and pharmacokinetics of intravenous eletriptan (UK-116,044), a new potent and-selective ‘5HT1D-like’ receptor agonist [abstract no. 76]. Cephalalgia 1996 Aug; 16(5): 385
21.
Zurück zum Zitat Hyland R, Jones BC, McCleverty P, et al. In vitro metabolism of eletriptan in human liver microsomes [abstract no. P.34]. Cephalalgia 1998; 18: 404 Hyland R, Jones BC, McCleverty P, et al. In vitro metabolism of eletriptan in human liver microsomes [abstract no. P.34]. Cephalalgia 1998; 18: 404
22.
Zurück zum Zitat Färkkilä M, Olesen J, Dahlöf C, et al. Eletriptan for the treatment of migraine in patients with previous poor response or tolerance to oral sumatriptan. Cephalalgia 2003; 23: 463–71PubMedCrossRef Färkkilä M, Olesen J, Dahlöf C, et al. Eletriptan for the treatment of migraine in patients with previous poor response or tolerance to oral sumatriptan. Cephalalgia 2003; 23: 463–71PubMedCrossRef
23.
Zurück zum Zitat Fukuuchi Y, Eletriptan Steering Committee in Japan. Efficacy and safety of eletriptan 20 mg, 40 mg and 80 mg in Japanese migraineurs. Cephalalgia 2002 Jul; 22(6): 416–23CrossRef Fukuuchi Y, Eletriptan Steering Committee in Japan. Efficacy and safety of eletriptan 20 mg, 40 mg and 80 mg in Japanese migraineurs. Cephalalgia 2002 Jul; 22(6): 416–23CrossRef
24.
Zurück zum Zitat Stark R, Dahlof C, Haughie S, et al. Efficacy, safety and tolerability of oral eletriptan in the acute treatment of migraine: results of a phase III, multicentre, placebo-controlled study across three attacks. Cephalalgia 2002 Feb; 22(1): 23–32PubMedCrossRef Stark R, Dahlof C, Haughie S, et al. Efficacy, safety and tolerability of oral eletriptan in the acute treatment of migraine: results of a phase III, multicentre, placebo-controlled study across three attacks. Cephalalgia 2002 Feb; 22(1): 23–32PubMedCrossRef
25.
Zurück zum Zitat Sheftell F, Ryan R, Pitman V. Efficacy, safety, and tolerability of oral eletriptan for treatment of acute migraine: a multicenter, double-blind, placebo-controlled study conducted in the United States. Headache 2003 Mar; 43(3): 202–13PubMedCrossRef Sheftell F, Ryan R, Pitman V. Efficacy, safety, and tolerability of oral eletriptan for treatment of acute migraine: a multicenter, double-blind, placebo-controlled study conducted in the United States. Headache 2003 Mar; 43(3): 202–13PubMedCrossRef
26.
Zurück zum Zitat Färkkilä M, Eletriptan Steering Committee. A dose-finding study of eletriptan (UK-116,044) (5–30 mg) for the acute treatment of migraine [abstract no. 81]. Cephalalgia 1996; 16: 387–8 Färkkilä M, Eletriptan Steering Committee. A dose-finding study of eletriptan (UK-116,044) (5–30 mg) for the acute treatment of migraine [abstract no. 81]. Cephalalgia 1996; 16: 387–8
27.
Zurück zum Zitat Goadsby PJ, Ferrari MD, Olesen J, et al. Eletriptan in acute migraine: a double-blind, placebo-controlled comparison to sumatriptan. Eletriptan Steering Committee. Neurology 2000 Jan 11; 54(1): 156–63 Goadsby PJ, Ferrari MD, Olesen J, et al. Eletriptan in acute migraine: a double-blind, placebo-controlled comparison to sumatriptan. Eletriptan Steering Committee. Neurology 2000 Jan 11; 54(1): 156–63
28.
Zurück zum Zitat Mathew NT, Schoenen J, Winner P, et al. Comparative efficacy of eletriptan 40 mg versus sumatriptan 100 mg. Headache 2003 Mar; 43(3): 214–22PubMedCrossRef Mathew NT, Schoenen J, Winner P, et al. Comparative efficacy of eletriptan 40 mg versus sumatriptan 100 mg. Headache 2003 Mar; 43(3): 214–22PubMedCrossRef
29.
Zurück zum Zitat Sandrini G, Färkkilä M, Burgess G, et al. Eletriptan vs sumatriptan: a double-blind, placebo-controlled, multiple migraine attack study. Neurology 2002 Oct 22; 59(8): 1210–7PubMedCrossRef Sandrini G, Färkkilä M, Burgess G, et al. Eletriptan vs sumatriptan: a double-blind, placebo-controlled, multiple migraine attack study. Neurology 2002 Oct 22; 59(8): 1210–7PubMedCrossRef
30.
Zurück zum Zitat Diener HC, Ryan R, Sun W, et al. The 40-mg dose of eletriptan: comparative efficacy and tolerability versus sumatriptan 100 mg. Eur J Neurol 2004 Feb; 11(2): 125–34PubMedCrossRef Diener HC, Ryan R, Sun W, et al. The 40-mg dose of eletriptan: comparative efficacy and tolerability versus sumatriptan 100 mg. Eur J Neurol 2004 Feb; 11(2): 125–34PubMedCrossRef
31.
Zurück zum Zitat Lainez M, Evers S, Kinge E, et al. Preference for rizatriptan 10-mg wafer vs. eletriptan 40-mg tablet for acute treatment of migraine. Cephalalgia 2006 Mar; 26(3): 246–56 Lainez M, Evers S, Kinge E, et al. Preference for rizatriptan 10-mg wafer vs. eletriptan 40-mg tablet for acute treatment of migraine. Cephalalgia 2006 Mar; 26(3): 246–56
32.
Zurück zum Zitat Vollono C, Capuano A, Mei D, et al. Multiple attack study on the available triptans in Italy versus placebo. Eur J Neurol 2005 Jul; 12(7): 557–63PubMedCrossRef Vollono C, Capuano A, Mei D, et al. Multiple attack study on the available triptans in Italy versus placebo. Eur J Neurol 2005 Jul; 12(7): 557–63PubMedCrossRef
33.
Zurück zum Zitat Steiner TJ, Diener HC, MacGregor EA, et al. Comparative efficacy of eletriptan and zolmitriptan in the acute treatment of migraine. Cephalalgia 2003 Dec; 23(10): 942–52PubMedCrossRef Steiner TJ, Diener HC, MacGregor EA, et al. Comparative efficacy of eletriptan and zolmitriptan in the acute treatment of migraine. Cephalalgia 2003 Dec; 23(10): 942–52PubMedCrossRef
34.
Zurück zum Zitat Garcia-Ramos G, MacGregor EA, Hilliard B, et al. Comparative efficacy of eletriptan vs. naratriptan in the acute treatment of migraine. Cephalalgia 2003 Nov; 23(9): 869–76PubMedCrossRef Garcia-Ramos G, MacGregor EA, Hilliard B, et al. Comparative efficacy of eletriptan vs. naratriptan in the acute treatment of migraine. Cephalalgia 2003 Nov; 23(9): 869–76PubMedCrossRef
35.
Zurück zum Zitat Diener HC, Jansen JP, Reches A, et al. Efficacy, tolerability and safety of oral eletriptan and ergotamine plus caffeine (Cafergot®) in the acute treatment of migraine: a multicentre, randomised, double-blind, placebo-controlled comparison. Eur Neurol 2002; 47(2): 99–107PubMedCrossRef Diener HC, Jansen JP, Reches A, et al. Efficacy, tolerability and safety of oral eletriptan and ergotamine plus caffeine (Cafergot®) in the acute treatment of migraine: a multicentre, randomised, double-blind, placebo-controlled comparison. Eur Neurol 2002; 47(2): 99–107PubMedCrossRef
36.
Zurück zum Zitat Funk Orsini PA, Miceli RJ. Improvement in migraine-specific quality of life with eletriptan (Relpax™) vs Cafergot® [abstract no. P2-K61]. Cephalalgia 2001 May; 21: 431–2 Funk Orsini PA, Miceli RJ. Improvement in migraine-specific quality of life with eletriptan (Relpax™) vs Cafergot® [abstract no. P2-K61]. Cephalalgia 2001 May; 21: 431–2
37.
Zurück zum Zitat Funk Orsini PA, Miceli RJ. Comparison of the impact of eletriptan (Relpax™) and sumatriptan on migraine-specific quality of life [abstract no. P2-K62]. Cephalalgia 2001 May; 21: 432 Funk Orsini PA, Miceli RJ. Comparison of the impact of eletriptan (Relpax™) and sumatriptan on migraine-specific quality of life [abstract no. P2-K62]. Cephalalgia 2001 May; 21: 432
38.
Zurück zum Zitat Wells N, Hettiarachchi J, Drummond M, et al. A cost-effectiveness analysis of eletriptan 40 and 80 mg versus sumatriptan 50 and 100 mg in the acute treatment of migraine. Value Health 2003 Jul; 6(4): 438–47PubMedCrossRef Wells N, Hettiarachchi J, Drummond M, et al. A cost-effectiveness analysis of eletriptan 40 and 80 mg versus sumatriptan 50 and 100 mg in the acute treatment of migraine. Value Health 2003 Jul; 6(4): 438–47PubMedCrossRef
39.
Zurück zum Zitat Gracia-Naya M, Rejas Gutiérrez J, Latorre Jiménez A, et al. Economic evaluation of acute migraine attack treatment with triptans in Spain [in Spanish]. Neurologia 2005 Apr; 20(3): 121–32PubMed Gracia-Naya M, Rejas Gutiérrez J, Latorre Jiménez A, et al. Economic evaluation of acute migraine attack treatment with triptans in Spain [in Spanish]. Neurologia 2005 Apr; 20(3): 121–32PubMed
40.
Zurück zum Zitat Perfetto EM, Weis KA, Mullins CD, et al. An economic evaluation of triptan products for migraine. Value Health 2005 Nov–Dec; 8(6): 647–55PubMedCrossRef Perfetto EM, Weis KA, Mullins CD, et al. An economic evaluation of triptan products for migraine. Value Health 2005 Nov–Dec; 8(6): 647–55PubMedCrossRef
41.
Zurück zum Zitat Belsey JD. Cost effectiveness of oral triptan therapy: a transnational comparison based on a meta-analysis of randomised controlled trials. Curr Med Res Opin 2004 May; 20(5): 659–69PubMedCrossRef Belsey JD. Cost effectiveness of oral triptan therapy: a transnational comparison based on a meta-analysis of randomised controlled trials. Curr Med Res Opin 2004 May; 20(5): 659–69PubMedCrossRef
42.
Zurück zum Zitat Wells NEJ, Steiner TJ. Effectiveness of eletriptan in reducing time loss caused by migraine attacks. Pharmacoeconomics 2000 Dec; 18(6): 557–66PubMedCrossRef Wells NEJ, Steiner TJ. Effectiveness of eletriptan in reducing time loss caused by migraine attacks. Pharmacoeconomics 2000 Dec; 18(6): 557–66PubMedCrossRef
43.
Zurück zum Zitat Wells NEJ. The effectiveness of oral eletriptan (20–80 mg) at reducing the time loss associated with an acute migraine attack [abstract no. P05.138]. Neurology 2000 Apr 11; 54(7 Suppl. 3): 382 Wells NEJ. The effectiveness of oral eletriptan (20–80 mg) at reducing the time loss associated with an acute migraine attack [abstract no. P05.138]. Neurology 2000 Apr 11; 54(7 Suppl. 3): 382
44.
Zurück zum Zitat Wells NEJ. Comparison of the effectiveness of eletriptan, sumatriptan and Cafergot® in reducing the time loss associated with migraine attacks. J Drug Assess 2001; 4: 265–74 Wells NEJ. Comparison of the effectiveness of eletriptan, sumatriptan and Cafergot® in reducing the time loss associated with migraine attacks. J Drug Assess 2001; 4: 265–74
45.
Zurück zum Zitat McKenzie I, Pitman V. Safety, tolerability, and efficacy of eletriptan (40 mg–80 mg) for long-term treatment of migraine [abstract no. P 3054]. Eur J Neurol 2000 Nov; 7Suppl. 3: 118 McKenzie I, Pitman V. Safety, tolerability, and efficacy of eletriptan (40 mg–80 mg) for long-term treatment of migraine [abstract no. P 3054]. Eur J Neurol 2000 Nov; 7Suppl. 3: 118
Metadaten
Titel
Spotlight on Eletriptan in Migraine
verfasst von
Paul L. McCormack
Gillian M. Keating
Publikationsdatum
01.11.2006
Verlag
Springer International Publishing
Erschienen in
CNS Drugs / Ausgabe 11/2006
Print ISSN: 1172-7047
Elektronische ISSN: 1179-1934
DOI
https://doi.org/10.2165/00023210-200620110-00008

Weitere Artikel der Ausgabe 11/2006

CNS Drugs 11/2006 Zur Ausgabe

Adis Drug Evaluation

Varenicline

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Hirnblutung unter DOAK und VKA ähnlich bedrohlich

17.05.2024 Direkte orale Antikoagulanzien Nachrichten

Kommt es zu einer nichttraumatischen Hirnblutung, spielt es keine große Rolle, ob die Betroffenen zuvor direkt wirksame orale Antikoagulanzien oder Marcumar bekommen haben: Die Prognose ist ähnlich schlecht.

Thrombektomie auch bei großen Infarkten von Vorteil

16.05.2024 Ischämischer Schlaganfall Nachrichten

Auch ein sehr ausgedehnter ischämischer Schlaganfall scheint an sich kein Grund zu sein, von einer mechanischen Thrombektomie abzusehen. Dafür spricht die LASTE-Studie, an der Patienten und Patientinnen mit einem ASPECTS von maximal 5 beteiligt waren.

Schwindelursache: Massagepistole lässt Otholiten tanzen

14.05.2024 Benigner Lagerungsschwindel Nachrichten

Wenn jüngere Menschen über ständig rezidivierenden Lagerungsschwindel klagen, könnte eine Massagepistole der Auslöser sein. In JAMA Otolaryngology warnt ein Team vor der Anwendung hochpotenter Geräte im Bereich des Nackens.

Schützt Olivenöl vor dem Tod durch Demenz?

10.05.2024 Morbus Alzheimer Nachrichten

Konsumieren Menschen täglich 7 Gramm Olivenöl, ist ihr Risiko, an einer Demenz zu sterben, um mehr als ein Viertel reduziert – und dies weitgehend unabhängig von ihrer sonstigen Ernährung. Dafür sprechen Auswertungen zweier großer US-Studien.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.