To the Editor:
While gout is a very common and well-described disorder, it is rarely diagnosed in a young, premenopausal woman1. Overall, men are more than twice as likely to develop this condition over their lifetime as women. This sex difference is at its greatest in the 20- to 49-year age group, where incidence is 1.3% for men versus 0.4% for women2,3. The lower prevalence and incidence of gout in women has been attributed to the protective effects of estrogen and menstruation, which is consistent with the observation that it commonly manifests in women 10 to 15 years after menopause. When gout occurs in men under 30 years or in young women, investigation for a secondary cause is recommended4. This investigation should include checking for acquired risk factors and genetic disorders that exacerbate hyperuricemia (Table 1).
A 27-year-old woman was referred by a nephrologist for chronic and intermittent right first toe pain, redness, and swelling for the past year. It was exacerbated by tight shoes, and relieved with nonsteroidal antiinflammatory drugs (NSAID). She also reported several episodes of pain, swelling, and redness in both ankles over the past year. She was constitutionally well and denied fevers, weight loss, or night sweats. Further history revealed psoriasis (PsO) treated with ultraviolet light therapy. She reported heavy alcohol use over the past 3 to 4 years, with binge drinking, and was previously hospitalized for acute pancreatitis. More recently she was diagnosed with Gitelman syndrome upon presenting with 2 years of episodically elevated creatinine along with hyponatremia, hypokalemia, elevated bicarbonate, and borderline high calcium. A diagnosis of Gitelman syndrome was made by exclusion of other conditions causing electrolyte imbalance and metabolic alkalosis, such as primary hyperaldosteronism, vomiting, and drugs (diuretics or laxatives). Her bland urinalysis, normal renal ultrasound, and no family history of renal disease further helped rule out glomerular, parenchymal, and other genetic causes. Her electrolyte abnormalities were managed with fluid and electrolyte replacement.
Given that Gitelman syndrome follows an autosomal recessive genetic pattern, it was hypothesized that both her parents were likely carriers. Confirmatory genetic testing was not performed for a number of reasons; the large number of involved genes and mutations, familial genetic heterogeneity, and high cost all limit the practicality of a molecular diagnostic approach5.
On examination, the patient was noted to be of a healthy body mass index. Musculoskeletal examination revealed 1 tender and swollen joint [right first metatarsophalangeal (MTP)] and restricted range of motion. The ankles were mildly restricted bilaterally, but no other joint swelling or tenderness was noted. Skin examination revealed psoriatic plaques over the elbows, knees, and shins.
On presentation to the rheumatology clinic, blood work revealed normal electrolytes and serum creatinine 83 µmol/l; however, previous creatinine levels ranged from 66 to 194 µmol/l. Uric acid (UA) was significantly elevated at 759 µmol/l. Liver enzyme were abnormal: aspartate aminotransferase 110 U/l, alanine aminotransferase 137 U/l, alkaline phosphatase 172 U/l, and γ-glutamyl transferase 91 U/l.
Synovial fluid aspiration of the first MTP joint revealed chalky white material, with UA crystals on polarized microscopy. The joint was injected with corticosteroids and the patient was instructed to stop all alcohol intake and NSAID use. At followup 2 weeks later, she reported significant improvement in pain and swelling, and cessation of alcohol intake resulted in normalization of liver enzymes. Her UA remained elevated at 759 µmol/l. Given the tophaceous gout tophus deposit and recurrent joint symptoms, UA-lowering therapy with febuxostat 80 mg daily plus colchicine 0.6 mg bid was initiated. One year later, she was asymptomatic with no recurrence of gouty flares, her UA level decreased to 141 µmol/l, and creatinine was 65 µmol/l.
Our patient was diagnosed with Gitelman syndrome, a rare autosomal recessive inherited renal tubular defect (prevalence estimated at 1:40,000). The clinical presentation is known to mimic the effects of a thiazide diuretic with a defect in the thiazide-sensitive sodium chloride cotransporter (NCCT) in the renal distal convoluted tubule5,6. Sodium-chloride reabsorption is impaired leading to salt loss and reduced circulating volume, activating the renin-angiotensin-aldosterone system (RAAS) leading to hypokalemia and hypochloremic metabolic alkalosis7. Thiazide diuretics are known to increase serum UA levels8. Similarly, dietary salt restriction has been shown to increase uric acid concentrations, perhaps by altering renal tubular function9,10. However, to our knowledge there is no literature describing an association between Gitelman syndrome and gout, and therefore it is unclear what levels of serum UA would be expected in this syndrome.
Historically, it has been accepted that thiazide diuretics increase net UA reabsorption indirectly through diuretic-induced volume depletion and activation of the RAAS system8,11. More recent data suggest diuretics have a direct interaction on renal UA handling through the voltage-driven UA transporter hNPT4/SLC17A312, as well as the cyclic nucleotide transporter, MRP4/ABCC413. Interestingly, Gitelman syndrome has recently been described as associated with mutations in the UA transporter gene, SLC17A314. A detailed mechanism of thiazide diuretic effect on renal handling of UA is depicted in Figure 1. These findings along with clinical observations in our case report support a potential novel mechanism for the effect of Gitelman syndrome on tubular UA transport that would be the cause of its association with hyperuricemia.
Gout is most commonly seen in older men and postmenopausal women, and has well-described risk factors. It is uncharacteristic to observe tophaceous gout in a young woman, a clinical presentation that should prompt rheumatologists to investigate a secondary cause. In our patient, there were many contributing factors that drove elevated UA levels and clinical development of tophaceous gout. Her risk factors included the thiazide-like effect of Gitelman syndrome, along with excess alcohol use, acute renal failure, and increased cell turnover from PsO. She was managed with UA-lowering therapy and modification of lifestyle, including cessation of alcohol and NSAID use. The target level of UA was achieved, an important goal to prevent future joint symptoms and damage.
To our knowledge, our case study highlights for the first time the association between Gitelman syndrome and gout. We identified Gitelman syndrome as a novel risk factor for the development of gout and provided early insights into the pathogenesis of its association with hyperuricemia. However, further investigation is warranted into the pathogenesis of Gitelman syndrome, hyperuricemia, and this association.
Research ethics board approval was not required for the publication of this case report.
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