Best practice guidelines on first-line laboratory testing for porphyria. (March 2017)

• Record Type: Journal Article
• Authors: Woolf, Jacqueline; Marsden, Joanne T; Degg, Timothy; Whatley, Sharon; Reed, Paul; Brazil, Nadia; Stewart, M Felicity; Badminton, Michael
• Is Part Of: Annals of clinical biochemistry. Volume 54:Number 2(2017:Mar.)
• Page Start: 188
• Page End: 198
• Publication Date: 2017-03
• Subjects: Inborn errors of metabolism -- clinical studies -- fluorometry -- laboratory methods -- colourimetry; Clinical chemistry -- Periodicals; Clinical biochemistry -- Periodicals; 616.075
• DOI: 10.1177/0004563216667965
• Languages: English
• ISSNs: 0004-5632

Abstract

The porphyrias are disorders of haem biosynthesis which present with acute neurovisceral attacks or disorders of sun-exposed skin. Acute attacks occur mainly in adults and comprise severe abdominal pain, nausea, vomiting, autonomic disturbance, central nervous system involvement and peripheral motor neuropathy. Cutaneous porphyrias can be acute or chronic presenting at various ages. Timely diagnosis depends on clinical suspicion leading to referral of appropriate samples for screening by reliable biochemical methods. All samples should be protected from light. Investigation for an acute attack: Porphobilinogen (PBG) quantitation in a random urine sample collected during symptoms. Urine concentration must be assessed by measuring creatinine, and a repeat requested if urine creatinine <2 mmol/L. Urgent porphobilinogen testing should be available within 24 h of sample receipt at the local laboratory. Urine porphyrin excretion (TUP) should subsequently be measured on this urine. Urine porphobilinogen should be measured using a validated quantitative ion-exchange resin-based method or LC-MS. Increased urine porphobilinogen excretion requires confirmatory testing and clinical advice from the National Acute Porphyria Service. Identification of individual acute porphyrias requires analysis of urine, plasma and faecal porphyrins. Investigation for cutaneous porphyria: An EDTA blood sample for plasma porphyrin fluorescence emission spectroscopy and random urine sample for TUP. Whole blood for porphyrin analysis is essential to identify protoporphyria. Faeces need only be collected, if first-line tests are positive or if clinical symptoms persist. Investigation for latent porphyria or family history: Contact a specialist porphyria laboratory for advice. Clinical, family details are usually required.