13 research outputs found
Treatment of Iron-deficiency Anemia in Patients with Subclinical Hypothyroidism
Subclinical hypothyroidism is a health state that is associated with hypercholesterolemia,
infertility, iron-deficiency anemia, and poor obstetric outcome. This article summarizes the results of a
prospective clinical investigation of whether treatment of subclinical hypothyroidism and iron-deficiency
anemia with a combination of levothyroxine plus iron salt would be superior to each treatment alone
Adrenal Vein Cortisol to Metanephrine Ratio for Localizing ACTH-Independent Cortisol-Producing Adenoma: A Case Report
Context: Finding the source of adrenocorticotropic hormone (ACTH)-independent cortisol-producing adenoma in the patients with subclinical Cushing syndrome (SCS) and bilateral adrenal nodules is sometimes challenging. Computed tomography (CT) and positron emission tomography are helpful, but adrenal venous sampling (AVS) is the gold standard approach. However, interpretation of AVS is important to improve the accuracy of decision-making for surgery. We report a case and review of the literature to assess the benefit of using adrenal vein cortisol to metanephrine ratio to determine the source of cortisol production in SCS and bilateral nodules.
Evidence Acquisition: Three authors searched PubMed for data on patients with SCS who had AVS procedure and measurements of cortisol and catecholamines.
Case Description: A 51-year-old woman with SCS and hypertension crisis presented to our clinic. Paraclinical investigations revealed that she had an ACTH-independent cortisol-producing adenoma and her CT scan showed bilateral adrenal nodules. After AVS, cortisol (high to low) lateralization ratio could not determine the source of cortisol production but the cortisol to metanephrine ratio localized the source to the left side, which included the larger nodule according to CT measurements. Left adrenalectomy led to clinical and paraclinical improvement.
Conclusion: There is a possibility of co-secretion of other steroids accompanied with cortisol in the setting of ACTH-independent SCS. Moreover, cortisol measurement alone and interpretation of AVS results based on cortisol values may not help lateralizing the source of cortisol production with bilateral adrenal nodules. Therefore, we suggest applying cortisol to metanephrine ratio with the same gradient (gradient \u3e 2.3, highest to lowest concentration) when the source of cortisol production cannot be determined by cortisol lateralization ratio
Bone Quality in Chronic Kidney Disease Patients: Current Concepts and Future Directions – Part II
Background: Patients with chronic kidney disease (CKD) have an increased risk of osteoporotic fractures, which is due not only to low bone volume and mass but also poor microarchitecture and tissue quality. The pharmacological and nonpharmacological interventions detailed, herein, are potential approaches to improve bone health in CKD patients. Various medications build up bone mass but also affect bone tissue quality. Antiresorptive therapies strikingly reduce bone turnover; however, they can impair bone mineralization and negatively affect the ability to repair bone microdamage and cause an increase in bone brittleness. On the other hand, some osteoporosis therapies may cause a redistribution of bone structure that may improve bone strength without noticeable effect on BMD. This may explain why some drugs can affect fracture risk disproportionately to changes in BMD. Summary: An accurate detection of the underlying bone abnormalities in CKD patients, including bone quantity and quality abnormalities, helps in institution of appropriate management strategies. Here in this part II, we are focusing on advancements in bone therapeutics that are anticipated to improve bone health and decrease mortality in CKD patients. Key Messages: Therapeutic interventions to improve bone health can potentially advance life span. Emphasis should be given to the impact of various therapeutic interventions on bone quality
Bone Quality in CKD Patients: Current Concepts and Future Directions – Part I
Background: There is ample evidence that patients with CKD have an increased risk of osteoporotic fractures. Bone fragility is not only influenced by low bone volume and mass but also by poor microarchitecture and tissue quality. More emphasis has been given to the quantitative rather than qualitative assessment of bone health, both in general population and CKD patients. Although bone mineral density (BMD) is a very useful clinical tool in assessing bone strength, it may underestimate the fracture risk in CKD patients. Serum and urinary bone biomarkers have been found to be reflective of bone activities and predictive of fractures independently of BMD in CKD patients. Bone quality and fracture risk in CKD patients can be better assessed by utilizing new technologies such as trabecular bone score and high-resolution imaging studies. Additionally, invasive assessments such as bone histology and micro-indentation are useful counterparts in the evaluation of bone quality. Summary: A precise diagnosis of the underlying skeletal abnormalities in CKD patients is crucial to prevent further bone loss and fractures. We must consider bone quantity and quality abnormalities for management of CKD patients. Here in this part I, we are focusing on advances in bone quality diagnostics that are expected to help in proper understanding of the bone health in CKD patients. Key Messages: Assessment of bone quality and quantity in CKD patients is essential. Both noninvasive and invasive techniques for the assessment of bone quality are available
Omentin-1, visfatin and adiponectin levels in relation to bone mineral density in Iranian postmenopausal women
The potential link between infection with Chlamydia
pneumoniae or Helicobacter pylori and osteoporosis
has not been investigated in population-based longitudinal
studies. A total of 250 healthy postmenopausal women
who participated in a prospective cohort study were evaluated
for IgG antibodies directed against C. pneumoniae and
H. pylori, osteoprotegerin (OPG), the receptor activator of
nuclear factor kappa B ligand (RANKL), CrossLaps, and
osteocalcin. Bone mineral density (BMD) was measured at
the femoral neck and lumbar spine at baseline and at follow-
up 5.8 years later. There were no significant differences
in age-adjusted bone turnover markers, OPG, RANKL,
the RANKL/OPG ratio, and BMD between the C. pneumoniae
and H. pylori IgG seropositive and seronegative
subjects (P > 0.05). Neither C. pneumoniae nor H. pylori
IgG seropositivity was associated with age-and body massindex-adjusted BMD at the femoral neck and lumbar spine
or bone loss at the 5.8-year follow-up. In logistic regression
analysis, neither C. pneumoniae nor H. pylori IgG seropositivities
predicted incident lumbar or spine osteoporosis
5.8 years later. In conclusion, neither C. pneumoniae nor
H. pylori IgG seropositivity was associated with bone turnover
markers, the RANKL/OPG ratio, BMD, or bone loss
in postmenopausal women. In addition, chronic infection
with C. pneumoniae or H. pylori did not predict incident
osteoporosis among this group of women
Chlamydia pneumoniae and Helicobacter pylori IgG seropositivities are not predictors of osteoporosis‑associated bone loss: a prospective cohort study
The potential link between infection with Chlamydia
pneumoniae or Helicobacter pylori and osteoporosis
has not been investigated in population-based longitudinal
studies. A total of 250 healthy postmenopausal women
who participated in a prospective cohort study were evaluated
for IgG antibodies directed against C. pneumoniae and
H. pylori, osteoprotegerin (OPG), the receptor activator of
nuclear factor kappa B ligand (RANKL), CrossLaps, and
osteocalcin. Bone mineral density (BMD) was measured at
the femoral neck and lumbar spine at baseline and at follow-up
5.8 years later. There were no significant differences
in age-adjusted bone turnover markers, OPG, RANKL,
the RANKL/OPG ratio, and BMD between the C. pneumoniae
and H. pylori IgG seropositive and seronegative
subjects (P > 0.05). Neither C. pneumoniae nor H. pylori
IgG seropositivity was associated with age-and body mass
index-adjusted BMD at the femoral neck and lumbar spine
or bone loss at the 5.8-year follow-up. In logistic regression
analysis, neither C. pneumoniae nor H. pylori IgG seropositivities predicted incident lumbar or spine osteoporosis 5.8 years later. In conclusion, neither C. pneumoniae nor H. pylori IgG seropositivity was associated with bone turnover markers, the RANKL/OPG ratio, BMD, or bone loss
in postmenopausal women. In addition, chronic infection
with C. pneumoniae or H. pylori did not predict incident
osteoporosis among this group of women.
Keywords Chlamydia pneumoniae · Helicobacter
pylori · Bone mineral density · Osteoporosi
Reduced serum osteocalcin concentrations are associated with type 2 diabetes mellitus and the metabolic syndrome components in postmenopausal women: the crosstalk between bone and energy metabolism
Although it has been shown that osteocalcin
functions as a hormone in the regulation of glucose
metabolism and fat mass, no population-based study to date
has addressed serum osteocalcin levels in relation to energy
metabolism concurrent with bone metabolism in postmenopausal
women. In a population-based study, cardiovascular
risk factors, high-sensitivity C-reactive protein
(hs-CRP), osteoprotegerin, receptor activator of nuclear
factor-jB ligand, osteocalcin, CrossLaps, alkaline phosphatase,
and bone mineral density (BMD) at the lumbar
spine (L2–L4) and the proximal femur were measured in
382 Iranian postmenopausal women. In multiple logistic
regression analysis, lower osteocalcin and CrossLaps levels
were associated with a higher odds ratio (OR) of having
type 2 diabetes mellitus when adjustments were made for
age, hs-CRP, cardiovascular risk factors, BMD, and
markers of bone metabolism [OR 5.17, CI (2.66–10.04),
p\0.0001 and OR 2.51, CI (1.37–4.61), p = 0.003,
respectively]. However, lower alkaline phosphatase levels
were associated with a lower OR of having type 2 diabetes
mellitus [OR 0.28, CI (0.15–0.52), p\0.0001] in regression
analysis. No significant difference was found between
serum osteocalcin levels of those with and without metabolic
syndrome. Among the metabolic syndrome components,
low osteocalcin levels had significant associations
with elevated blood glucose [OR 1.89, CI (1.16–3.07),
p = 0.010] and elevated waist circumference [OR 2.53, CI
(1.13–5.67), p = 0.024] in multivariate analyses. In conclusion,
serum osteocalcin was independently associated
with glucose intolerance and abdominal obesity as the
components of metabolic syndrome and type 2 diabetes
mellitus in postmenopausal women. Since CrossLaps and
alkaline phosphatase levels were independently associated
with the presence of type 2 diabetes mellitus, the unique
contribution of osteocalcin in glucose metabolism could
not be concluded
A Randomized Trial of Sitagliptin and Spironolactone With Combination Therapy in Hospitalized Adults With COVID-19
COVID-19 may cause respiratory distress syndrome and death. Treatment of COVID-19 to prevent complications remains a priority.
Objective
Our investigation sought to determine whether combination of spironolactone and sitagliptin could reduce mortality for inpatients with SARS-CoV-2 infection.
Methods
This single-blind, 4-arm, prospective randomized clinical trial was conducted at Shiraz and Bushehr University of Medical Sciences hospitals between December 2020 and April 2021. We randomized hospitalized adult patients with COVID-19 pneumonia into 4 groups: control, combination therapy, sitagliptin add-on, or spironolactone add-on. The primary outcome was the clinical improvement of the patients in the hospital as measured on an 8-point numerical scale. The secondary outcomes included intubation, ICU admission, end organ damages, CT findings, and paraclinical information.
Results
A total of 263 admitted patients were randomly assigned to control group (87 patients), combination group (60 patients), sitagliptin group (66 patients), and spironolactone group (50 patients). There were no significant differences in baseline characteristics, except for higher age in control group. The intervention groups, especially combination therapy, had better clinical outcomes (clinical score on fifth day of admission: 3.11 ± 2.45 for controls, 1.33 ± 0.50 for combination, 1.68 ± 1.02 for sitagliptin, and 1.64 ± 0.81 for spironolactone; P = 0.004). However, the mortality rate was lower in patients who received spironolactone (21.84% control, 13.33% combination, 13.64% sitagliptin, 10.00% spironolactone; P = 0.275). Our intervention reduced lung infiltration but not the area of involvement in lungs.
Conclusion
Sitagliptin and spironolactone can potentially improve clinical outcomes of hospitalized COVID-19 patients
Short-course treatment in neurobrucellosis: A study in Iran
Neurobrucellosis is a rare neurological complication of brucellosis.
This report describes 19 patients of neurobrucellosis and they
accounted for 8% of all cases of brucellosis admitted to Shiraz
University Hospitals over a period of eight years. Headache, fever,
fatigue, drowsiness and neck stiffness were the common clinical
features. Cerebrospinal fluid (CSF) showed pleocytosis in 100%,
elevated protein levels in 89% and low glucose level in 47% of the
patients. All the patients improved with specific antibiotic treatment.
Of the 19 patients, 10 (52.5%) patients received treatment for 8 to 28
weeks. Duration of antibiotic treatment was: 8-14 weeks in 8 (42%)
patients; 24-28 weeks in 2 (10.5%) patients; 6 months in 7 (37%)
patients; 12 months in 1 (5.3%) patient; and 18 months in 1 (5.3%)
patient. Clinicians in endemic areas should consider the likelihood of
neurobrucellosis in patients with unexplained neurological and
psychiatric symptoms