Patients with visual snow (VS) describe tiny flickering dots in the entire visual field often compared with the TV static in case of a badly adjusted analog signal. It can be episodic with migraine , but is debilitating when continuously present. When occurring together with visual (palinopsia, enhanced entoptic phenomena, photophobia, and nyctalopia) and a variety of non-visual symptoms (tinnitus, concentration loss, etc.), one speaks of visual snow syndrome (VSS) .
Pathophysiological mechanisms are still not well-understood, and pharmacological treatment options are sparse. We present a case of VSS onset after citalopram intake and discuss this constellation in the light of “Hallucinogen Persisting Perception Disorder” (HPPD) with possible shared receptor mechanisms.
Two weeks after starting with citalopram 20 mg to treat postpartum depression, a 31-year-old female developed visual disturbances in terms of white and black dots in the entire visual field, intermittent bright flashes, entoptic phenomena, swirls, photophobia, and additionally increased irritability to external sensory cues. Past medical history was unremarkable except for episodic migraine without aura (every 8 weeks; MIDAS 0p). There was moderate anxiety and depression as assessed by the GAD-7 anxiety scale (7p) and the PHQ-9 depression scale (10p) at that time. There was no use of hallucinogenic substances in the past. Diagnostics including thorough clinical neurological and ophthalmological examination, visual evoked potentials (16 k and 64 k), and MRI-scan of the brain were unremarkable. VSS persisted after stopping citalopram. An additionally used causality assessment tool (CAT) for adverse drug reaction (ADR), namely the Liverpool ADR CAT, indicated a possible adverse drug reaction .
Individual symptoms of VSS can overlap with conditions such as visual migraine aura [2, 4] and HPPD [5, 6]. Particularly, VSS and HPPD symptoms largely overlap and therefore might share common pathophysiological mechanisms in terms of involved cerebral networks and changes in synaptic transmission. The drug lysergic acid diethylamide (LSD) mediates its hallucinogenic effects mainly via activating the serotonergic 5HT2a-receptor . Even one-time consumption of LSD can cause persistent HPPD with VS-like symptoms . Interestingly, there are reports on visual sensations arising years after LSD abuse triggered by the intake of selective serotonin reuptake inhibitors (SSRI) in patients with former HPPD . Regarding our case, the hypothesis arises that changes in serotonergic synaptic transmission, particularly via 5HT2a-receptors, in primary and/or secondary visual cortical areas might underlie VSS as well as HPPD. Functional imaging studies revealed increased metabolism in secondary visual cortical areas such as the lingual gyrus in VSS . There is evidence for a particularly high density of 5HT2-receptors of projections from the lateral geniculate body of the thalamus to the primary visual cortex [8, 9]. It is hypothesized that a shift in the balance of excitatory and inhibitory synaptic transmission in the visual cortex towards more excitation due to a decrease in either the number or the functional activation of inhibitory serotonergic interneurons might play a crucial role in HPPD after LSD abuse . Thus, in subjects with an increased vulnerability, VSS might also be triggered by minor changes in serotonergic transmission due to SSRI, like in our case. Further evidence for the important role of serotonergic transmission derives from the at least partial effectiveness of lamotrigine in both conditions [10,11,12], as lamotrigine also has an inhibitory function on 5HT2a-receptors .
This case report gives further insight for a possible role of changes in serotonergic transmission in brain regions important for visual processing as potentially underlying pathophysiological mechanism of VSS. Furthermore, common pathophysiological changes in VSS and HPPD on the level of cerebral network activations and synaptic transmission seem plausible.
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Hodak J, Fischer U, Bassetti CLA, Schankin CJ (2019) Episodic visual snow associated with migraine attacks. JAMA Neurol 77:392–393. https://doi.org/10.1001/jamaneurol.2019.4050
Schankin C, Maniyar FH, Digre KB, Goadsby PJ (2014) “Visual snow” - a disorder distinct from persistent migraine aura. Brain 137:1419–1428. https://doi.org/10.1093/brain/awu050
Gallagher RM, Kirkham JJ, Mason JR, Bird KA, Williamson PR, Nunn AJ, Turner MA, Smyth RL, Pirmohamed M (2011) Development and inter-rater reliability of the Liverpool adverse drug reaction causality assessment tool. PLoS One 6:e28096. https://doi.org/10.1371/journal.pone.0028096
Schankin CJ, Maniyar FH, Sprenger T, Chou DE, Eller M, Goadsby PJ (2014) The relation between migraine, typical migraine aura and “visual snow.”. Headache 54:957–966. https://doi.org/10.1111/head.12378
Halpern JH, Pope HG (2003) Hallucinogen persisting perception disorder: what do we know after 50 years? Drug Alcohol Depend 69:109–119. https://doi.org/10.1016/S0376-8716(02)00306-X
Abraham HD, Aldridge AM, Gogia P (1996) The psychopharmacology of hallucinogens. Neuropsychopharmacology 14:285–298. https://doi.org/10.1016/0893-133X(95)00136-2
Goldman S, Galarneau D, Friedman R (2007) New onset LSD flashback syndrome triggered by the initiation of SSRIs. Ochsner J 7:37–39
Pazos A, González AM, Waeber C, Palacios JM (1991) Chapter 4 - multiple serotonin receptors in the human brain. In: Mendelsohn FAO, Paxinos G (eds) Receptors in the human nervous system. Academic Press, pp 71–101
Burnet PWJ, Eastwood SL, Lacey K, Harrison PJ (1995) The distribution of 5-HT1A and 5-HT2A receptor mRNA in human brain. Brain Res 676:157–168. https://doi.org/10.1016/0006-8993(95)00104-X
Rothrock JF (1997) Successful Treatment of Persistent Migraine Aura with Divalproex Sodium. Neurology 48:261–262. https://doi.org/10.1212/WNL.48.1.261
Unal-Cevik I, Yildiz FG (2015) Visual snow in migraine with aura: further characterization by brain imaging, electrophysiology, and treatment – case report. Headache 55:1436–1441. https://doi.org/10.1111/head.12628
Martinotti G, Santacroce R, Pettorruso M, Montemitro C, Spano M, Lorusso M, di Giannantonio M, Lerner A (2018) Hallucinogen persisting perception disorder: etiology, clinical features, and therapeutic perspectives. Brain Sci 8:. https://doi.org/10.3390/brainsci8030047
Wishart DS, Feunang YD, Guo AC, Lo EJ, Marcu A, Grant JR, Sajed T, Johnson D, Li C, Sayeeda Z, Assempour N, Iynkkaran I, Liu Y, Maciejewski A, Gale N, Wilson A, Chin L, Cummings R, le D, Pon A, Knox C, Wilson M (2018) DrugBank 5.0: a major update to the DrugBank database for 2018. Nucleic Acids Res 46:D1074–D1082. https://doi.org/10.1093/nar/gkx1037
Conflict of interest
OE Eren has received honoraria for consulting within the past three years from Novartis Pharma. FS has nothing to report. CJ Schankin has received honoraria for consulting and lectures within the past 3 years from Novartis, Eli Lilly, Allergan, Almirall, Amgen, Teva Pharmaceuticals, MindMed, and Grünenthal outside the submitted work. AS has received honoraria for consulting and lectures within the past 3 years from Allergan Pharma, Bayer, Lilly, Novartis Pharma, Sanofi, and TEVA.
The work was conducted in accordance with the Declaration of Helsinki and approved by the ethics committee of the Ludwig Maximilians University Munich (227-15). The subject was recruited between 2015 and 2017 and gave written informed consent.
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Eren, O.E., Schöberl, F., Schankin, C.J. et al. Visual snow syndrome after start of citalopram—novel insights into underlying pathophysiology. Eur J Clin Pharmacol 77, 271–272 (2021). https://doi.org/10.1007/s00228-020-02996-9