Narcolepsy and pregnancy: a retrospective European evaluation of 249 pregnancies

In a retrospective cohort study undertaken in 12 European countries, 249 female narcoleptic patients with cataplexy (n = 216) and without cataplexy (n = 33) completed a self-administrated questionnaire regarding pregnancy and childbirth. The cohort was divided further into patients whose symptoms of narcolepsy started before or during pregnancy (308 pregnancies) and those in whom the first symptoms of narcolepsy appeared after delivery (106 pregnancies). Patients with narcolepsy during pregnancy were older during their first pregnancy (P < 0.001) and had a higher body mass index (BMI) prior to pregnancy (P < 0.01). Weight gain during pregnancy was higher in narcoleptic patients with cataplexy (P < 0.01). More patients with narcolepsy-cataplexy during pregnancy had impaired glucose metabolism and anaemia. Three patients experienced cataplexy during delivery. The rate of caesarean sections was higher in the narcolepsy-cataplexy group compared to the narcolepsy group (P < 0.05). The mean birth weight and gestational age of neonates were within the normal range and did not differ across groups. Neonatal care was affected adversely by symptoms of narcolepsy in 60.1% of those with narcolepsy during pregnancy. This study reports more obstetric complications in patients with narcolepsy-cataplexy during pregnancy; however, these were not severe. This group also had a higher BMI and higher incidence of impaired glucose metabolism during pregnancy. Caesarian section was conducted more frequently in narcolepsy-cataplexy patients, despite cataplexy being a rare event during delivery. Furthermore, symptoms of narcolepsy may render care of the infant more difficult.

Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study

The aim of this study was to describe the clinical and PSG characteristics of narcolepsy with cataplexy and their genetic predisposition by using the retrospective patient database of the European Narcolepsy Network (EU-NN). We have analysed retrospective data of 1099 patients with narcolepsy diagnosed according to International Classification of Sleep Disorders-2. Demographic and clinical characteristics, polysomnography and multiple sleep latency test data, hypocretin-1 levels, and genome-wide genotypes were available. We found a significantly lower age at sleepiness onset (men versus women: 23.74 ± 12.43 versus 21.49 ± 11.83, P = 0.003) and longer diagnostic delay in women (men versus women: 13.82 ± 13.79 versus 15.62 ± 14.94, P = 0.044). The mean diagnostic delay was 14.63 ± 14.31 years, and longer delay was associated with higher body mass index. The best predictors of short diagnostic delay were young age at diagnosis, cataplexy as the first symptom and higher frequency of cataplexy attacks. The mean multiple sleep latency negatively correlated with Epworth Sleepiness Scale (ESS) and with the number of sleep-onset rapid eye movement periods (SOREMPs), but none of the polysomnographic variables was associated with subjective or objective measures of sleepiness. Variant rs2859998 in UBXN2B gene showed a strong association (P = 1.28E-07) with the age at onset of excessive daytime sleepiness, and rs12425451 near the transcription factor TEAD4 (P = 1.97E-07) with the age at onset of cataplexy. Altogether, our results indicate that the diagnostic delay remains extremely long, age and gender substantially affect symptoms, and that a genetic predisposition affects the age at onset of symptoms.

ImmunoChip study implicates antigen presentation to T cells in narcolepsy

Recent advances in the identification of susceptibility genes and environmental exposures provide broad support for a post-infectious autoimmune basis for narcolepsy/hypocretin (orexin) deficiency. We genotyped loci associated with other autoimmune and inflammatory diseases in 1,886 individuals with hypocretin-deficient narcolepsy and 10,421 controls, all of European ancestry, using a custom genotyping array (ImmunoChip). Three loci located outside the Human Leukocyte Antigen (HLA) region on chromosome 6 were significantly associated with disease risk. In addition to a strong signal in the T cell receptor alpha (TRA@), variants in two additional narcolepsy loci, Cathepsin H (CTSH) and Tumor necrosis factor (ligand) superfamily member 4 (TNFSF4, also called OX40L), attained genome-wide significance. These findings underline the importance of antigen presentation by HLA Class II to T cells in the pathophysiology of this autoimmune disease.

Exposure dating of Late Glacial and pre-LGM moraines in the Cordon de Doña Rosa, Northern/Central Chile (~ 31°S)

Despite the important role of the Central Andes (15–30° S) for climate reconstruction, knowledge about the Quaternary glaciation is very limited due to the scarcity of organic material for radiocarbon dating. We applied 10Be surface exposure dating (SED) on 22 boulders from moraines in the Cordon de Doña Rosa, Northern/Central Chile (~31° S). The results show that several glacial advances in the southern Central Andes occurred during the Late Glacial between ~14.7±1.5 and 11.6±1.2 ka. A much more extensive glaciation is dated to ~32±3 ka, predating the temperature minimum of the global LGM (Last Glacial Maximum: ~20 ka). Reviewing these results in the paleoclimatic context, we conclude that the Late Glacial advances were most likely caused by an intensification of the tropical circulation and a corresponding increase in summer precipitation. High-latitude temperatures minima, e.g. the Younger Dryas (YD) and the Antarctic Cold Reversal (ACR) may have triggered individual advances, but current systematic exposure age uncertainties limit precise correlations. The absence of LGM moraines indicates that moisture advection was too limited to allow significant glacial advances at ~20 ka. The tropical circulation was less intensive despite the maximum in austral summer insolation. Winter precipitation was apparently also insufficient, although pollen and marine studies indicate a northward shift of the westerlies at that time. The dominant pre-LGM glacial advances in Northern/Central Chile at ~32 ka required lower temperatures and increased precipitation than today. We conclude that the westerlies were more intense and/or shifted equatorward, possibly due to increased snow and ice cover at higher southern latitudes coinciding with a minimum of insolation.

Geballte Faust, Doppelaxt, rosa Winkel. Gruppenkonstituierende Symbole der Frauen-, Lesben- und Schwulenbewegung

2008 jährte sich die Zäsur von 1968 zum 40. Mal. Besonders an diesem Jahrestag war, dass nun die nächste Generation in die gesellschaftliche Reflexion eingetreten ist. Das aus Vertretern der nach 1968 Geborenen bestehende Schweizer Ausstellungsbüro Palma3 hat aus diesem Anlass gemeinsam mit dem Historischen Museum in Frankfurt am Main die Ausstellung „Die 68er. Kurzer Sommer – lange Wirkung“ realisiert. Im Rahmen von acht Themenbereichen, die die wichtigsten Aufbrüche von 1968 und ihre Weiterentwicklung in den 1970er Jahren dokumentieren und reflektieren, nahm der Bereich „Geschlechterrollen“ einen besonderen Raum ein. Er präsentierte materialreich die Frauen-, Lesben- und Schwulenbewegung sowie die so genannte sexuelle Revolution der 1960er und 1970er Jahre in der Bundesrepublik Deutschland in ihren spannungsvollen Wechselverhältnissen. Im Zentrum des Beitrages sollen die unterschiedlichen Symbole dieser Bewegungen stehen. Diese dokumentieren anschaulich das Aushandeln gruppenkonstituierender Identitäten, wobei Rückgriffe auf ältere Symbole und deren Transformationen sowie Neukontextualisierungen zu beobachten sind. In der Frauenbewegung war das Venus-/Weiblichkeitszeichen mit geballter Faust im Innern in verschiedenen Versionen als grafische Verbindung von linker Bewegung und Feminismus verbreitet. Zwei ineinander verschlungene Weiblichkeitssymbole stehen in der Lesbenbewegung für weib-weibliche Sexualität. Dass die Frauen- und die Lesbenbewegung teilweise eine enge Allianz eingegangen sind, lässt sich auch an ihren gemeinsamen Symbolen ablesen: Die Labrys (Doppelaxt), eine minoische Kultaxt, repräsentiert die Autonomie und Stärke der Amazonen, als deren Waffe sie gilt. Das alte Zeichen der beiden gegeneinander gestellten Hände stellt eine Vagina dar und wurde ursprünglich von Männern als obszöne Geste für den Geschlechtsverkehr benutzt, wobei die Hände in Höhe ihrer Geschlechtsorgane gehalten wurden. In der Frauen- und Lesbenbewegung wurde dieses Zeichen mit erhobenen Armen über dem Kopf gezeigt, um die sexuelle Selbstbestimmung der Frauen deutlich zu machen. Demgegenüber greift die Schwulenbewegung auf den rosa Winkel als Symbol zurück. Dieser kennzeichnete während des Nationalsozialismus’ männliche Häftlinge in Konzentrationslagern als homosexuell. Er wurde von der deutschen Schwulenbewegung aufgegriffen und in emanzipatorischer Absicht umgewertet, wobei die nationalsozialistische Vergangenheit des Symbols präsent bleiben sollte. Insbesondere in den frühen 1970er Jahren finden sich unterschiedlichste Entwürfe dieser Symbole auf Flugblättern, Broschüren, Zeitschriften, Büchern, Plakaten und Transparenten. An Hand einzelner Gruppierungen wie der Homosexuellen Aktion Westberlin, die als Schwulen- und Lesbenorganisation gegründet worden war, sich jedoch schnell in die HAW und das LAZ (LesbenAktionsZentrum) aufsplittete, der Frauenorganisation Brot und Rosen und der Roten Zelle Schwul (ROTZSCHWUL) soll der Aushandlungsprozess innerhalb der Gruppierungen sowie das Verhandeln von Gruppenidentität und -inszenierung nach innen und außen nachgezeichnet werden. Zugleich lässt sich das Weiterexistieren bzw. Verschwinden der jeweiligen Symbole wie auch das Entstehen neuer Symbole – beispielsweise der Regenbogenfahne – als Indiz für die Veränderungen innerhalb der Bewegungen und deren Selbstwahrnehmung und Selbstinszenierung lesen.

DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe

STUDY OBJECTIVE Prior research has identified five common genetic variants associated with narcolepsy with cataplexy in Caucasian patients. To replicate and/or extend these findings, we have tested HLA-DQB1, the previously identified 5 variants, and 10 other potential variants in a large European sample of narcolepsy with cataplexy subjects. DESIGN Retrospective case-control study. SETTING A recent study showed that over 76% of significant genome-wide association variants lie within DNase I hypersensitive sites (DHSs). From our previous GWAS, we identified 30 single nucleotide polymorphisms (SNPs) with P < 10(-4) mapping to DHSs. Ten SNPs tagging these sites, HLADQB1, and all previously reported SNPs significantly associated with narcolepsy were tested for replication. PATIENTS AND PARTICIPANTS For GWAS, 1,261 narcolepsy patients and 1,422 HLA-DQB1*06:02-matched controls were included. For HLA study, 1,218 patients and 3,541 controls were included. MEASUREMENTS AND RESULTS None of the top variants within DHSs were replicated. Out of the five previously reported SNPs, only rs2858884 within the HLA region (P < 2x10(-9)) and rs1154155 within the TRA locus (P < 2x10(-8)) replicated. DQB1 typing confirmed that DQB1*06:02 confers an extraordinary risk (odds ratio 251). Four protective alleles (DQB1*06:03, odds ratio 0.17, DQB1*05:01, odds ratio 0.56, DQB1*06:09 odds ratio 0.21, DQB1*02 odds ratio 0.76) were also identified. CONCLUSION An overwhelming portion of genetic risk for narcolepsy with cataplexy is found at DQB1 locus. Since DQB1*06:02 positive subjects are at 251-fold increase in risk for narcolepsy, and all recent cases of narcolepsy after H1N1 vaccination are positive for this allele, DQB1 genotyping may be relevant to public health policy.