Many obese patients share with patients suffering from idiopathic intracranial hypertension (IIH) increased intracranial pressure [1] and weight increase [2,3]. Obese patients have been reported to display signs of low-grade inflammation [1,4] and haemostatic changes [5][6][7]. Such markers have not been much examined in IIH.This study investigated markers of inflammation and haemostasis in IIH patients with bilateral papilledema and healthy age-and sex-matched controls with body mass index (BMI) below 25. As normal values for cerebrospinal fluid pressure (Pcsf) are not distinct, (150 ± 50 mm water in nonobese and up to 250 mm water in obese [8]), only IIH patients with bilateral papilledema, i.e., with Pcsf above 350 mm water [9], were recruited for our study. As low-grade systemic inflammation in IIH may escape detection if normal values of inflammation markers were used for comparison to the findings in IIH patients, only a well-defined group of healthy, age-and sex-matched persons could be used as controls. The controls had to have BMI below 25, as some, but not all [10], overweight and obese patients display intracranial hypertension, signs of inflammation and haemostatic abnormalities and consequently could not be used for comparison [1,[5][6][7].The laboratory tests performed were considered to best reflect the presence of signs of inflammation and coagulopathies. Inflammation markers were fibrinogen, C-reactive protein (CRP) haptoglobin, orosomucoid, immunoglobulins G and M earlier found to be increased in overweight and obese patients [1,4]. Of the analysed haemostatic markers, von Willebrand factor antigen and plasminogen activator inhibitor (PAI-1) have been considered also to reflect inflammation. The other haemostatic markers studied were overall haemostatic potential (OHP), overall coagulation potential (OCP), overall fibrinolysis potential (OFP), thrombin-antithrombin complex, prothrombin fragment 1 + 2, fibrin-d-dimer, von Willebrand factor antigen, von Willebrand ristocetin cofactor, and the inhibitors protein C, protein S, and lupus anticoagulant. (OHP summarizes coagulation and fibrinolytic activations in one assay, OCP, if increased, indicates hypercoagulation, and OFP changes as to fibrinolysis.)For further markers of inflammation, six of the IIH patients and eight of the controls were investigated as to expression of tumour necrosis factor-a, interleukins 2, 6, 10, 23 (IL-2, IL-6, IL-10, IL-23) and Fox P3 in peripheral mononuclear (PBMC) and cerebrospinal fluid (csf) cells.